DE10256507A1 - Use of emulsifier mixtures for the production of cosmetic products - Google Patents
Use of emulsifier mixtures for the production of cosmetic products Download PDFInfo
- Publication number
- DE10256507A1 DE10256507A1 DE2002156507 DE10256507A DE10256507A1 DE 10256507 A1 DE10256507 A1 DE 10256507A1 DE 2002156507 DE2002156507 DE 2002156507 DE 10256507 A DE10256507 A DE 10256507A DE 10256507 A1 DE10256507 A1 DE 10256507A1
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- DE
- Germany
- Prior art keywords
- alcohols
- oil
- acid
- branched
- fatty
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000003995 emulsifying agent Substances 0.000 title claims abstract description 60
- 239000000203 mixture Substances 0.000 title claims abstract description 45
- 239000002537 cosmetic Substances 0.000 title claims abstract description 22
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 7
- 239000012071 phase Substances 0.000 claims abstract description 61
- 239000008346 aqueous phase Substances 0.000 claims abstract description 6
- 239000003921 oil Substances 0.000 claims description 46
- 235000019198 oils Nutrition 0.000 claims description 45
- -1 fatty alcohol carbonates Chemical class 0.000 claims description 42
- 150000002148 esters Chemical class 0.000 claims description 36
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 30
- 239000000194 fatty acid Substances 0.000 claims description 30
- 229930195729 fatty acid Natural products 0.000 claims description 30
- 150000004665 fatty acids Chemical class 0.000 claims description 25
- 150000001298 alcohols Chemical class 0.000 claims description 24
- 125000004432 carbon atom Chemical group C* 0.000 claims description 22
- 150000001875 compounds Chemical class 0.000 claims description 21
- 150000002191 fatty alcohols Chemical class 0.000 claims description 21
- 239000000839 emulsion Substances 0.000 claims description 20
- 230000036961 partial effect Effects 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 150000002170 ethers Chemical class 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 5
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 5
- 150000007513 acids Chemical class 0.000 claims description 4
- 229930182470 glycoside Natural products 0.000 claims description 4
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- 239000008271 cosmetic emulsion Substances 0.000 claims description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 3
- 150000002338 glycosides Chemical class 0.000 claims description 3
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- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims 2
- 239000001569 carbon dioxide Substances 0.000 claims 1
- 229910002092 carbon dioxide Inorganic materials 0.000 claims 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 23
- 239000001993 wax Substances 0.000 description 21
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- 239000003205 fragrance Substances 0.000 description 17
- 235000002639 sodium chloride Nutrition 0.000 description 17
- 150000003839 salts Chemical class 0.000 description 15
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 11
- 229920001577 copolymer Polymers 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 10
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- 239000002304 perfume Substances 0.000 description 10
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- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 4
- ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 description 4
- UYWQUFXKFGHYNT-UHFFFAOYSA-N Benzylformate Chemical compound O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- 239000005792 Geraniol Substances 0.000 description 4
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- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 4
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- UUQHKWMIDYRWHH-UHFFFAOYSA-N Methyl beta-orcinolcarboxylate Chemical group COC(=O)C1=C(C)C=C(O)C(C)=C1O UUQHKWMIDYRWHH-UHFFFAOYSA-N 0.000 description 4
- YBGZDTIWKVFICR-JLHYYAGUSA-N Octyl 4-methoxycinnamic acid Chemical compound CCCCC(CC)COC(=O)\C=C\C1=CC=C(OC)C=C1 YBGZDTIWKVFICR-JLHYYAGUSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
- 239000006096 absorbing agent Substances 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 150000001299 aldehydes Chemical class 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
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- FQAZRHVERGEKOS-UHFFFAOYSA-N tripropan-2-yl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CC(C)OC(=O)CC(O)(C(=O)OC(C)C)CC(=O)OC(C)C FQAZRHVERGEKOS-UHFFFAOYSA-N 0.000 description 1
- ODHUFJLMXDXVRC-UHFFFAOYSA-N tripropyl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CCCOC(=O)CC(O)(C(=O)OCCC)CC(=O)OCCC ODHUFJLMXDXVRC-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Abstract
Beschrieben wird die Verwendung von Emulgatorengemischen zur Herstellung von kosmetischen Mitteln, die eine wässrige und eine nicht-wässrige Phase enthalten, wobei das Mittel eine Phaseninversionstemperatur (PIT) im Bereich von -5 DEG C bis 45 DEG C aufweist.The use of emulsifier mixtures for the production of cosmetic compositions is described, which contain an aqueous and a non-aqueous phase, the composition having a phase inversion temperature (PIT) in the range from -5 ° C. to 45 ° C.
Description
Die vorliegende Erfindung betrifft die Verwendung von Emulgatorenmischungen zur Herstellung von kosmetischen Mitteln.The present invention relates to the use of emulsifier mixtures for the production of cosmetic Means.
Eine Vielzahl von kosmetischen Mittel werden in Form von Emulsionen angeboten. Je nach Art der Formulierung liegt die Emulsion als Öl-in-Wasser (O/W) oder als Wasser-in-Öl-System (W/O) vor. Beide Systeme unterscheiden sich insbesondere in ihren sensorischen Eigenschaften. So werden OIW-Emulsionen eher als kühl empfunden, während W/O-Emulsionen einen wärmenden Effekt vermitteln.A variety of cosmetic products are offered in the form of emulsions. Depending on the type of formulation the emulsion lies as an oil-in-water (O / W) or as a water-in-oil system (W / O) before. Both systems differ in particular in their sensory properties. So OIW emulsions are perceived as cool, while W / O emulsions a warming Convey effect.
Bei bestimmten Anwendungen, insbesondere im Bereich der Hautpflege ist es aber gewünscht, dass eine Formulierung beide Effekte, in Abhängigkeit von den Wünschen der Kunden, aufweist.In certain applications, especially in the field of skin care, however, it is desirable that a formulation both effects, depending of the wishes the customer.
Die Aufgabe der vorliegenden Erfindung bestand daher darin, kosmetische Mittel bereit zustellen, die diesen Anforderungen genügen. Allerdings müssen derartige Mittel auch über eine ausreichende Lagerstabilität verfügen, um kommerzialisierbar zu sein.The object of the present invention was therefore to provide cosmetic products that this Requirements met. However, must such funds also about adequate storage stability feature, to be commercializable.
Es wurde gefunden, dass durch den Einsatz bestimmter Emulgatorensysteme Mittel erhalten werden können, die den Anforderungen genügen.It was found that by the Use of certain emulsifier systems means that can be obtained meet the requirements.
In einer ersten Ausführungsform betrifft die vorliegende Erfindung daher die Verwendung von Emulgatorengemischen zur Herstellung von kosmetisches Mitteln, die eine wässerige und eine nichtwässerige Phase enthalten, wobei das Mittel eine Phaseninversionstemperatur (PIT) im Bereich von -5°C bis 45 °C aufweist.In a first embodiment The present invention therefore relates to the use of emulsifier mixtures for the production of cosmetic products that have an aqueous and a non-aqueous one Contain phase, the agent having a phase inversion temperature (PIT) in the range of -5 ° C up to 45 ° C having.
Mittel im Sinne der vorliegenden Erfindung können also reversible den Phasenzustand wechseln, also als O/W oder W/O-Emulsion vorliegen, wobei sich entsprechend die sensorischen Eigenschaften mit ändern. Die Phasenänderung wird durch Temperaturänderungen hervorgerufen. Es ist daher beispielsweise möglich eine kühlende Sonnenschutzemulsion durch Abkühlung in eine wärmende hautpflegende Emulsion umzuwandeln. Diese Phasenänderung kann beim Kunden erfolgen, indem dieser das Mittel z.B. im Kühlschrank kühlt.Means within the meaning of the present Invention can so reversibly change the phase state, i.e. as an O / W or W / O emulsion are present, the sensory properties accordingly with change. The phase change is caused by temperature changes caused. A cooling sun protection emulsion is therefore possible, for example by cooling in a warming to convert skin-care emulsion. This phase change can take place at the customer by this means e.g. cools in the fridge.
Es ist an sich bekannt, dass sich stabile Wasser und Öl enthaltenden Emulsionen in unterschiedlichen Phasenzuständen befinden können. So kann eine feindisperse Öl-Phase in der homogenen Wasserphase verteilt vorliegen (O/W), oder umgekehrt, die feindisperse wässerige Phase liegt in der Öl-Phase dispergiert vor (W/O). Der Phasenübergang zwischen den beiden Zuständen kann reversibel sein und lässt sich beispielsweise durch die Temperatur steuern.It is known in itself that stable water and oil containing emulsions are in different phase states can. So a finely dispersed oil phase are distributed in the homogeneous water phase (O / W), or vice versa, the finely dispersed watery Phase is in the oil phase dispersed before (W / O). The phase transition between the two states can be reversible and leaves control themselves through temperature, for example.
Bevor auf die Einzelheiten der erfindungsgemäßen technischen Lehre eingegangen wird, seien zusammenfassend hier wesentliche einschlägige Literatur und Fachwissen zum Phänomen der temperaturabhängigen Phaseninversion und des zugehörigen Parameters PIT zitiert. Im Licht dieses der Allgemeinheit zugänglichen Grundwissens erschließt sich das Verständnis und die Möglichkeit zur Verwirklichung der erfindungsgemäßen Lehre. Eine sehr sorgfältige Darstellung der Phasengleichgewichte von 3-Komponenten-Systemen aus wässriger Phase/Ölphase/Surfactant (insbesondere nichtionische Emulgatoren/Emulgatorsysteme) findet sich in der Veröffentlichung K. SHINODA und N. KUNIEDA "Phase Properties of Emulsions: PIT and HLB" in "Encyclopedia of Emulsion Technology, 1983, Vol. 1, 337 bis 367. Die Verfasser beziehen in ihre Veröffentlichung insbesondere auch den einschlägigen umfangreichen druckschriftlichen Stand der Technik ein, wobei zum Verständnis der im nachfolgenden gegebenen erfindungsgemäßen Lehre insbesondere das Wissen zur Temperaturabhängigkeit der Phaseninversion solcher Emulgatoren enthaltenden Öl/Wasser-Systeme von Bedeutung ist. Die zitierte Veröffentlichung SHINODA et al. geht auf diesen Temperaturparameter und die durch seine Variation ausgelösten Effekte im Mehrphasensystem ausführlich ein. Dargestellt sind für fließfähige Stoffgemische auf Basis der 3-Komponenten-Systeme Öl/Wasserl-Emulgator insbesondere die Abhängigkeit der sich jeweils einstellenden Phasengleichgewichtszustände von der Temperatur des Mehrkomponentensystems. Der im vergleichsweise niedrigeren Temperaturbereich stabile Zustand der O/W-Emulsion mit einer dispersen Ölphase in der geschlossenen Wasserphase geht bei Temperatursteigerung in den Bereich der Phaseninversion – PIT bzw. Bereich der "Mittelphase" – über. Bei weiterer Temperatursteigerung invertiert das Mehrkomponentensystem zum stabilen W/O-Invertzustand, in dem in der geschlossenen Ölphase die Wasserphase jetzt dispergiert vorliegt.Before going to the details of the technical invention Teaching is summarized here are essential relevant literature and expertise on the phenomenon the temperature-dependent Phase inversion and the associated Parameters PIT cited. In the light of this accessible to the general public Develops basic knowledge yourself understanding and the possibility to implement the teaching of the invention. A very careful presentation the phase equilibria of 3-component systems from aqueous Phase / oil phase / surfactant (especially non-ionic emulsifiers / emulsifier systems) themselves in the publication K. SHINODA and N. KUNIEDA "phase Properties of Emulsions: PIT and HLB "in" Encyclopedia of Emulsion Technology, 1983, vol. 1, 337 to 367. The authors relate to their publication especially the relevant ones extensive printed state of the art, whereby at understanding the teaching according to the invention given below in particular that Knowledge of temperature dependence the phase inversion of such oil / water systems containing emulsifiers Meaning is. The cited publication SHINODA et al. goes through this temperature parameter and the its variation triggered Effects in the multi-phase system in detail on. Are shown for flowable mixtures of substances based on the 3-component oil / water emulsifier systems in particular the dependence of the phase equilibrium states of the temperature of the multi-component system. The one in comparison lower temperature range with stable state of the O / W emulsion a disperse oil phase in the closed water phase goes in when the temperature rises the area of phase inversion - PIT or area of the "middle phase" - about. When the temperature increases further inverts the multi-component system to a stable W / O invert state, in the in the closed oil phase the water phase is now dispersed.
Die Bestimmung dieser unterschiedlichen Phasenbereiche und insbesondere gerade auch die Bestimmung der im jeweiligen System gegebenen (Mikroemulsions-)Mittelphase ist in zweifacher Weise möglich, wobei diese beiden Möglichkeiten zweckmäßigerweise miteinander verbunden werden:Determining these different Phase ranges and especially the determination of the im given system (microemulsion) middle phase is in possible in two ways taking these two options expediently be connected:
- a) Bestimmung der Temperaturabhängigkeit und die damit verbundene Phasenverschiebung durch experimentelles Ausprüfen des jeweiligen Systems, insbesondere mittels Leitfähigkeitsbestimmung.a) Determination of the temperature dependence and the associated phase shift through experimental Debugging of the respective system, in particular by means of conductivity determination.
- b) Vorab besteht aufgrund des heutigen Fachwissens die Möglichkeit zur rechnerischen Ermittlung der PIT des jeweils betroffenen Systems.b) In advance, based on today's specialist knowledge, there is the possibility of calculating the PIT by calculation of the affected system.
Grundsätzlich gilt: Das Phänomen der Phaseninversion und der zugehörigen Phaseninversionstemperatur (PIT) findet innerhalb eines Temperaturbereiches statt, der seinerseits mit einer Untergrenze sich gegen den O/W-Emulsionszustand und mit seiner Obergrenze gegen den W/O-Invertemulsionszustand abgrenzt. Die experimentelle Ausprüfung des jeweiligen Systems, insbesondere durch Leitfähigkeitsbestimmung bei ansteigender und/oder abfallender Temperatur, gibt Maßzahlen für die jeweilige PIT-Untergrenze und PIT-Obergrenze, wobei hier nochmals leichte Verschiebungen vorliegen können, wenn die Leitfähigkeitsprüfung einmal in aufsteigendem Temperaturast und zum anderen im abfallenden Temperaturast bestimmt werden. Die Phaseninversionstemperatur (PIT) oder besser gesagt der PIT-Bereich zeigt insoweit Übereinstimmung mit der Definition der zuvor erläuterten WINSOR III-(Mikroemulsions-)Mittelphase. Dabei gilt jedoch: Der Abstand zwischen der PIT-Untergrenze (Abgrenzung gegen O/W-) und der PIT-Obergrenze (Abgrenzung gegen W/O-Invert-) ist in aller Regel ein steuerbarer und durch Wahl geeigneter Emulgatorkomponenten bzw. -systeme vergleichsweise beschränkter Temperaturbereich. Häufig sind hier Temperaturbereiche gegeben, die als Differenzwert weniger als 20 bis 30°C, insbesondere nicht mehr als 10 bis 15°C, ergeben. Für bestimmte Ausführungsformen kann es aber durchaus interessant sein, mit vergleichsweise breiten Temperaturbereichen für die Phaseninversion zu arbeiten.Basically, the phenomenon of Phase inversion and the associated Phase inversion temperature (PIT) takes place within a temperature range instead, which in turn has a lower limit against the O / W emulsion state and delimits with its upper limit against the W / O invert emulsion state. The experimental testing of the respective system, in particular by determining the conductivity with increasing and / or falling temperature, gives measures for the respective lower PIT limit and PIT upper limit, with slight shifts again can, once the conductivity test in the ascending temperature branch and on the other hand in the falling temperature branch be determined. The phase inversion temperature (PIT) or better said the PIT area shows agreement with the definition the previously explained WINSOR III (microemulsion) middle phase. However, the following applies: the distance between the PIT lower limit (delimitation against E / W-) and the PIT upper limit (Differentiation from W / O-Invert-) is usually a controllable one and comparatively by choosing suitable emulsifier components or systems limited Temperature range. Frequently there are temperature ranges that are less than the difference value than 20 to 30 ° C, in particular not more than 10 to 15 ° C, result. For certain embodiments but it can be quite interesting, with comparatively broad ones Temperature ranges for the phase inversion to work.
Die rechnerische Ermittlung der PIT des jeweils betroffenen Systems gemäß b) führt demgegenüber nicht zur exakten Bestimmung der zuvor erwähnten Temperaturgrenzwerte des jeweiligen PIT-Bereiches, sondern zu einem Zahlenwert, der in der Größenordnung des in der Praxis dann tatsächlich auftretenden PIT-Bereiches liegt. Damit wird verständlich, daß die Kombination der Ermittlungen zur Phasenverschiebung gemäß a) und b) für die Praxis zweckmäßig sein kann.The mathematical determination of the PIT the system concerned in accordance with b) does not lead to this for the exact determination of the aforementioned temperature limit values of the respective PIT area, but to a numerical value that is of the order of magnitude in practice then actually occurring PIT range. This makes it understandable that the Combination of the phase shift determinations according to a) and b) for the practice may be appropriate can.
Die experimentelle Bestimmung des Temperaturbereiches zur Phaseninversion durch Leitfähigkeitsmessungen ist in dem hier einschlägigen druckschriftlichen Stand der Technik ausführlich beschrieben. Insoweit kann darauf Bezug genommen werden. Die unter den Phaseninversions- Temperaturbereich abgekühlten O/W-Emulsionen zeigen bei der Leitfähigkeitsbestimmung eine elektrische Leitfähigkeit von über 1 mSiemens pro cm (mS/cm). Durch langsames Erwärmen unter vorgegebenen Programmbedingungen wird ein Leitfähigkeitsdiagramm erstellt. Der Temperaturbereich, innerhalb dessen die Leitfähigkeit auf Werte unterhalb 0,1 mS/cm abfällt, wird als Phaseninversions-Temperaturbereich notiert. Für die Zwecke der erfindungsgemäßen Lehre ist es zweckmäßig ein entsprechendes Leitfähigkeitsdiagramm auch auf dem abfallenden Temperaturast zu erstellen, bei dem die Leitfähigkeit an einem Mehrkomponentengemisch ermittelt wird, das zunächst auf Temperaturen oberhalb des Phaseninversions-Temperaturbereichs erhitzt worden ist und dann in vorbestimmter Weise gekühlt wird. Die hier bestimmten oberen und unteren Grenzwerte für den Phaseninversions-Temperaturbereich müssen nicht voll identisch sein mit den entsprechenden Werten des zuvor geschilderten Bestimmungsabschnittes mit ansteigender Temperatur des Mehrkomponentengemisches. In der Regel sind allerdings die jeweiligen Grenzwerte doch so dicht beieinander gelagert, daß für das großtechnische Arbeiten mit vereinheitlichten Maßzahlen – insbesondere durch Mittelwertbildung der jeweils zueinander gehörigen Grenzwerte – gearbeitet werden kann. Aber auch für den Fall, daß hier stärkere Differenzierungen der Grenzwerte des Phaseninversions-Temperaturbereiches einmal bei der Bestimmung in ansteigender Temperatur und zum anderen in der Bestimmung bei abfallender Temperatur gemessen werden, ist die Durchführbarkeit der im nachfolgenden im einzelnen geschilderten technischen Lehre aus den hier eingesetzten Arbeitsprinzipien sichergestellt. Zur Minderung des experimentellen Arbeitsaufwandes kann die rechnerische Ermittlung der PIT des jeweils betroffenen Mehrkomponentensystems zweckmäßig sein. Insbesondere gilt das aber auch für potentielle Optimierungen in der Auswahl der Emulgatoren beziehungsweise Emulgatorsysteme und ihrer Anpassung an die durch sonstige Überlegungen zum technischen Handeln vorgegebene Auswahl und Abmischung von wässriger Phase einerseits und Typ der Ölphase andererseits. Basierend auf diesen Grundkenntnissen wird es möglich, für die jeweils zum praktischen Einsatz beabsichtigten Komponenten – insbesondere die Ölphase und zugehörige Emulgatoen/Emulgatorsysteme nach Art und Menge – vorab Mischungen und Mischungsverhältnisse zu bestimmen, deren PIT in dem erfindungsgemäß angestrebten Temperaturbereich liegt. Hieraus ergibt sich ein erster sinnvoller Ansatz zur Durchführung experimenteller Arbeiten im Sinne der Ermittlungsmethode zu a). Über die rechnerische Ermittlung der PIT hinausgehend kann insbesondere der Bereich der Bildung der Mittelphase mit ihrer Temperaturuntergrenze und insbesondere ihrer Temperaturobergrenze bestimmt werden.The experimental determination of the Temperature range for phase inversion through conductivity measurements is relevant here The state of the art in writing is described in detail. in this respect can be referred to. The under the phase inversion temperature range cooled O / W emulsions show when determining conductivity an electrical conductivity from above 1 mSiemens per cm (mS / cm). By slowly warming up under specified program conditions becomes a conductivity diagram created. The temperature range within which the conductivity drops to values below 0.1 mS / cm is called the phase inversion temperature range written down. For the purposes of the teaching of the invention it is appropriate corresponding conductivity diagram also to create on the falling temperature branch, at which the conductivity is determined on a multi-component mixture, which is initially based on Temperatures heated above the phase inversion temperature range has been and then cooled in a predetermined manner. The ones determined here upper and lower limits for the phase inversion temperature range have to not be completely identical to the corresponding values of the previous one described determination section with increasing temperature of the multi-component mixture. As a rule, however, are the respective ones Limit values stored so close together that for large-scale Working with standardized measures - especially by averaging that belong to each other Limit values - worked can be. But also for the case here more Differentiations of the limit values of the phase inversion temperature range on the one hand when determining in increasing temperature and on the other measured in the determination at a falling temperature the feasibility the technical teaching described in detail below ensured from the working principles used here. to Reduction of the experimental workload can be the computational Determination of the PIT of the multi-component system concerned be appropriate. In particular, this also applies to potential optimizations in the selection of emulsifiers or emulsifier systems and adapting them to other technical considerations Act predetermined selection and mixing of aqueous phase on the one hand and Oil phase type on the other hand. Based on this basic knowledge, it becomes possible for each Components intended for practical use - in particular the oil phase and related Emulsifiers / emulsifier systems according to type and quantity - in advance mixtures and mixing ratios to determine their PIT in the temperature range sought according to the invention lies. This gives a first sensible approach to performing experimental Work in the sense of the investigation method for a). About the calculation The PIT can go beyond the area of education of the Middle phase with its lower temperature limit and especially yours Upper temperature limit can be determined.
Diese oben geschilderten Eigenschaften
von wässerigen
Emulsionen werden auch bereits in einigen Bereichen der Technik
genutzt. So beschreibt die
Bei kosmetischen Mitteln sind andere Inhaltsstoffe betroffen und weiterhin werden andere Maßstäbe in Bezug auf die Stabilität angewendet . Ein kosmetische Mittel muss, ohne weitere Eingriffe teilweise über Jahre stabil bleiben, um verkauft werden zu können. Eine einfache Übertragung der Lehre der oben zitierten Schrift auf die Herstellung kosmetischer Mittel war daher nicht möglich.With cosmetic products there are others Ingredients affected and continue to apply different standards on stability applied . A cosmetic product needs no further intervention partially over Stay stable for years to be sold. An easy transfer the teaching of the scripture cited above on the production of cosmetic So funds were not possible.
Bei kosmetischen Mitteln handelt es sich, gemäß der Definition der CIDESCO, um Mittel, die eingesetzt werden, um eine Verschönerung der Haut, des Gesichts und des Körpers zu Erreichen. Demnach versteht man unter Kosmetik alle Maßnahmen an der Haut, ihren Anhangsorganen und den wahrnehmbaren Schleimhäuten zur Reinigung (einschließlich der Desodorierung und Antitranspiration), zur erhaltenden, vorbeugenden und verbessernden Pflege (einschließlich der Zahn- und Mundpflege), zur Verschönerung, Dekorierung od. Färbung (einschließlich der Verw. von Parfüms) sowie die plast. Chirurgie. Je nach Applikationszweck enthalten die kosmetischen Formulierungen eine Reihe weiterer Hilfs- und Zusatzstoffe, wie beispielsweise Tenside, weitere Ölkörper, Emulgatoren, Perlglanzwachse, Konsistenzgeber, Verdickungsmittel, Überfettungsmittel, Stabilisatoren, Polymere, Siliconverbindungen, Fette, Wachse, Lecithine, Phospholipide, biogene Wirkstoffe, UV-Lichtschutzfaktoren, Antioxidantien, Deodorantien, Antitranspirantien, Antischuppenmittel, Filmbildner, Quellmittel, Insektenrepellentien, Selbstbräuner, Tyrosinaseinhibitoren (Depigmentierungsmittel), Hydrotrope, Solubilisatoren, Konservierungsmittel, Parfümöle, Farbstoffe etc., die nachstehend exemplarisch aufgelistet sind.Trade in cosmetic products it, according to the definition the CIDESCO, to funds that are used to beautify the Skin, face and body to reach. Accordingly, cosmetics mean all measures on the skin, its appendix organs and the noticeable mucous membranes Cleaning (including deodorization and antiperspiration), for preservative, preventive and improving care (including dental and oral care), for embellishment, Decoration or coloring (including the use of perfumes) as well as the plast. Surgery. Depending on the application purpose included the cosmetic formulations contain a number of other auxiliaries and additives, such as surfactants, other oil bodies, emulsifiers, pearlescent waxes, Consistency enhancers, thickeners, superfatting agents, stabilizers, Polymers, silicone compounds, fats, waxes, lecithins, phospholipids, biogenic agents, UV light protection factors, antioxidants, deodorants, Antiperspirants, antidandruff agents, film formers, swelling agents, Insect repellents, self-tanners, Tyrosinase inhibitors (depigmenting agents), hydrotropes, solubilizers, Preservatives, perfume oils, dyes etc., which are listed below as examples.
Ölkörperoil body
Als zusätzliche Ölkörper kommen weitere Verbindungen in Frage, beispielsweise Guerbetalkohole auf Basis von Fettalkoholen mit 6 bis 18, vorzugsweise 8 bis 10 Kohlenstoffatomen, Ester von linearen C6-C22-Fettsäuren mit linearen oder verzweigten C6-C22-Fettalkoholen bzw. Ester von verzweigten C6-C13-Carbonsäuren mit linearen oder verzweigten C6-C22-Fettalkoholen, wie z. B. Myristylmyristat, Myristylpalmitat, Myristylstearat, Myristylisostearat, Myristyloleat, Myristylbehenat, Myristylerucat, Cetylmyristat, Cetylpalmitat, Cetylstearat, Cetylisostearat, Cetyloleat, Cetylbehenat, Cetylerucat, Stearylmyristat, Stearylpalmitat, Stearylstearat, Stearylisostearat, Stearyloleat, Stearylbehenat, Stearylerucat, Isostearylmyristat, Isostearylpalmitat, Isostearylstearat, Isostearylisostearat, Isostearyloleat, Isostearylbehenat, Isostearyloleat, Oleylmyristat, Oleylpalmitat, Oleylstearat, Oleylisostearat, Oleyloleat, Oleylbehenat, Oleylerucat, Behenylmyristat, Behenylpalmitat, Behenylstearat, Behenylisostearat, Behenyloleat, Behenylbehenat, Behenylerucat, Erucylmyristat, Erucylpalmitat, Erucylstearat, Erucylisostearat, Eru-cyloleat, Erucylbehenat und Erucylerucat. Daneben eignen sich Ester von linearen C6-C22-Fettsäuren mit verzweigten Alkoholen, insbesondere 2-Ethylhexanol, Ester von C18-C38-Alkylhydroxycarbonsäuren mit linearen oder verzweigten C6-C22-Fettalkoholen, insbesondere Dioctyl Malate, Ester von linearen und/oder verzweigten Fettsäuren mit mehrwertigen Alkoholen (wie z. B. Propylenglycol, Dimerdiol oder Trimertriol) und/oder Guerbetalkoholen, Triglyceride auf Basis C6-C10-Fettsäuren, flüssige Mono-/Di-/Triglyceridmischungen auf Basis von C6-C18-Fettsäuren, Ester von C6-C22-Fettalkoholen und/oder Guerbetalkoholen mit aromatischen Carbonsäuren, insbesondere Benzoesäure, Ester von C2-C22-Dicarbonsäuren mit linearen oder verzweigten Alkoholen mit 1 bis 22 Kohlenstoffatomen oder Polyolen mit 2 bis 10 Kohlenstoffatomen und 2 bis 6 Hydroxylgruppen, pflanzliche Öle, verzweigte primäre Alkohole, substituierte Cyclohexane, lineare und verzweigte C6-C22-Fettalkoholcarbonate, wie z. B. Dicaprylyl Carbonate (Cetiol® CC), Guerbetcarbonate auf Basis von Fettalkoholen mit 6 bis 18, vorzugsweise 8 bis 10 C Atomen, Ester der Benzoesäure mit linearen und/oder verzweigten C6-C22-Alkoholen (z. B. Finsolv® TN), lineare oder verzweigte, symmetrische oder unsymmetrische Dialkylether mit 6 bis 22 Kohlenstoffatomen pro Alkylgruppe, wie z. B. Dicaprylyl Ether (Cetiol® OE), Ringöffnungsprodukte von epoxidierten Fettsäureestern mit Polyolen, Siliconöle (Cyclomethicone, Siliciummethicontypen u.a.) und/oder aliphatische bzw. naphthenische Kohlenwasserstoffe, wie z. B. wie Squalan, Squalen oder Dialkylcyclohexane in Betracht.Additional compounds which may be used are additional compounds, for example Guerbet alcohols based on fatty alcohols having 6 to 18, preferably 8 to 10 carbon atoms, esters of linear C 6 -C 22 fatty acids with linear or branched C 6 -C 22 fatty alcohols or esters of branched C 6 -C 13 carboxylic acids with linear or branched C 6 -C 22 fatty alcohols, such as. B. myristyl myristate, myristyl palmitate, myristyl stearate, Myristylisostearat, myristyl, Myristylbehenat, Myristylerucat, cetyl myristate, cetyl palmitate, cetyl stearate, Cetylisostearat, cetyl oleate, cetyl behenate, Cetylerucat, Stearylmyristat, stearyl palmitate, stearyl stearate, Stearylisostearat, stearyl oleate, stearyl behenate, Stearylerucat, isostearyl, isostearyl palmitate, Isostearylstearat, isostearyl isostearate, Isostearyloleat, isostearyl behenate, Isostearyloleat, oleyl, oleyl palmitate, oleyl stearate, oleyl isostearate, oleate, Oleylbehenat, oleyl, behenyl myristate, behenyl, behenyl, Behenylisostearat, behenyl oleate, behenyl, erucyl, erucyl, erucyl, erucyl, erucyl, Eru-cyloleat, erucyl and erucylerucate. In addition, esters of linear C 6 -C 22 fatty acids with branched alcohols, in particular 2-ethylhexanol, esters of C 18 -C 38 alkylhydroxycarboxylic acids with linear or branched C 6 -C 22 fatty alcohols, in particular dioctyl malates, esters of linear and / or branched fatty acids with polyhydric alcohols (such as propylene glycol, dimer diol or trimer triol) and / or Guerbet alcohols, triglycerides based on C 6 -C 10 fatty acids, liquid mono- / di- / triglyceride mixtures based on C 6 - C 18 fatty acids, esters of C 6 -C 22 fatty alcohols and / or Guerbet alcohols with aromatic carboxylic acids, in particular benzoic acid, esters of C 2 -C 22 dicarboxylic acids with linear or branched alcohols with 1 to 22 carbon atoms or polyols with 2 to 10 Carbon atoms and 2 to 6 hydroxyl groups, vegetable oils, branched primary alcohols, substituted cyclohexanes, linear and branched C 6 -C 22 fatty alcohol carbonates, such as. B. dicaprylyl carbonates (Cetiol ® CC), Guerbet carbonates based on fatty alcohols with 6 to 18, preferably 8 to 10 C atoms, esters of benzoic acid with linear and / or branched C 6 -C 22 alcohols (e.g. Finsolv ® TN), linear or branched, symmetrical or asymmetrical dialkyl ethers having 6 to 22 carbon atoms per alkyl group, such as. B. dicaprylyl ether (Cetiol ® OE), ring opening products of epoxidized fatty acid esters with polyols, silicone oils (cyclomethicones, silicon methicone types, etc.) and / or aliphatic or naphthenic hydrocarbons, such as. B. as squalane, squalene or dialkylcyclohexane.
Fette und WachseFats and waxes
Fette und Wachse werden den Körperpflegeprodukten als Pflegestoffe zugesetzt und auch, um die Konsistenz der Kosmetika zu erhöhen. Typische Beispiele für Fette sind Glyceride, d. h. feste oder flüssige pflanzliche oder tierische Produkte, die im wesentlichen aus gemischten Glycerinestern höherer Fettsäuren bestehen. Auch Fettsäurepartialglyceride, d. h. technische Mono- und/oder Diester des Glycerins mit Fettsäuren mit 12 bis 18 Kohlenstoffatomen wie etwa Glycerinmono/dilaurat, -palmitat oder -stearat kommen hierfür in Frage. Als Wachse kommen u. a. natürliche Wachse, wie z. B. Candelillawachs, Carnaubawachs, Japanwachs, Espartograswachs, Korkwachs, Guarumawachs, Reiskeimölwachs, Zuckerrohrwachs, Ouricurywachs, Montanwachs, Bienenwachs, Schellackwachs, Walrat, Lanolin (Wollwachs), Bürzelfett, Ceresin, Ozokerit (Erdwachs), Petrolatum, Paraffinwachse, Mikrowachse; chemisch modifizierte Wachse (Hartwachse), wie z. B. Montanesterwachse, Sasolwachse, hydrierte Jojobawachse sowie synthetische Wachse, wie z. B. Polyalkylenwachse und Polyethylenglycolwachse in Frage. Neben den Fetten kommen als Zusatzstoffe auch fettähnliche Substanzen, wie Lecithine und Phospholipide in Frage. Unter der Bezeichnung Lecithine versteht der Fachmann diejenigen Glycero-Phospholipide, die sich aus Fettsäuren, Glycerin, Phosphorsäure und Cholin durch Veresterung bilden. Lecithine werden in der Fachwelt daher auch häufig als Phosphatidylcholine (PC) bezeichnet. Als Beispiele für natürliche Lecithine seien die Kephaline genannt, die auch als Phosphatidsäuren bezeichnet werden und Derivate der 1,2-Diacyl-sn-glycerin-3-phosphorsäuren darstellen. Dem gegenüber versteht man unter Phospholipiden gewöhnlich Mono- und vorzugsweise Diester der Phosphorsäure mit Glycerin (Glycerinphosphate), die allgemein zu den Fetten gerechnet werden. Daneben kommen auch Sphingosine bzw. Sphingolipide in Frage.Fats and waxes are added to the personal care products as care substances and also to increase the consistency of the cosmetics. Typical examples of fats are glycerides, ie solid or liquid vegetable or animal products which essentially consist of mixed glycerol esters of higher fatty acids. Fatty acid partial glycerides, ie technical mono- and / or diesters of glycerol with fatty acids with 12 to 18 carbon atoms, such as glycerol mono / dilaurate, palmitate or stearate, are also suitable for this. Natural waxes such as z. B. candelilla wax, carnauba wax, japan wax, esparto grass wax, cork wax, guaruma wax, rice germ oil wax, sugar cane wax, ouricury wax, montan wax, beeswax, shellac wax, walnut, lanolin (wool wax), pretzel fat, ceresin, ozokerite (earth wax), petrolatum, paraffin waxes, micro waxes; chemically modified waxes (hard waxes), such as. B. Montanester waxes, Sasol waxes, hydrogenated jojoba waxes and synthetic waxes, such as. B. polyalkylene waxes and polyethylene glycol waxes in question. In addition to fats, fat-like substances such as lecithins and phospholipids can also be used as additives. The person skilled in the art understands the term lecithins as those glycerophospholipids which are formed from fatty acids, glycerol, phosphoric acid and choline by esterification. Lecithins are therefore often referred to in the professional world as phosphatidylcholines (PC). Examples of natural lecithins are the cephalins, which are also referred to as phosphatidic acids and are derivatives of 1,2-diacyl-sn-glycerol-3-phosphoric acids. In contrast, phospholipids are usually understood to be mono- and preferably diesters of phosphoric acid with glycerol (glycerol phosphates), which are generally classed as fats. In addition, sphingosines or sphingolipids are also suitable.
Perlglanzwachsepearlescent
Als Perlglanzwachse kommen beispielsweise in Frage: Alkylenglycolester, speziell Ethylenglycoldistearat; Fettsäurealkanolamide, speziell Kokosfettsäurediethanolamid; Partialglyceride, speziell Stearinsäuremonoglycerid; Ester von mehrwertigen, gegebenenfalls hydroxy-substituierte Carbonsäuren mit Fettalkoholen mit 6 bis 22 Kohlenstoffatomen, speziell langkettige Ester der Weinsäure; Fettstoffe, wie beispielsweise Fettalkohole, Fettketone, Fettaldehyde, Fettether und Fettcarbonate, die in Summe mindestens 24 Kohlenstoffatome aufweisen, speziell Lauron und Distearylether; Fettsäuren wie Stearinsäure, Hydroxystearinsäure oder Behensäure, Ringöffnungsprodukte von Olefinepoxiden mit 12 bis 22 Kohlenstoffatomen mit Fettalkoholen mit 12 bis 22 Kohlenstoffatomen und/oder Polyolen mit 2 bis 15 Kohlenstoffatomen und 2 bis 10 Hydroxylgruppen sowie deren Mischungen.For example, come as pearlescent waxes in question: alkylene glycol esters, especially ethylene glycol distearate; fatty acid, especially coconut fatty acid diethanolamide; Partial glycerides, especially stearic acid monoglyceride; Esters of polyvalent, optionally hydroxy-substituted carboxylic acids with Fatty alcohols with 6 to 22 carbon atoms, especially long-chain ones Esters of tartaric acid; Fatty substances, such as fatty alcohols, fatty ketones, fatty aldehydes, Fatty ethers and fatty carbonates, which have a total of at least 24 carbon atoms, especially lauron and distearyl ether; Fatty acids such as stearic acid, hydroxystearic acid or behenic, Ring opening products of olefin epoxides with 12 to 22 carbon atoms with fatty alcohols with 12 to 22 carbon atoms and / or polyols with 2 to 15 carbon atoms and 2 to 10 hydroxyl groups and mixtures thereof.
Konsistenzgeber und VerdickungsmittelConsistency agents and thickeners
Als weitere Konsistenzgeber kommen in erster Linie Fettalkohole oder Hydroxyfettalkohole mit 12 bis 22 und vorzugsweise 16 bis 18 Kohlenstoffatomen und daneben Partialglyceride, Fettsäuren oder Hydroxyfettsäuren in Betracht. Bevorzugt ist eine Kombination dieser Stoffe mit Alkyloligoglucosiden und/oder Fettsäure-N-methylglucamiden gleicher Kettenlänge und/oder Polyglycerinpoly-12-hydroxystearaten. Geeignete Verdickungsmittel sind beispielsweise Aerosil-Typen (hydrophile Kieselsäuren), Polysaccharide, insbesondere Xanthan-Gum, Guar-Guar, Agar-Agar, Alginate und Tylosen, Carboxymethylcellulose und Hydroxyethyl- und Hydroxypropylcellulose, ferner höhermolekulare Polyethylenglycolmono- und -diester von Fettsäuren, Polyacrylate, (z. B. Carbopole® und Pemulen-Typen von Goodrich; Synthalene® von Sigma; Keltrol-Typen von Kelco; Sepigel-Typen von Seppic; Salcare-Typen von Allied Colloids), Polyacrylamide, Polymere, Polyvinylalkohol und Polyvinylpyrrolidon. Als besonders wirkungsvoll haben sich auch Bentonite, wie z. B. Bentone® Gel VS-5PC (Rheox) erwiesen, bei dem es sich um eine Mischung aus Cyclopentasiloxan, Disteardimonium Hectorit und Propylencarbonat handelt. Weiter in Frage kommen Tenside, wie beispielsweise ethoxylierte Fettsäureglyceride, Ester von Fettsäuren mit Polyolen wie beispielsweise Pentaerythrit oder Trimethylolpropan, Fettalkoholethoxylate mit eingeengter Homologenverteilung oder Alkyloligoglucoside sowie Elektrolyte wie Kochsalz und Ammoniumchlorid.Other possible consistency agents are primarily fatty alcohols or hydroxy fatty alcohols with 12 to 22 and preferably 16 to 18 carbon atoms and, in addition, partial glycerides, fatty acids or hydroxy fatty acids. A combination of these substances with alkyl oligoglucosides and / or fatty acid N-methylglucamides of the same chain length and / or polyglycerol poly-12-hydroxystearates is preferred. Suitable thickeners are, for example, Aerosil types (hydrophilic silicas), polysaccharides, in particular xanthan gum, guar guar, agar agar, alginates and tyloses, carboxymethyl cellulose and hydroxyethyl and hydroxypropyl cellulose, as well as higher molecular weight polyethylene glycol mono- and diesters of fatty acids, polyacrylates, (. eg Carbopol ® and Pemulen grades from Goodrich; Synthalens ® from Sigma; Keltrol grades from Kelco; Sepigel grades from Seppic; Salcare grades from Allied Colloids), polyacrylamides, polymers, polyvinyl alcohol and polyvinyl pyrrolidone. Bentonites, such as, for example, have also proven particularly effective. B. Bentone ® Gel VS-5PC (Rheox), which is a mixture of cyclopentasiloxane, disteardimonium hectorite and propylene carbonate. Surfactants such as, for example, ethoxylated fatty acid glycerides, esters of fatty acids with polyols such as, for example, pentaerythritol or trimethylolpropane, fatty alcohol ethoxylates with a narrow homolog distribution or alkyl oligoglucosides and electrolytes such as sodium chloride and ammonium chloride are also suitable.
Überfettungsmittelsuperfatting
Als Überfettungsmittel können Substanzen wie beipielsweise Lanolin und Lecithin sowie polyethoxylierfe oder acylierte Lanolin- und Lecithinderivate, Polyolfettsäureester, Monoglyceride und Fettsäurealkanolamide verwendet werden, wobei die letzteren gleichzeitig als Schaumstabilisatoren dienen.Substances can be used as superfatting agents such as lanolin and lecithin and polyethoxylierfe or acylated lanolin and lecithin derivatives, polyol fatty acid esters, Monoglycerides and fatty acid alkanolamides are used, the latter at the same time as foam stabilizers serve.
Stabilisatorenstabilizers
Als Stabilisatoren können Metallsalze von Fettsäuren, wie z. B. Magnesium-, Aluminium- und/oder Zinkstearat bzw. -ricinoleat eingesetzt werden.Metal salts can be used as stabilizers of fatty acids, such as B. magnesium, aluminum and / or zinc stearate or ricinoleate be used.
Polymerepolymers
Geeignete kationische Polymere sind beispielsweise kationische Cellulosederivate, wie z. B. eine quaternierte Hydroxyethylcellulose, die unter der Bezeichnung Polymer JR 400® von Amerchol erhältlich ist, kationische Stärke, Copolymere von Diallylammoniumsalzen und Acrylamiden, quaternierte Vinylpyrrolidon/Vinylimidazol-Polymere, wie z. B. Luviquat® (BASF), Kondensationsprodukte von Polyglycolen und Aminen, quaternierte Kollagenpolypeptide, wie beispielsweise Lauryldimonium Hydroxypropyl Hydrolyzed Collagen (Lamequat®L/Grünau), quaternierte Weizenpolypeptide, Polyethylenimin, kationische Siliconpolymere, wie z. B. Amodimethicone, Copolymere der Adipinsäure und Dimethylaminohydroxypropyldiethylentriamin (Cartaretine®/Sandoz), Copolymere der Acrylsäure mit Dimethyl-diallylammoniumchlorid (Merquat® 550/Chemviron), Polyaminopolyamide sowie deren vernetzte wasserlöslichen Polymere, kationische Chitinderivate wie beispielsweise quaterniertes Chitosan, gegebenenfalls mikrokristallin verteilt, Kondensationsprodukte aus Dihalogenalkylen, wie z. B. Dibrombutan mit Bisdialkylaminen, wie z. B. Bis-Dimethylamino-1,3-propan, kationischer Guar-Gum, wie z. B. Jaguar® CBS, Jaguar® C-17, Jaguar® C-16 der Firma Celanese, quaternierte Ammoniumsalz-Polymere, wie z. B. Mirapol® A-15, Mirapol® AD-1, Mirapol® AZ-1 der Firma Miranol.Suitable cationic polymers are, for example, cationic cellulose derivatives, such as. B. a quaternized hydroxyethyl cellulose, which is available under the name Polymer JR 400 ® from Amerchol, cationic starch, copolymers of diallylammonium salts and acrylamides, quaternized vinylpyrrolidone / vinylimidazole polymers, such as. B. Luviquat ® (BASF), condensation products of polyglycols and amines, quaternized collagen polypeptides, such as lauryldimonium hydroxypropyl hydrolyzed collagen (Lame quat ® L / Grünau), quaternized wheat polypeptides, polyethyleneimine, cationic silicone polymers such as B. amodimethicones, copolymers of adipic acid and dimethylaminohydroxypropyldiethylenetriamine (Cartaretine ® / Sandoz), copolymers of acrylic acid with dimethyldiallylammonium chloride (Merquat ® 550 / Chemviron), polyaminopolyamides and their crosslinked water-soluble polymers, cationic chitin derivatives, such as quaternized, quaternized chitinated products, for example, quaternized chitinated products, such as quaternized chitinated products, such as quaternized chitinated products, such as quaternized chirin derivatives from dihaloalkylene, such as. B. dibromobutane with bisdialkylamines, such as. B. bis-dimethylamino-1,3-propane, cationic guar gum, such as. B. Jaguar ® CBS, Jaguar ® C-17, Jaguar ® C-16 from Celanese, quaternized ammonium salt polymers, such as. B. Mirapol ® A-15, Mirapol ® AD-1, Mirapol ® AZ-1 from Miranol.
Als anionische, zwitterionische, amphotere und nichtionische Polymere kommen beispielsweise Vinylacetat/Crotonsäure-Copolymere, Vinylpyrrolidon/Vinylacrylat-Copolymere, Vinylacetat/Butylmaleat/ Iso-bornylacrylat-Copolymere, Methylvinylether/Maleinsäureanhydrid-Copolymere und deren Ester, unvernetzte und mit Polyolen vernetzte Polyacrylsäuren, Acrylamidopropyltrimethylammoniumchloridl Acrylat-Copolymere, Octylacrylamid/Methylmeth-acrylat/tert.Butylaminoethylmethacrylat/2-Hydroxypropyl-methacrylat-Copolymere, Polyvinylpyrrolidon, Vinylpyrrolidon/Vinylacetat-Copolymere, Vinylpyrrolidon/ Dimethylaminoethylmethacrylat/Vinylcaprolactam-Terpolymere sowie gegebenenfalls derivatisierte Celluloseether und Silicone in Frage.As anionic, zwitterionic, amphoteric and nonionic polymers come, for example, vinyl acetate / crotonic acid copolymers, Vinyl pyrrolidone / vinyl acrylate copolymers, vinyl acetate / butyl maleate / Isoboronyl acrylate copolymers, methyl vinyl ether / maleic anhydride copolymers and their esters, uncrosslinked and polyols crosslinked polyacrylic acids, acrylamidopropyltrimethylammonium chloride Acrylate copolymers, octylacrylamide / methyl methacrylate / tert-butylaminoethyl methacrylate / 2-hydroxypropyl methacrylate copolymers, polyvinylpyrrolidone, Vinyl pyrrolidone / vinyl acetate copolymers, vinyl pyrrolidone / dimethylaminoethyl methacrylate / vinyl caprolactam terpolymers and optionally derivatized cellulose ethers and silicones in question.
Siliconverbindungensilicone compounds
Neben den erfindungsgemäßen Verbindungen der Formel (I) können die erfindungsgemäßen Mittel noch weitere Silicium-haltigen Komponenten enthalten. Geeignete Siliconverbindungen sind beispielsweise Dimethylpolysiloxane, Methylphenylpolysiloxane, cyclische Silicone sowie amino-, fettsäure-, alkohol-, polyether-, epoxy-, fluor-, glykosid- und/oder alkyl-modifizierte Siliconverbindungen, die bei Raumtemperatur sowohl flüssig als auch harzförmig vorliegen können. Weiterhin geeignet sind Simethicone, bei denen es sich um Mischungen aus Dimethiconen mit einer durchschnittlichen Kettenlänge von 200 bis 300 Dimethylsiloxan-Einheiten und hydrierten Silicaten handelt.In addition to the compounds of the invention of formula (I) can the agents according to the invention still contain other silicon-containing components. Suitable silicone compounds are, for example, dimethylpolysiloxanes, methylphenylpolysiloxanes, cyclic silicones as well as amino, fatty acid, alcohol, polyether, epoxy-, fluorine-, glycoside- and / or alkyl-modified silicone compounds, which are both liquid at room temperature as well as resinous can be present. Simethicones, which are mixtures, are also suitable from dimethicones with an average chain length of 200 to 300 dimethylsiloxane units and hydrogenated silicates.
UV-Lichtschutzfilter und AntioxidantienUV light protection filter and antioxidants
Unter UV-Lichtschutzfaktoren sind beispielsweise bei Raumtemperatur flüssig oder kristallin vorliegende organische Substanzen (Lichtschutzfilter) zu verstehen, die in der Lage sind, ultraviolette Strahlen zu absorbieren und die aufgenommene Energie in Form längerwelliger Strahlung, z. B. Wärme wieder abzugeben. UVB-Filter können öllöslich oder wasserlöslich sein. Als öllösliche Substanzen sind z. B. zu nennen:
- – 3-Benzylidencampher bzw. 3-Benzylidennorcampher und dessen Derivate, z. B. 3-(4-Methylbenzyliden)campher.
- – 4-Aminobenzoesäurederivate, vorzugsweise 4-(Dimethylamino)benzoesäure-2-ethyl-hexylester, 4-(Dimethylamino)benzoesäure-2-octylester und 4-(Dimethylamino)benzoe-säureamylester
- – Ester der Zimtsäure, vorzugsweise 4-Methoxyzimtsäure-2-ethylhexylester, 4-Methoxyzimtsäure-propylester, 4-Methoxyzimtsäureisoamylester 2-Cyano-3,3-phenylzimtsäure-2-ethylhexylester (Octocrylene)
- – Ester der Salicylsäure, vorzugsweise Salicylsäure-2-ethylhexylester, Salicylsäure-4-iso-propylbenzylester, Salicylsäurehomomenthylester
- – Derivate des Benzophenons, vorzugsweise 2-Hydroxy-4-methoxybenzophenon, 2-Hydroxy-4-methoxy-4'-methylbenzophenon, 2,2'-Dihydroxy-4-methoxybenzophenon
- – Ester der Benzalmalonsäure, vorzugsweise 4-Methoxybenzmalonsäuredi-2-ethylhexyl-ester
- – Triazinderivate, wie z. B. 2,4,6-Trianilino-(p-carbo-2'-ethyl-1'-hexyloxy)-1,3,5-triazin und Octyl- Triazon, oder Dioctyl Butamido Triazone (Uvasorb® HEB)
- – Propan-1,3-dione, wie z. B. 1-(4-tert.Butylphenyl)-3-(4'methoxyphenyl)propan-1,3-dion
- – Ketotricyclo(5.2.1.0)decan-Derivate.
- - 3-benzylidene camphor or 3-benzylidene norcampher and its derivatives, e.g. B. 3- (4-Methylbenzylidene) camphor.
- 4-aminobenzoic acid derivatives, preferably 2-ethyl-hexyl 4- (dimethylamino) benzoate, 2-octyl 4- (dimethylamino) benzoate and amyl 4- (dimethylamino) benzoate
- Esters of cinnamic acid, preferably 4-methoxycinnamic acid 2-ethylhexyl ester, 4-methoxycinnamic acid propyl ester, 4-methoxycinnamic acid isamyl ester 2-cyano-3,3-phenylcinnamic acid 2-ethylhexyl ester (octocrylene)
- - Esters of salicylic acid, preferably salicylic acid 2-ethylhexyl ester, salicylic acid 4-iso-propylbenzyl ester, salicylic acid homomethyl ester
- - Derivatives of benzophenone, preferably 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4'-methylbenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone
- - Esters of benzalmalonic acid, preferably 4-methoxybenzmalonic acid di-2-ethylhexyl ester
- - Triazine derivatives, such as. B. 2,4,6-trianilino- (p-carbo-2'-ethyl-1'-hexyloxy) -1,3,5-triazine and octyl-triazone, or dioctyl butamido triazone (Uvasorb ® HEB)
- Propane-1,3-diones, such as e.g. B. 1- (4-tert-Butylphenyl) -3- (4'methoxyphenyl) propane-1,3-dione
- - Ketotricyclo (5.2.1.0) decane derivatives.
Als wasserlösliche Substanzen kommen in Frage:
- – 2-Phenylbenzimidazol-5-sulfonsäure und deren Alkali-, Erdalkali-, Ammonium-, Alkylammonium-, Alkanolammonium- und Glucammoniumsalze
- – Sulfonsäurederivate von Benzophenonen, vorzugsweise 2-Hydroxy-4-methoxybenzo-phenon-5-sulfonsäure und ihre Salze
- – Sulfonsäurederivate des 3-Benzylidencamphers, wie z. B. 4-(2-Oxo-3-bornylidenmethyl) benzolsulfonsäure und 2-Methyl-5-(2-oxo-3-bornyliden)sulfonsäure und deren Salze.
- - 2-Phenylbenzimidazole-5-sulfonic acid and its alkali, alkaline earth, ammonium, alkylammonium, alkanolammonium and glucammonium salts
- - Sulfonic acid derivatives of benzophenones, preferably 2-hydroxy-4-methoxybenzo-phenone-5-sulfonic acid and its salts
- - Sulfonic acid derivatives of 3-benzylidene camphor, such as. B. 4- (2-oxo-3-bornylidene methyl) benzenesulfonic acid and 2-methyl-5- (2-oxo-3-bornylidene) sulfonic acid and their salts.
Als typische UV-A-Filter kommen insbesondere
Derivate des Benzoylmethans in Frage, wie beispielsweise 1-(4'-tert.Butylphenyl)-3-(4'-methoxyphenyl)propan-1,3-dion,
4-tert.-Butyl-4'-methoxy-dibenzoylmethan (Parsol® 1789),
1-Phenyl-3-(4'-isopropylphenyl)-propan-1,3-dion
sowie Enaminverbindungen, wie beschrieben in der
Neben den genannten löslichen Stoffen kommen für diesen Zweck auch unlösliche Lichtschutzpigmente, nämlich feindisperse Metalloxide bzw. Salze in Frage. Beispiele für geeignete Metalloxide sind insbesondere Zinkoxid und Titandioxid und daneben Oxide des Eisens, Zirkoniums, Siliciums, Mangans, Aluminiums und Cers sowie deren Gemische. Als Salze können Silicate (Talk), Bariumsulfat oder Zinkstearat eingesetzt werden. Die Oxide und Salze werden in Form der Pigmente für hautpflegende und hautschützende Emulsionen und dekorative Kosmetik verwendet. Die Partikel sollten dabei einen mittleren Durchmesser von weniger als 100 nm, vorzugsweise zwischen 5 und 50 nm und insbesondere zwischen 15 und 30 nm aufweisen. Sie können eine sphärische Form aufweisen, es können jedoch auch solche Partikel zum Einsatz kommen, die eine ellipsoide oder in sonstiger Weise von der sphärischen Gestalt abweichende Form besitzen. Die Pigmente können auch oberflächenbehandelt, d. h. hydrophilisiert oder hydrophobiert vorliegen. Typische Beispiele sind gecoatete Titandioxide, wie z. B. Titandioxid T 805 (Degussa) oder Eusolex® T2000 (Merck). Als hydrophobe Coatingmittel kommen dabei vor allem Silicone und dabei speziell Trialkoxyoctylsilane oder Simethicone in Frage. In Sonnenschutzmitteln werden bevorzugt sogenannte Mikro- oder Nanopigmente eingesetzt. Vorzugsweise wird mikronisiertes Zinkoxid verwendet.In addition to the soluble substances mentioned, insoluble light protection pigments, namely finely dispersed metal oxides or salts, are also suitable for this purpose. Examples of suitable metal oxides are, in particular, zinc oxide and titanium dioxide and, in addition, oxides of iron, zirconium, silicon, manganese, aluminum and cerium and mixtures thereof. Silicates (talc), barium sulfate or zinc stearate can be used as salts. The oxides and salts are used in the form of the pigments for skin-care and skin-protecting emulsions and decorative cosmetics. The particles should have an average diameter of less than 100 nm, preferably between 5 and 50 nm and in particular between 15 and 30 nm. They can have a spherical shape, but it is also possible to use particles which have an ellipsoidal shape or a shape which differs in some other way from the spherical shape. The pigments can also be surface-treated, ie hydrophilized or hydrophobicized. Typical examples are coated titanium dioxide, such as. B. Titanium dioxide T 805 (Degussa) or Eusolex ® T2000 (Merck). Silicones, and in particular trialkoxyoctylsilanes or simethicones, are particularly suitable as hydrophobic coating agents. So-called micro- or nanopigments are preferably used in sunscreens. Micronized zinc oxide is preferably used.
Neben den beiden vorgenannten Gruppen primärer Lichtschutzstoffe können auch sekundäre Lichtschutzmittel vom Typ der Antioxidantien eingesetzt werden, die die photochemische Reaktionskette unterbrechen, welche ausgelöst wird, wenn UV-Strahlung in die Haut eindringt. Typische Beispiele hierfür sind Aminosäuren (z. B. Glycin, Histidin, Tyrosin, Tryptophan) und deren Derivate, Imidazole (z. B. Urocaninsäure) und deren Derivate, Peptide wie D,L-Carnosin, D-Carnosin, L-Carnosin und deren Derivate (z. B. Anserin), Carotinoide, Carotine (z. B. α-Carotin, β-Carotin, Lycopin) und deren Derivate, Chlorogensäure und deren Derivate, Liponsäure und deren Derivate (z. B. Dihydroliponsäure), Aurothioglucose, Propylthiouracil und andere Thiole (z. B. Thioredoxin, Glutathion, Cystein, Cystin, Cystamin und deren Glycosyl-, N-Acetyl-, Methyl-, Ethyl-, Propyl-, Amyl-, Butyl- und Lauryl-, Palmitoyl-, Oleyl-, γ-Linoleyl-, Cholesteryl- und Glycerylester) sowie deren Salze, Dilaurylthiodipropionat, Distearylthiodipropionat, Thiodipropionsäure und deren Derivate (Ester, Ether, Peptide, Lipide, Nukleotide, Nukleoside und Salze) sowie Sulfoximinverbindungen (z. B. Buthioninsulfoximine, Homocysteinsulfoximin, Butioninsulfone, Penta-, Hexa-, Heptathioninsulfoximin) in sehr geringen verträglichen Dosierungen (z. B. pmol bis μmol/kg), ferner (Metall)-Chelatoren (z. B. α-Hydroxyfettsäuren, Palmitinsäure, Phytinsäure, Lactoferrin), α-Hydroxysäuren (z. B. Citronensäure, Milchsäure, Äpfelsäure), Huminsäure, Gallensäure, Gallenextrakte, Bilirubin, Biliverdin, EDTA, EGTA und deren Derivate, ungesättigte Fettsäuren und deren Derivate (z. B. γ-Linolensäure, Linolsäure, Ölsäure), Folsäure und deren Derivate, Ubichinon und Ubichinol und deren Derivate, Vitamin C und Derivate (z. B. Ascorbylpalmitat, Mg-Ascorbylphosphat, Ascorbylacetat), Tocopherole und Derivate (z. B. Vitamin-E-acetat), Vitamin A und Derivate (Vitamin-Apalmitat) sowie Koniferylbenzoat des Benzoeharzes, Rutinsäure und deren Derivate, α-Glycosylrutin, Ferulasäure, Furfurylidenglucitol, Carnosin, Butylhydroxytoluol, Butylhydroxyanisol, Nordihydroguajakharzsäure, Nordihydroguajaretsäure, Trihydroxybutyrophenon, Harnsäure und deren Derivate, Mannose und deren Derivate, Superoxid-Dismutase, Zink und dessen Derivate (z. B. ZnO, ZnSO4) Selen und dessen Derivate (z. B. Selen-Methionin), Stilbene und deren Derivate (z. B. Stilbenoxid, trans-Stilbenoxid) und die erfindungsgemäß geeigneten Derivate (Salze, Ester, Ether, Zucker, Nukleotide, Nukleoside, Peptide und Lipide) dieser genannten Wirkstoffe.In addition to the two aforementioned groups of primary light stabilizers, it is also possible to use secondary light stabilizers of the antioxidant type which interrupt the photochemical reaction chain which is triggered when UV radiation penetrates the skin. Typical examples are amino acids (e.g. glycine, histidine, tyrosine, tryptophan) and their derivatives, imidazoles (e.g. urocanic acid) and their derivatives, peptides such as D, L-carnosine, D-carnosine, L-carnosine and their derivatives (e.g. anserine), carotenoids, carotenes (e.g. α-carotene, β-carotene, lycopene) and their derivatives, chlorogenic acid and its derivatives, lipoic acid and its derivatives (e.g. dihydroliponic acid), aurothioglucose , Propylthiouracil and other thiols (e.g. thioredoxin, glutathione, cysteine, cystine, cystamine and their glycosyl, N-acetyl, methyl, ethyl, propyl, amyl, butyl and lauryl, palmitoyl, Oleyl, γ-linoleyl, cholesteryl and glyceryl esters) and their salts, dilauryl thiodipropionate, distearyl thiodipropionate, thiodipropionic acid and their derivatives (esters, ethers, peptides, lipids, nucleotides, nucleosides and salts) as well as sulfoximine compounds (e.g. buthionocinsulfoximines, , Butioninsulfone, Penta-, Hexa-, Heptathioninsulfoximin) in very low tolerable doses (e.g. B. pmol to μmol / kg), further (metal) chelators (e.g. α-hydroxy fatty acids, palmitic acid, phytic acid, lactoferrin), α-hydroxy acids (e.g. citric acid, lactic acid, malic acid), humic acid, bile acid, Bile extracts, bilirubin, biliverdin, EDTA, EGTA and their derivatives, unsaturated fatty acids and their derivatives (e.g. γ-linolenic acid, linoleic acid, oleic acid), folic acid and their derivatives, ubiquinone and ubiquinol and their derivatives, vitamin C and derivatives (e.g. B. ascorbyl palmitate, Mg ascorbyl phosphate, ascorbyl acetate), tocopherols and derivatives (e.g. vitamin E acetate), vitamin A and derivatives (vitamin apalmitate) and coniferyl benzoate of benzoin, rutinic acid and its derivatives, α-glycosyl rutin, Ferulic acid, furfurylidene glucitol, carnosine, butylated hydroxytoluene, butylated hydroxyanisole, nordihydroguajakarzarzäure, nordihydroguajaretic acid, trihydroxybutyrophenone, uric acid and its derivatives, mannose and its derivatives, superoxide dismutase, zinc and its derivatives ( e.g. ZnO, ZnSO 4 ) selenium and its derivatives (e.g. B. selenium methionine), stilbenes and their derivatives (z. B. stilbene oxide, trans-stilbene oxide) and the derivatives suitable according to the invention (salts, esters, ethers, sugars, nucleotides, nucleosides, peptides and lipids) of these active ingredients.
Biogene WirkstoffeBiogenic agents
Unter biogenen Wirkstoffen sind beispielsweise Tocopherol, Tocopherolacetat, Tocopherolpalmitat, Ascorbinsäure, (Desoxy)Ribonucleinsäure und deren Fragmentierungsprodukte, β-Glucane, Retinol, Bisabolol, Allantoin, Phytantriol, Panthenol, AHA-Säuren, Aminosäuren, Ceramide, Pseudoceramide, essentielle Öle, Pflanzenextrakte, wie z. B. Prunusextrakt, Bambaranussextrakt und Vitaminkomplexe zu verstehen.Biogenic active ingredients are, for example Tocopherol, tocopherol acetate, tocopherol palmitate, ascorbic acid, (deoxy) ribonucleic acid and their fragmentation products, β-glucans, Retinol, bisabolol, allantoin, phytantriol, panthenol, AHA acids, amino acids, ceramides, Pseudoceramides, essential oils, plant extracts, such as B. Prunus extract, Bambaranus extract and vitamin complexes to understand.
Deodorantien und keimhemmende MittelDeodorants and germ-inhibiting medium
Kosmetische Deodorantien (Desodorantien) wirken Körpergerüchen entgegen, überdecken oder beseitigen sie. Körpergerüche entstehen durch die Einwirkung von Hautbakterien auf apokrinen Schweiß, wobei unangenehm riechende Abbauprodukte gebildet werden. Dementsprechend enthalten Deodorantien Wirkstoffe, die als keimhemmende Mittel, Enzyminhibitoren, Geruchsabsorber oder Geruchsüberdecker fungieren.Cosmetic deodorants (deodorants) counteract body odors, mask them or eliminate them. Body odors arise by the action of skin bacteria on apocrine sweat, being uncomfortable smelling degradation products are formed. Accordingly included Deodorants Active ingredients that act as germ inhibitors, enzyme inhibitors, Odor absorber or odor masker act.
Keimhemmende MittelAnti-germ agents
Als keimhemmende Mittel sind grundsätzlich alle gegen grampositive Bakterien wirksamen Stoffe geeignet, wie z. B. 4-Hydroxybenzoesäure und ihre Salze und Ester, N-(4-Chlorphenyl)-N'-(3,4- dichlorphenyl)harnstoff, 2,4,4'-Trichlor-2''-hydroxy-diphenylether (Triclosan), 4-Chlor-3,5-dimethylphenol, 2,2''-Methylen-bis(6-brom-4-chlorphenol), 3-Methyl-4-(1-methylethyl)-phenol, 2-Benzyl-4-chlorphenol, 3-(4-Chlorphenoxy)-1,2-propandiol, 3-1od-2-propinylbutylcarbamat, Chlorhexidin, 3,4,4'-Trichlorcarbanilid (TTC), antibakterielle Riechstoffe, Thymol, Thymianöl, Eugenol, Nelkenöl, Menthol, Minzöl, Farnesol, Phenoxyethanol, Glycerinmonocaprinat, Glycerinmonocaprylat, Glycerinmonolaurat (GML), Diglycerinmonocaprinat (DMC), Salicylsäure-N-alkylamide wie z. B. Salicylsäure-n-octylamid oder Salicylsäure-n-decylamid.In principle, all are germicidal agents substances effective against gram-positive bacteria, such as B. 4-hydroxybenzoic acid and their salts and esters, N- (4-chlorophenyl) -N '- (3,4-dichlorophenyl) urea, 2,4,4'-trichloro-2' '- hydroxy-diphenyl ether (triclosan), 4-chloro-3,5-dimethylphenol, 2,2 '' methylene bis (6-bromo-4-chlorophenol), 3-methyl-4- (1-methylethyl) phenol, 2-benzyl-4-chlorophenol, 3- (4-chlorophenoxy) -1,2-propanediol, 3-1od-2-propynyl butyl carbamate, chlorhexidine, 3,4,4'-trichlorocarbanilide (TTC), antibacterial fragrances, thymol, thyme oil, eugenol, Clove oil, Menthol, mint oil, Farnesol, phenoxyethanol, glycerol monocaprinate, glycerol monocaprylate, Glycerol monolaurate (GML), diglycerol monocaprinate (DMC), salicylic acid N-alkylamides such as B. Salicylic acid n-octylamide or salicylic acid-n-decylamide.
Enzyminhibitorenenzyme inhibitors
Als Enzyminhibitoren sind beispielsweise Esteraseinhibitoren geeignet. Hierbei handelt es sich vorzugsweise um Trialkylcitrate wie Trimethylcitrat, Tripropylcitrat, Triisopropylcitrat, Tributylcitrat und insbesondere Triethylcitrat (Hydagen® CAT). Die Stoffe inhibieren die Enzymaktivität und reduzieren dadurch die Geruchsbildung. Weitere Stoffe, die als Esteraseinhibitoren in Betracht kommen, sind Sterolsulfate oder -phosphate, wie beispielsweise Lanosterin-, Cholesterin-, Campesterin-, Stigmasterin- und Sitosterinsulfat bzw -phosphat, Dicarbonsäuren und deren Ester, wie beispielsweise Glutarsäure, Glutarsäuremonoethylester, Glutarsäurediethylester, Adipinsäure, Adipinsäuremonoethylester, Adipinsäurediethylester, Malonsäure und Malonsäurediethylester, Hydroxycarbonsäuren und deren Ester wie beispielsweise Citronensäure, Äpfelsäure, Weinsäure oder Weinsäurediethylester, sowie Zinkglycinat.Esterase inhibitors, for example, are suitable as enzyme inhibitors. These are preferably trialkyl citrates such as trimethyl citrate, tripropyl citrate, triisopropyl citrate, tributyl citrate and in particular triethyl citrate (Hydagen ® CAT). The substances inhibit enzyme activity and thereby reduce odor. Other substances which can be considered as esterase inhibitors are sterol sulfates or phosphates, such as, for example, lanosterol, cholesterol, campesteric, stigmasterol and sitosterol sulfate or phosphate, dicarboxylic acids and their esters, such as, for example, glutaric acid, glutaric acid monoethyl ester, glutaric acid diethyl ester, adipic acid, Monoethyl adipate, diethyl adipate, malonic acid and diethyl malonate, hydroxycarboxylic acids and their esters such as, for example, citric acid, malic acid, tartaric acid or tartaric acid diethyl ester, and zinc glycinate.
Geruchsabsorberodor absorbers
Als Geruchsabsorber eignen sich Stoffe, die geruchsbildende Verbindungen aufnehmen und weitgehend festhalten können. Sie senken den Partialdruck der einzelnen Komponenten und verringern so auch ihre Ausbreitungsgeschwindigkeit. Wichtig ist, dass dabei Parfums unbeeinträchtigt bleiben müssen. Geruchsabsorber haben keine Wirksamkeit gegen Bakterien. Sie enthalten beispielsweise als Hauptbestandteil ein komplexes Zinksalz der Ricinolsäure oder spezielle, weitgehend geruchsneutrale Duftstoffe, die dem Fachmann als "Fixateure" bekannt sind, wie z. B. Extrakte von Labdanum bzw. Styrax oder bestimmte Abietinsäurederivate. Als Geruchsüberdecker fungieren Riechstoffe oder Parfümöle, die zusätzlich zu ihrer Funktion als Geruchsüberdecker den Deodorantien ihre jeweilige Duftnote verleihen. Als Parfümöle seien beispielsweise genannt Gemische aus natürlichen und synthetischen Riechstoffen. Natürliche Riechstoffe sind Extrakte von Blüten, Stengeln und Blättern, Früchten, Fruchtschalen, Wurzeln, Hölzern, Kräutern und Gräsern, Nadeln und Zweigen sowie Harzen und Balsamen. Weiterhin kommen tierische Rohstoffe in Frage, wie beispielsweise Zibet und Castoreum. Typische synthetische Riechstoffverbindungen sind Produkte vom Typ der Ester, Ether, Aldehyde, Ketone, Alkohole und Kohlenwasserstoffe. Riechstoffverbindungen vom Typ der Ester sind z. B. Benzylacetat, p-tert.-Butylcyclohexylacetat, Linalylacetat, Phenylethylacetat, Linalylbenzoat, Benzylformiat, Allylcyclohexylpropionat, Styrallylpropionat und Benzylsalicylat. Zu den Ethern zählen beispielsweise Benzylethylether, zu den Aldehyden z. B. die linearen Alkanale mit 8 bis 18 Kohlenstoffatomen, Citral, Citronellol, Citronellyloxyacetaldehyd, Cyclamenaldehyd, Hydroxycitronellal, Lilial und Bourgeonal, zu den Ketonen z. B. die Jonone und Methylcedrylketon, zu den Alkoholen Anethol, Citronellol, Eugenol, Isoeugenol, Geraniol, Linalool, Phenylethylalkohol und Terpineol, zu den Kohlenwasserstoffen gehören hauptsächlich die Terpene und Balsame. Bevorzugt werden jedoch Mischungen verschiedener Riechstoffe verwendet, die gemeinsam eine ansprechende Duftnote erzeugen. Auch ätherische Öle geringerer Flüchtigkeit, die meist als Aromakomponenten verwendet werden, eignen sich als Parfümöle, z. B. Salbeiöl, Kamillenöl, Nelkenöl, Melissenöl, Minzenöl, Zimtblätteröl, Lindenblütenöl, Wacholderbeerenöl, Vetiveröl, Olibanöl, Galbanumöl, Labdanumöl und Lavandinöl. Vorzugsweise werden Bergamotteöl, Dihydromyrcenol, Lilial, Lyral, Citronellol, Phenylethylalkohol, α-Hexylzimtaldehyd, Geraniol, Benzylaceton, Cyclamenaldehyd, Linalool, Boisambrene Forte, Ambroxan, Indol, Hedione, Sandelice, Citronenöl, Mandarinenöl, Orangenöl, Allylamylglycolat, Cycloverfal, Lavandinöl, Muskateller Salbeiöl, β-Damascone, Geraniumöl Bourbon, Cyclohexylsalicylat, Vertofix Coeur, Fixolide NP, Evernyl, Iraldein gamma, Phenylessigsäure, Geranylacetat, Benzylacetat, Rosenoxid, Romilat, Irotyl und Floramat allein oder in Mischungen, eingesetzt.Suitable odor absorbers are substances absorb the odor-forming compounds and hold them to a large extent can. They lower and reduce the partial pressure of the individual components so also their speed of propagation. It is important that Perfumes unaffected have to stay. Odor absorbers are not effective against bacteria. They contain for example, the main ingredient is a complex zinc salt of ricinoleic acid or special, largely odorless fragrances, which are known to the person skilled in the art as "fixators", such as z. B. extracts of Labdanum or Styrax or certain abietic acid derivatives. As a smell masker act fragrances or perfume oils that additionally on their function as odor maskers give the deodorants their respective fragrance. As perfume oils are for example called mixtures of natural and synthetic fragrances. natural Fragrances are extracts from flowers, Stems and leaves, fruits, Fruit peel, roots, wood, herbs and grasses, Needles and twigs as well as resins and balms. Furthermore come animal Raw materials in question, such as civet and castoreum. typical synthetic fragrance compounds are products of the ester type, Ethers, aldehydes, ketones, alcohols and hydrocarbons. fragrance compounds of the ester type are e.g. B. benzyl acetate, p-tert-butylcyclohexyl acetate, Linalyl acetate, phenylethyl acetate, linalyl benzoate, benzyl formate, allyl cyclohexyl propionate, Styrallyl propionate and benzyl salicylate. The ethers include, for example Benzyl ethyl ether, to the aldehydes z. B. the linear alkanals 8 to 18 carbon atoms, citral, citronellol, citronellyloxyacetaldehyde, Cyclamenaldehyde, Hydroxycitronellal, Lilial and Bourgeonal, among the Ketones e.g. B. the Jonone and methylcedryl ketone, to the alcohols Anethole, citronellol, eugenol, isoeugenol, geraniol, linalool, phenylethyl alcohol and terpineol, the hydrocarbons mainly include the terpenes and balms. However, mixtures of different fragrances are preferably used, which together create an appealing fragrance. Also essential oils less Volatility, which are mostly used as aroma components are suitable as Perfume oils, e.g. B. Sage oil, Chamomile oil, Clove oil, Balm oil, Mint oil, Cinnamon leaf oil, linden blossom oil, juniper berry oil, vetiver oil, oliban oil, galbanum oil, labdanum oil and lavandin oil. Preferably become bergamot oil, Dihydromyrcenol, lilial, lyral, citronellol, phenylethyl alcohol, α-hexyl cinnamaldehyde, Geraniol, benzylacetone, cyclamenaldehyde, linalool, boisambrene forte, Ambroxan, indole, Hedione, Sandelice, lemon oil, mandarin oil, orange oil, allylamyl glycolate, Cycloverfal, lavandin oil, Muscatel sage oil, β-damascone, geranium Bourbon, cyclohexyl salicylate, Vertofix Coeur, Fixolide NP, Evernyl, Iraldein gamma, phenylacetic acid, Geranyl acetate, benzyl acetate, rose oxide, romilat, irotyl and floramat used alone or in mixtures.
Antitranspirantienantiperspirants
Antitranspirantien (Antiperspirantien) reduzieren durch Beeinflussung der Aktivität der ekkrinen Schweißdrüsen die Schweißbildung, und wirken somit Achselnässe und Körpergeruch entgegen. Wässrige oder wasserfreie Formulierungen von Antitranspirantien enthalten typischerweise folgende Inhaltsstoffe:
- – adstringierende Wirkstoffe
- – Ölkomponenten
- – nichtionische Emulgatoren
- – Coemulgatoren
- – Konsistenzgeber
- – Hilfsstoffe wie z. B. Verdicker oder Komplexierungsmittel und/oder
- – nichtwässrige Lösungsmittel wie z. B. Ethanol, Propylenglykol und/oder Glycerin.
- - astringent active ingredients
- - oil components
- - nonionic emulsifiers
- - co-emulsifiers
- - consistency generator
- - auxiliaries such as B. thickeners or complexing agents and / or
- - non-aqueous solvents such as As ethanol, propylene glycol and / or glycerin.
Als adstringierende Antitranspirant-Wirkstoffe eignen sich vor allem Salze des Aluminiums, Zirkoniums oder des Zinks. Solche geeigneten antihydrotisch wirksamen Wirkstoffe sind z. B. Aluminiumchlorid, Aluminiumchlorhydrat, Aluminiumdichlorhydrat, Aluminiumsesquichlorhydrat und deren Komplexverbindungen z. B. mit Propylenglycol-1,2. Aluminiumhydroxyallantoinat, Aluminiumchloridtartrat, Aluminium-Zirkonium-Trichlorohydrat, Aluminium-Zirkonium-tetrachlorohydrat, Aluminium-Zirkonium-pentachlorohydrat und deren Komplexverbindungen z. B. mit Aminosäuren wie Glycin. Daneben können in Antitranspirantien übliche öllösliche und wasserlösliche Hilfsmittel in geringeren Mengen enthalten sein.As an astringent antiperspirant active are particularly suitable salts of aluminum, zirconium or Zinc. Such suitable antiperspirant active ingredients are z. B. aluminum chloride, aluminum chlorohydrate, aluminum dichlorohydrate, Aluminum sesquichlorohydrate and their complex compounds e.g. B. with 1,2-propylene glycol. Aluminum hydroxyallantoinate, aluminum chloride tartrate, Aluminum zirconium trichlorohydrate, aluminum zirconium tetrachlorohydrate, Aluminum zirconium pentachlorohydrate and their complex compounds z. B. with amino acids like glycine. Next to it Oil-soluble and water-soluble auxiliaries customary in antiperspirants be contained in smaller quantities.
Solche öllöslichen Hilfsmittel können z. B. sein:
- – entzündungshemmende, hautschützende oder wohlriechende ätherische Öle
- – synthetische hautschützende Wirkstoffe und/oder
- – öllösliche Parfümöle.
- - anti-inflammatory, skin-protecting or fragrant essential oils
- - synthetic skin-protecting agents and / or
- - oil-soluble perfume oils.
Übliche wasserlösliche Zusätze sind z. B. Konservierungsmittel, wasserlösliche Duftstoffe, pH-Wert-Stellmittel, z. B. Puffergemische, wasserlösliche Verdickungsmittel, z. B. wasserlösliche natürliche oder synthetische Polymere wie z. B. Xanthan-Gum, Hydroxyethylcellulose, Polyvinylpyrrolidon oder hochmolekulare Polyethylenoxide.usual water-soluble additions are z. B. preservatives, water-soluble fragrances, pH adjusting agents, e.g. B. Buffer mixtures, water soluble Thickeners, e.g. B. water soluble natural or synthetic polymers such as B. xanthan gum, hydroxyethyl cellulose, Polyvinyl pyrrolidone or high molecular weight polyethylene oxides.
Filmbildnerfilm formers
Gebräuchliche Filmbildner sind beispielsweise Chitosan, mikrokristallines Chitosan, quaterniertes Chitosan, Polyvinylpyrrolidon, Vinylpyrrolidon-Vinylacetat-Copolymerisate, Polymere der Acrylsäurereihe, quaternäre Cellulose-Derivate, Kollagen, Hyaluronsäure bzw. deren Salze und ähnliche Verbindungen.Common film formers are, for example Chitosan, microcrystalline chitosan, quaternized chitosan, polyvinylpyrrolidone, Vinylpyrrolidone-vinyl acetate copolymers, polymers of the acrylic acid series, quaternary Cellulose derivatives, collagen, hyaluronic acid or its salts and the like Links.
AntischuppenwirkstoffeAntidandruff agents
Als Antischuppenwirkstoffe kommen Pirocton Olamin (1-Hydroxy-4-methyl-6-(2,4,4-trimythylpentyl)-2-(1 H)-pyridinonmonoethanolaminsalz), Baypival® (Climbazole), Ketoconazol®, (4-Acetyl-1-{-4-[2-(2.4-dichlorphenyl) r-2-(1N-imidazol-1-ylmethyl)-1,3-dioxylan-c-4-ylmethoxyphenyl}piperazin, Ketoconazol, Elubiol, Selendisulfid, Schwefel kolloidal, Schwefelpolyehtylenglykolsorbitanmonooleat, Schwefelrizinolpolyehtoxylat, Schwfel-teer Destillate, Salicylsäure (bzw. in Kombination mit Hexachlorophen), Undexylensäure Monoethanolamid Sulfosuccinat Na-Salz, Lamepon® UD (Protein-Undecylensäurekondensat), Zinkpyrithion, Aluminiumpyrithion und Magnesiumpyrithion / Dipyrithion-Magnesiumsulfat in Frage.Piroctone olamine (1-hydroxy-4-methyl-6- (2,4,4-trimythylpentyl) -2- (1 H) -pyridinone monoethanolamine salt), Baypival ® (climbazole), Ketoconazole ® , (4-acetyl- 1 - {- 4- [2- (2.4-dichlorophenyl) r-2- (1N-imidazol-1-ylmethyl) -1,3-dioxylan-c-4-ylmethoxyphenyl} piperazine, ketoconazole, elubiol, selenium disulfide, sulfur colloidal , Schwefelpolyehtylenglykolsorbitanmonooleat, Schwefelrizinolpolyehtoxylat, Schwfel tar distillate, salicylic acid (or in combination with hexachlorophene), undecylenic acid monoethanolamide sulfosuccinate Na salt, Lamepon UD ® (protein undecylenic acid condensate), zinc pyrithione, magnesium pyrithione Aluminiumpyrithion and / dipyrithione magnesium sulfate.
Quellmittelswelling agent
Als Quellmittel für wässrige Phasen können Montmorillonite, Clay Mineralstoffe, Pemulen sowie alkylmodifizierte Carbopoltypen (Goodrich) dienen.Montmorillonites, as swelling agents for aqueous phases, Clay minerals, pemules and alkyl-modified carbopol types (Goodrich) serve.
Insekten-RepellentienInsect repellents
Als Insekten-Repellentien kommen beispielsweise N,N-Diethyl-m-toluamid, 1,2-Pentandiol oder 3-(N-n-Butyl-N-acetyl-amino)-propionic acid-ethyl ester), welches unter der Bezeichnung Insect Repellent® 3535 von der Merck KGaA vertrieben wird, sowie Butylacetylaminopropionate in Frage.Suitable insect repellents are, for example, include N, N-diethyl-m-toluamide, 1,2-pentanediol or ethyl 3- (Nn-butyl-N-acetyl-amino) -propionic acid-ethyl ester), which under the name ® Insect Repellent 3535 is marketed by Merck KGaA, as well as butylacetylaminopropionate.
Selbstbräuner und DepigmentierungsmittelSelf tanner and depigmentation
Als Selbstbräuner eignet sich Dihydroxyaceton. Als Tyrosinhinbitoren, die die Bildung von Melanin verhindern und Anwendung in Depigmentierungsmitteln finden, kommen beispielsweise Arbutin, Ferulasäure, Kojisäure, Cumarinsäure und Ascorbinsäure (Vitamin C) in Frage.Dihydroxyacetone is suitable as a self-tanner. As tyrosine inhibitors that prevent the formation of melanin and Find application in depigmenting agents, for example Arbutin, ferulic acid, kojic acid, coumaric acid and ascorbic acid (Vitamin C) in question.
Hydrotropehydrotropes
Zur Verbesserung des Fließverhaltens können ferner Hydrotrope, wie beispielsweise Ethanol, Isopropylalkohol, oder Polyole eingesetzt werden. Polyole, die hier in Betracht kommen, besitzen vorzugsweise 2 bis 15 Kohlenstoffatome und mindestens zwei Hydroxylgruppen. Die Polyole können noch weitere funktionelle Gruppen, insbesondere Aminogruppen, enthalten bzw. mit Stickstoff modifiziert sein. Typische Beispiele sind:
- – Glycerin
- – Alkylenglycole, wie beispielsweise Ethylenglycol, Diethylenglycol, Propylenglycol, Butylenglycol, Hexylenglycol sowie Polyethylenglycole mit einem durchschnittlichen Molekulargewicht von 100 bis 1.000 Dalton
- – technische Oligoglyceringemische mit einem Eigenkondensationsgrad von 1,5 bis 10 wie etwa technische Diglyceringemische mit einem Diglyceringehalt von 40 bis 50 Gew.-%
- – Methyolverbindungen, wie insbesondere Trimethylolethan, Trimethylolpropan, Trimethylolbutan, Pentaerythrit und Dipentaerythrit
- – Niedrigalkylglucoside, insbesondere solche mit 1 bis 8 Kohlenstoffen im Alkylrest, wie beispielsweise Methyl- und Butylglucosid
- – Zuckeralkohole mit 5 bis 12 Kohlenstoffatomen, wie beispielsweise Sorbit oder Mannit
- – Zucker mit 5 bis 12 Kohlenstoffatomen, wie beispielsweise Glucose oder Saccharose
- – Aminozucker, wie beispielsweise Glucamin
- – Dialkoholamine, wie Diethanolamin oder 2-Amino-1,3-propandiol.
- - glycerin
- - Alkylene glycols, such as ethylene glycol, diethylene glycol, propylene glycol, butylene glycol, hexylene glycol and polyethylene glycols with an average molecular weight of 100 to 1,000 daltons
- Technical oligoglycerol mixtures with a degree of self-condensation of 1.5 to 10 such as technical diglycerol mixtures with a diglycerol content of 40 to 50% by weight
- - Methyl compounds, such as in particular trimethylolethane, trimethylolpropane, trimethylolbutane, pentaerythritol and dipentaerythritol
- - Lower alkyl glucosides, especially those with 1 to 8 carbons in the alkyl radical, such as methyl and butyl glucoside
- - Sugar alcohols with 5 to 12 carbon atoms, such as sorbitol or mannitol
- - Sugar with 5 to 12 carbon atoms, such as glucose or sucrose
- Aminosugars such as glucamine
- - Dialcohol amines, such as diethanolamine or 2-amino-1,3-propanediol.
Konservierungsmittelpreservative
Als Konservierungsmittel eignen sich beispielsweise Phenoxyethanol, Formaldehydlösung, Parabene, Pentandiol oder Sorbinsäure sowie die unter der Bezeichnung Surfacine® bekannten Silberkomplexe und die in Anlage 6, Teil A und B der Kosmetikverordnung aufgeführten weiteren Stoffklassen.Suitable preservatives are, for example, phenoxyethanol, formaldehyde solution, parabens, pentanediol or sorbic acid as well as the silver complexes known under the name Surfacine ® and the other classes of substances listed in Appendix 6, Parts A and B of the Cosmetics Regulation.
Parfümöle und AromenPerfume oils and flavors
Als Parfümöle seien genannt Gemische aus natürlichen und synthetischen Riechstoffen. Natürliche Riechstoffe sind Extrakte von Blüten (Lilie, Lavendel, Rosen, Jasmin, Neroli, Ylang-Ylang), Stengeln und Blättern (Geranium, Patchouli, Petitgrain), Früchten (Anis, Koriander, Kümmel, Wacholder), Fruchtschalen (Bergamotte, Zitrone, Orangen), Wurzeln (Macis, Angelica, Sellerie, Kardamon, Costus, Iris, Calmus), Hölzern (Pinien-, Sandel-, Guajak-, Zedern-, Rosenholz), Kräutern und Gräsern (Estragon, Lemongras, Salbei, Thymian), Nadeln und Zweigen (Fichte, Tanne, Kiefer, Latschen), Harzen und Balsamen (Galbanum, Elemi, Benzoe, Myrrhe, Olibanum, Opoponax). Weiterhin kommen tierische Rohstoffe in Frage, wie beispielsweise Zibet und Castoreum. Typische synthetische Riechstoffverbindungen sind Produkte vom Typ der Ester, Ether, Aldehyde, Ketone, Alkohole und Kohlenwasserstoffe. Riechstoffverbindungen vom Typ der Ester sind z. B. Benzylacetat, Phenoxyethylisobutyrat, p-tert.-Butylcyclohexylacetat, Linalylacetat, Dimethylbenzylcarbinylacetat, Phenylethylacetat, Linalylbenzoat, Benzylformiat, Ethylmethylphenylglycinat, Allylcyclohexylpropionat, Styrallylpropionat und Benzylsalicylat. Zu den Ethern zählen beispielsweise Benzylethylether, zu den Aldehyden z. B. die linearen Alkanale mit 8 bis 18 Kohlenstoffatomen, Citral, Citronellal, Citronellyloxyacetaldehyd, Cyclamenaldehyd, Hydroxycitronellal, Lilial und Bourgeonal, zu den Ketonen z. B. die Jonone, α-Isomethylionon und Methylcedrylketon, zu den Alkoholen Anethol, Citronellol, Eugenol, Isoeugenol, Geraniol, Linalool, Phenylethylalkohol und Terpineol, zu den Kohlenwasserstoffen gehören hauptsächlich die Terpene und Balsame. Bevorzugt werden jedoch Mischungen verschiedener Riechstoffe verwendet, die gemeinsam eine ansprechende Duftnote erzeugen. Auch ätherische Öle geringerer Flüchtigkeit, die meist als Aromakomponenten verwendet werden, eignen sich als Parfümöle, z. B. Salbeiöl, Kamillenöl, Nelkenöl, Melissenöl, Minzenöl, Zimtblätteröl, Lindenblütenöl, Wacholderbeerenöl, Vetiveröl, Olibanöl, Galbanumöl, Labolanumöl und Lavandinöl. Vorzugsweise werden Bergamotteöl, Dihydromyrcenol, Lilial, Lyral, Citronellol, Phenylethylalkohol, α-Hexylzimtaldehyd, Geraniol, Benzylaceton, Cyclamenaldehyd, Linalool, Boisambrene Forte, Ambroxan, Indol, Hedione, Sandelice, Citronenöl, Mandarinenöl, Orangenöl, Allylamylglycolat, Cyclovertal, Lavandinöl, Muskateller Salbeiöl, β-Damascone, Geraniumöl Bourbon, Cyclohexylsalicylat, Vertofix Coeur, Iso-E-Super, Fixolide NP, Evernyl, Iraldein gamma, Phenylessigsäure, Geranylacetat, Benzylacetat, Rosenoxid, Romilllat, Irotyl und Floramat allein oder in Mischungen, eingesetzt.Mixtures are mentioned as perfume oils natural and synthetic fragrances. Natural fragrances are extracts of flowers (Lily, lavender, roses, jasmine, neroli, ylang-ylang), stems and leaves (Geranium, patchouli, petitgrain), fruits (anise, coriander, caraway, juniper), Fruit peels (bergamot, lemon, oranges), roots (Macis, Angelica, Celery, cardamom, costus, iris, calmus), wood (pine, sandal, guaiac, Cedar, rosewood), herbs and grasses (Tarragon, lemongrass, sage, thyme), needles and twigs (spruce, Fir, pine, mountain pine), resins and balsams (Galbanum, Elemi, Benzoin, myrrh, olibanum, opoponax). Furthermore come animal Raw materials in question, such as civet and castoreum. typical synthetic fragrance compounds are products of the ester type, Ethers, aldehydes, ketones, alcohols and hydrocarbons. fragrance compounds of the ester type are e.g. B. benzyl acetate, phenoxyethyl isobutyrate, p-tert-butylcyclohexyl acetate, linalyl acetate, dimethylbenzylcarbinyl acetate, Phenylethyl acetate, linalyl benzoate, benzyl formate, ethyl methylphenylglycinate, Allyl cyclohexyl propionate, styrallyl propionate and benzyl salicylate. Count among the ethers for example benzyl ethyl ether, to the aldehydes z. B. the linear Alkanals with 8 to 18 carbon atoms, citral, citronellal, citronellyloxyacetaldehyde, Cyclamenaldehyde, Hydroxycitronellal, Lilial and Bourgeonal, among the Ketones e.g. B. the Jonone, α-isomethyl ionone and Methyl cedryl ketone, to the alcohols anethole, citronellol, eugenol, Isoeugenol, geraniol, linalool, phenylethyl alcohol and terpineol, belong to the hydrocarbons mainly the terpenes and balms. However, mixtures of different are preferred Fragrances used that together have an appealing fragrance produce. Also essential oils less Volatility, which are mostly used as aroma components are suitable as Perfume oils, e.g. B. Sage oil, Chamomile oil, Clove oil, Balm oil, Mint oil, Cinnamon leaf oil, linden blossom oil, juniper berry oil, vetiver oil, oliban oil, galbanum oil, labolanum oil and lavandin oil. Preferably become bergamot oil, Dihydromyrcenol, lilial, lyral, citronellol, phenylethyl alcohol, α-hexyl cinnamaldehyde, geraniol, Benzylacetone, Cyclamenaldehyde, Linalool, Boisambrene Forte, Ambroxan, Indole, hedione, sandelice, lemon oil, mandarin oil, orange oil, allylamyl glycolate, Cyclover Valley, Lavender Oil, Muscatel sage oil, β-damascone, geranium Bourbon, cyclohexyl salicylate, Vertofix Coeur, Iso-E-Super, Fixolide NP, Evernyl, Iraldein gamma, phenylacetic acid, geranyl acetate, benzyl acetate, Rose oxide, romilllat, irotyl and floramat alone or in mixtures, used.
Als Aromen kommen beispielsweise Pfefferminzöl, Krauseminzöl, Anisöl, Sternanisöl, Kümmelöl, Eukalyptusöl, Fenchelöl, Citronenöl, Wintergrünöl, Nelkenöl, Menthol und dergleichen in Frage.For example, come as flavors Peppermint oil, spearmint, anise oil, star anise, Caraway oil, eucalyptus oil, fennel oil, lemon oil, wintergreen oil, clove oil, menthol and the like in question.
Farbstoffedyes
Als Farbstoffe können die für kosmetische Zwecke geeigneten und zugelassenen Substanzen verwendet werden. Beispiele sind Kochenillerot A (C.I. 16255), Patentblau V (C.I.42051), Indigotin (C.I.73015), Chlorophyllin (C.I.75810), Chinolingelb (C.I.47005), Titandioxid (C.I.77891), Indanthrenblau RS (C.I. 69800) und Krapplack (C.I.58000). Als Lumineszenzfarbstoff kann auch Luminol enthalten sein. Diese Farbstoffe werden üblicherweise in Konzentrationen von 0,001 bis 0,1 Gew.-%, bezogen auf die gesamte Mischung, eingesetzt.The dyes which can be used are those which are suitable and approved for cosmetic purposes be det. Examples are culinary red A (CI 16255), patent blue V (CI42051), indigotine (CI73015), chlorophyllin (CI75810), quinoline yellow (CI47005), titanium dioxide (CI77891), indanthrene blue RS (CI 69800) and madder varnish (CI58000). Luminol may also be present as the luminescent dye. These dyes are usually used in concentrations of 0.001 to 0.1% by weight, based on the mixture as a whole.
Die Herstellung der kosmetischen Mittel kann auf allen dem Fachmann bekanten Wegen geschehen. Die erfindungsgemäße Verwendung der Emulgatorengemische führt vorzugsweise zu Mitteln mit einer PIT im Bereich von 10 bis 30 °C. Die verwendeten Emulgatoren sind vorzugsweise nicht-ionischer Natur.The production of the cosmetic Means can be done in all ways known to the expert. The use according to the invention of the emulsifier mixtures preferably for agents with a PIT in the range from 10 to 30 ° C. The used Emulsifiers are preferably non-ionic in nature.
Zur chemischen Beschaffenheit insbesondere nichtionischer Emulgatoren, die zur Temperaturgesteuerten Phaseninversion befähigt sind, beziehungsweise zur Beschaffenheit entsprechende nichtionische Komponenten enthaltender Emulgatorsysteme kann auf das Fachbuchwissen und das sonstige druckschriftliche einschlägige Material verwiesen werden. Vorzugsweise werden solche Emulgatoren eingesetzte deren HLB-Werte im Bereich von 1 bis 20, insbesondere 6 bis 20 und vorzugsweise 7 bis 18 liegen. Im nachfolgenden werden dementsprechend einige zusätzliche, erfindungsgemäß bevorzugte Bestimmungselemente für die Auswahl der Emulgatoren beziehungsweise Emulgatorsysteme gebracht.The chemical nature in particular nonionic emulsifiers for temperature controlled phase inversion capable are, or non-ionic corresponding to the nature Components containing emulsifier systems can be based on specialist book knowledge and the other relevant printed material is referenced. Such emulsifiers are preferably used whose HLB values in the range from 1 to 20, in particular 6 to 20 and preferably 7 to 18. The following are accordingly some additional preferred according to the invention Determinants for brought the selection of emulsifiers or emulsifier systems.
Zur Steuerung und Anpassung des erwünschten Bereiches zur Phaseninversionstemperatur (PIT) an die jeweils vorgegebene Abmischung des Mittel – insbesondere unter Berücksichtigung der Auswahl der Ölphase nach Art und Menge sowie der Beladung der wäßrigen Phase mit löslichen Komponenten – hat es sich als hilfreich erwiesen, mehrkomponentige Emulgatorsysteme einzusetzen. Dabei können Abmischungen bevorzugt sein, die wenigstens eine Emulgator-Hauptkomponente zusammen mit Co-Emulgatoren enthalten. In einer bevorzugten Ausführungsform sind dabei wiederum Emulgator-Hauptkomponenten vorgesehen, die zusammen mit der Eignung zur Temperatur-gesteuerten Phaseninversion vergleichsweise höhere Zahlenwerte des HLB-Bereiches aufweisen. Komponenten mit entsprechenden HLB-Werten des Bereiches von etwa 6 bis 20 und vorzugsweise von 7 bis 18, haben sich als geeignete nichtionische Emulgator-Hauptkomponenten erwiesen. Diese Hauptkomponenten werden bevorzugt gemeinsam mit stärker lipophilen Co-Emulgatoren eingesetzt, die – bezogen auf die jeweilige(n) Emulgator-Hauptkomponente(n) – ihrerseits niedrigere HLB-(number)Werte besitzen. Brauchbare Co-Emulgatoren liegen dementsprechend zunächst einmal in dem Zahlenbereich unterhalb des zuvor genannten Zahlenbereiches für die Emulgator-Hauptkomponente(n). Geeignete Co-Emulgatoren können auch in diesen Zahlenbereich mit ihrem HLB-Wert fallen, liegen dann aber in der Regel bei niedrigeren Werten als die in Abmischung vorliegenden Emulgator-Hauptkomponente(n) mit ihren jeweils individuellen Zahlenwerten.To control and adjust the desired Range to the phase inversion temperature (PIT) to the respectively given one Mixing the agent - in particular considering the selection of the oil phase according to the type and amount as well as the loading of the aqueous phase with soluble ones Components - has multi-component emulsifier systems have been found to be helpful use. You can Mixtures may be preferred, the at least one emulsifier main component together with co-emulsifiers contain. In a preferred embodiment, again Principal emulsifier components provided that together with the suitability for temperature-controlled Phase inversion comparatively higher numerical values in the HLB range exhibit. Components with corresponding HLB values for the area from about 6 to 20, and preferably from 7 to 18, have proven to be suitable main non-ionic emulsifier components. This Main components are preferred together with more lipophilic ones Co-emulsifiers used, which - related on the respective main emulsifier component (s) - in turn have lower HLB (number) values. Usable co-emulsifiers are accordingly initially once in the number range below the previously mentioned number range for the Principal emulsifier component (s). Suitable co-emulsifiers can also be used in this range fall with their HLB value, but are then usually lower Values as the main emulsifier component (s) in admixture with their individual numerical values.
Aus dem großen Bereich der nichtionischen
Emulgatoren lassen sich erfindungsgemäß besonders geeignete Emulgator-Hauptkomponenten
und/oder Co-Emulgatoren wenigstens einer der nachfolgenden Stoffklassen
zuordnen:
(Oligo)-Alkoxylate – insbesondere niedrig-Alkoxylate,
wobei hier entsprechenden Ethoxylaten und/oder Propoxylaten besondere
Bedeutung zukommt – von
lipophile Reste enthaltenden und zur Alkoxylierung befähigten Grundmolekülen natürlichen
und/oder synthetischen Ursprungs. Dabei bestimmt in bekannter Weise
die Länge
der Alkoxylatreste im Verhältnis
zu den im Molekül
vorliegenden lipophilen Resten das jeweils gegebene Mischungsverhältnis von
hydrophilem und hydrophobem Verhalten und die damit verbundene Zuordnung
der HLB-Werte. Alkoxylate der angegebenen Art sind bekanntlich als
solche – d.h.
mit endständiger
freier Hydroxylgruppe am Alkoxylatrest – nicht-ionische Emulgatoren,
die entsprechenden Verbindungen können aber auch Endgruppen-verschlossen
sein, beispielsweise durch Veresterung und/oder Veretherung.From the large range of nonionic emulsifiers, according to the invention particularly suitable main emulsifier components and / or co-emulsifiers can be assigned to at least one of the following classes of substances:
(Oligo) alkoxylates - in particular low alkoxylates, in which case corresponding ethoxylates and / or propoxylates are of particular importance - of base molecules containing lipophilic residues and capable of alkoxylation of natural and / or synthetic origin. In a known manner, the length of the alkoxylate residues in relation to the lipophilic residues present in the molecule determines the respective mixing ratio of hydrophilic and hydrophobic behavior and the associated assignment of the HLB values. As is known, alkoxylates of the stated type are non-ionic emulsifiers as such - ie with a free hydroxyl group on the alkoxylate residue, but the corresponding compounds can also be end group-sealed, for example by esterification and / or etherification.
Eine weitere wichtige Klasse nichtionischer Emulgatoren für die Zwecke der Erfindung sind Partialester und/oder Partialether mehrfunktioneller Alkohole mit insbesondere 2 bis 6 C-Atomen und 2 bis 6 OH- Gruppen und/oder deren Oligomere mit lipophile Reste enthaltenden Säuren und/oder Alkoholen. Geeignet sind dabei insbesondere auch Verbindungen dieser Art, die zusätzlich in ihre Molekülstruktur (Oligo-)Alkoxyreste und dabei insbesondere entsprechende Oligo-Ethoxyreste eingebunden enthalten. Die polyfunktionellen Alkohole mit 2 bis 6 OH-Gruppen im Grundmolekül beziehungsweise die sich davon ableitenden Oligomeren können insbesondere Diole und/oder Triole beziehungsweise deren Oligomerisierungsprodukte sein, wobei dem Glykol und dem Glycerin oder ihren Oligomeren besondere Bedeutung zukommen kann. Aber auch andere polyfunktionelle Alkohole der hier zusammenfassend genannten Art wie Trimethylolpropan, Pentaerythrit bis hin zu Glykosiden – beziehungsweise ihren jeweiligen Oligomeren – können Grundmoleküle für die Umsetzung mit lipophile Reste enthaltenden Säuren und/oder Alkoholen sein, die dann wichtige Emulgatorkomponenten im erfindungsgemäßen Sinne sind. Dem Bereich von Partialethern mehrfunktioneller Alkohole sind auch bekannte nichtionische Emulgatoren von der Art der Ethylenoxid/Propylenoxid/Butylenoxid-Blockpolymeren zuzuordnen.Another important class of non-ionic Emulsifiers for the purposes of the invention are partial esters and / or partial ethers polyfunctional alcohols with in particular 2 to 6 carbon atoms and 2 to 6 OH groups and / or their oligomers with acids containing lipophilic residues and / or Alcohols. Connections of these are particularly suitable Kind of additionally into their molecular structure (Oligo) alkoxy residues and, in particular, corresponding oligo ethoxy residues included included. The polyfunctional alcohols with 2 to 6 OH groups in the base molecule or the oligomers derived therefrom can in particular Diols and / or triols or their oligomerization products be special, the glycol and the glycerin or their oligomers Meaning can be. But also other polyfunctional alcohols of the type summarized here, such as trimethylolpropane, pentaerythritol up to glycosides - respectively their respective oligomers - can be basic molecules for the implementation with acids and / or alcohols containing lipophilic residues, the then important emulsifier components in the sense of the invention are. The area of partial ethers of polyfunctional alcohols also known nonionic emulsifiers of the type of ethylene oxide / propylene oxide / butylene oxide block polymers assigned.
Ein weiteres Beispiel für entsprechende Emulgatorkomponenten sind Alkyl(poly)glykoside langkettiger Alkohole sowie die bereits benannten Fettalkohole natürlichen und/oder synthetischen Ursprungs beziehungsweise Alkylolamide, Aminoxide und Lecithine. Die Mitverwendung heute handelsüblicher Alkyl(poly)glykosid-Verbindungen (APG-Verbindungen) als Emulgatorkomponenten im erfindungsgemäßen Sinn kann u.a. deswegen besonders interessant sein, weil es sich hier um eine Emulgatorklasse besonders ausgeprägter Ökoverträglichkeit handelt. Dabei ist es z.B. zur Steuerung der Phaseninversion in die erfindungsgemäß beschriebenen Temperaturbereiche auch möglich anteilsweise andere Emulgatorhauptkomponenten, z.B. Niotensidverbindungen mit stärker ausgeprägtem Phaseninversionsverhalten mit zu verwenden. In Betracht kommen z.B. die schon mehrfach erwähnten Oligo-Alkoxylat-Verbindungen, insbesondere entsprechende Verbindungen vom Typ der Oligo-Ethoxylatkomponenten. Möglich ist es allerdings auch diese Variation der verbesserten Steuerbarkeit des Phaseninversionsverhaltens durch eine entsprechende Oligo-Alkoxylierung der APG-Komponenten selber einzustellen. Durch geeignete Auswahl der APG-Komponenten nach Art und Menge als Hauptemulgator und Co-Emulgatoren, z.B. heute üblicher W/O-Invert-Emulgatoren, können aber auch hier ohne weitere Hilfsstoffe mit Emulgatorwirkung die erfindungsgemäßen Anforderungen erfüllt werden.Another example of corresponding emulsifier components are alkyl (poly) glycosides of long-chain alcohols and the already mentioned fatty alcohols of natural and / or synthetic origin or alkylolamides, amine oxides and lecithins. The use of commercially available alkyl (poly) glycoside compounds (APG compounds) as emulsifier components in the sense of the invention can be particularly interesting, inter alia, because this is an emulsifier class which is particularly pronounced Eco-compatibility. For example, to control the phase inversion into the temperature ranges described according to the invention, it is also possible to use other main emulsifier components, for example nonionic surfactant compounds with a more pronounced phase inversion behavior. For example, the oligo-alkoxylate compounds already mentioned several times, in particular corresponding compounds of the oligo-ethoxylate component type, are suitable. However, it is also possible to adjust this variation of the improved controllability of the phase inversion behavior by appropriate oligoalkoxylation of the APG components itself. By suitable selection of the APG components according to type and amount as main emulsifier and co-emulsifiers, for example W / O invert emulsifiers customary today, the requirements according to the invention can also be met here without further auxiliaries having an emulsifier effect.
Ohne Anspruch auf Vollständigkeit seien aus den hier aufgezählten Stoffklassen geeigneter Emulgatorkomponenten zusätzlich die folgenden Vertreter benannt: Die (Oligo)-Alkoxylate von lipophile Reste enthaltenden Grundmolekülen können sich insbesondere von ausgewählten Vertretern aus den nachfolgenden Klassen der lipophile Reste enthaltenden Grundmoleküle ableiten: Fettalkohole, Fettsäuren, Fettamine, Fettamine, Fettsäure- und/oder Fettalkoholester und/oder -ether, Alkanolamide, Alkylphenole und/oder deren Umsetzungsprodukte mit Formaldehyd sowie weitere Umsetzungsprodukte von lipophile Reste enthaltenden Trägermolekülen mit niederen Alkoxiden. Wie angegeben können die jeweiligen Umsetzungsprodukte auch wenigstens anteilsweise Endgruppenverschlossen sein. Beispiele für Partialester und/oder Partialether mehrfunktioneller Alkohole sind insbesondere die entsprechenden Partialester mit Fettsäuren, beispielsweise von der Art der Glycerinmono- und/oder -diester, Glykolmonoester, entsprechende Partialester oligomerisierter mehrfunktioneller Alkohole, Sorbitanpartialester und dergleichen sowie entsprechende Verbindungen mit Ethergruppierungen. Solche Partialester und/oder -ether können insbesondere auch Grundmoleküle für eine (Oligo)-Alkoxylierung sein.Without claim of completeness be from the ones listed here Substance classes of suitable emulsifier components additionally the following representatives named: The (oligo) alkoxylates of lipophilic residues containing basic molecules can different from selected ones Representatives from the following classes of lipophilic residues basic molecules derive: fatty alcohols, fatty acids, Fatty amines, fatty amines, fatty acid and / or fatty alcohol esters and / or ethers, alkanolamides, alkylphenols and / or their reaction products with formaldehyde and others Reaction products of carrier molecules containing lipophilic residues lower alkoxides. As indicated, the respective reaction products also be at least partially closed end groups. Examples for partial esters and / or partial ethers of polyfunctional alcohols are in particular the corresponding partial esters with fatty acids, for example from Type of glycerol monoesters and / or diesters, glycol monoesters, corresponding Partial esters of oligomerized polyfunctional alcohols, sorbitan partial esters and the like and corresponding compounds with ether groups. Such partial esters and / or ethers can, in particular, also base molecules for an (oligo) alkoxylation his.
Wie zuvor schon ausgeführt, ist ein wesentliches Bestimmungselement für die erfindungsgemäße Lehre, daß die Emulgatoren/Emulgatorsysteme in ihrer Einsatzmenge im kosmetischen Mittel auf den hier vorliegenden Anteil an Ölphase abgestimmt sind. Bevorzugte Emulgatormengen liegen dementsprechend in dem Bereich von gleichlgrößer 1 Gew.-%, vorzugsweise in dem Bereich von 5 bis 60 Gew.-% – bezogen jeweils auf die Ölphase.As stated earlier, is an essential determining element for the teaching according to the invention, that the Emulsifiers / emulsifier systems in their use amount in the cosmetic Means are matched to the proportion of oil phase present here. preferred Amounts of emulsifier are accordingly in the range of 1% by weight or more, preferably in the range from 5 to 60% by weight, based in each case on the oil phase.
Das daß das Mengenverhältnis von Emulgatorhaupt- zur Nebenkomponente liegt dabei vorzugsweise im Bereich von 10 : 1 bis 2 : 1. Als Ölphasen können die oben bezeichnete Verbindungen allein oder in beliebigen Abmischungen verwendet werden. Bevorzugt ist die Verwendung von Emulgatorengemischen, enthaltend ein hydriertes Rizinusöl, welches mit 7 Teilen Ethylenoxid umgesetzt wurde als Hauptkomponente und als Nebenkomponente ein Fettalkohol der mit 12 Teilen Ethylenoxid umgesetzt wurde.That the quantity ratio of The main emulsifier to the secondary component is preferably in Range from 10: 1 to 2: 1. The compounds described above can be used as oil phases used alone or in any mixes. Prefers is the use of emulsifier mixtures containing a hydrogenated Castor oil, which was reacted with 7 parts of ethylene oxide as the main component and as a minor component a fatty alcohol with 12 parts of ethylene oxide was implemented.
In einer weiteren Ausführungsform werden kosmetische Emulsion beansprucht, welche eine Öl- und eine Wasserphase enthalten, wobei als Emulgatoren Mischungen gemäß der obigen Beschreibung verwendet werden. Diese Emulsionen weisen eine Phaseninversion im Temperaturbereich von -5 °C bis 45 °C auf, vorzugsweise im Temperaturbereich von 10 bis 30 °C.In another embodiment cosmetic emulsion are claimed, which an oil and a Contain water phase, mixtures as emulsifiers according to the above Description can be used. These emulsions have a phase inversion in the temperature range of -5 ° C up to 45 ° C on, preferably in the temperature range of 10 to 30 ° C.
Beispiel 1example 1
Es wurde eine Emulsion mit den folgenden
Inhaltsstoffen (INCI) hergestellt: Emulgatormischung:
Beispiel 2Example 2
Emulgatormischung:
Ölphase:
Claims (12)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2002156507 DE10256507A1 (en) | 2002-12-04 | 2002-12-04 | Use of emulsifier mixtures for the production of cosmetic products |
| PCT/EP2003/013201 WO2004050044A2 (en) | 2002-12-04 | 2003-11-25 | Use of emulsifier mixtures for the production of cosmetic substances |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2002156507 DE10256507A1 (en) | 2002-12-04 | 2002-12-04 | Use of emulsifier mixtures for the production of cosmetic products |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE10256507A1 true DE10256507A1 (en) | 2004-06-24 |
Family
ID=32335932
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2002156507 Withdrawn DE10256507A1 (en) | 2002-12-04 | 2002-12-04 | Use of emulsifier mixtures for the production of cosmetic products |
Country Status (2)
| Country | Link |
|---|---|
| DE (1) | DE10256507A1 (en) |
| WO (1) | WO2004050044A2 (en) |
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|---|---|---|---|---|
| ES2670415T3 (en) * | 2006-10-13 | 2018-05-30 | Cognis Ip Management Gmbh | Metastable aqueous emulsions of oil in water |
Family Cites Families (1)
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|---|---|---|---|---|
| JP2002104951A (en) * | 2000-09-27 | 2002-04-10 | Cognis Japan Ltd | Humectant comprising dialkyl carbonate, cosmetic, detergent and bathing agent containing the humectant |
-
2002
- 2002-12-04 DE DE2002156507 patent/DE10256507A1/en not_active Withdrawn
-
2003
- 2003-11-25 WO PCT/EP2003/013201 patent/WO2004050044A2/en not_active Ceased
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| Publication number | Publication date |
|---|---|
| WO2004050044A3 (en) | 2005-01-13 |
| WO2004050044A2 (en) | 2004-06-17 |
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