DE10013763A1 - Verwendung von Duftalkoholalkoxylaten in Wasch- und Reinigungsmitteln und kosmetischen Zubereitungen - Google Patents

Verwendung von Duftalkoholalkoxylaten in Wasch- und Reinigungsmitteln und kosmetischen Zubereitungen

Info

Publication number: DE10013763A1
Authority: DE; Germany
Prior art keywords: hydrogen; radical; fragrance; alkyl radical; general formula
Prior art date: 2000-03-20
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.): Ceased

Application number

DE2000113763

Other languages

German (de)

English (en)

Inventor

Thomas Gassenmeier

Lars Zander

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Henkel AG and Co KGaA

Original Assignee

Henkel AG and Co KGaA

Priority date (The priority date 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 date listed.)

2000-03-20

Filing date

2000-03-20

Publication date

2001-10-18

2000-03-20 Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA

2000-03-20 Priority to DE2000113763 priority Critical patent/DE10013763A1/de

2001-03-17 Priority to AU42480/01A priority patent/AU4248001A/en

2001-03-17 Priority to EP01915371A priority patent/EP1265980A1/fr

2001-03-17 Priority to PCT/EP2001/003088 priority patent/WO2001070925A1/fr

2001-10-18 Publication of DE10013763A1 publication Critical patent/DE10013763A1/de

Status Ceased legal-status Critical Current

Links

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239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000000835 fiber Substances 0.000 description 1
230000009969 flowable effect Effects 0.000 description 1
238000005187 foaming Methods 0.000 description 1
239000004864 galbanum Substances 0.000 description 1
WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 1
229940113087 geraniol Drugs 0.000 description 1
229940091561 guaiac Drugs 0.000 description 1
239000000118 hair dye Substances 0.000 description 1
230000003694 hair properties Effects 0.000 description 1
239000008266 hair spray Substances 0.000 description 1
230000003741 hair volume Effects 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000008216 herbs Nutrition 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
WPFVBOQKRVRMJB-UHFFFAOYSA-N hydroxycitronellal Chemical compound O=CCC(C)CCCC(C)(C)O WPFVBOQKRVRMJB-UHFFFAOYSA-N 0.000 description 1
230000003752 improving hair Effects 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
229930002839 ionone Natural products 0.000 description 1
150000002499 ionone derivatives Chemical class 0.000 description 1
239000004922 lacquer Substances 0.000 description 1
239000001102 lavandula vera Substances 0.000 description 1
235000018219 lavender Nutrition 0.000 description 1
239000004571 lime Substances 0.000 description 1
229930007744 linalool Natural products 0.000 description 1
UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 1
239000000865 liniment Substances 0.000 description 1
150000002632 lipids Chemical class 0.000 description 1
239000006210 lotion Substances 0.000 description 1
239000001115 mace Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000005259 measurement Methods 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000001702 nutmeg Substances 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000009965 odorless effect Effects 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 1
235000011837 pasties Nutrition 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
229940067107 phenylethyl alcohol Drugs 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
230000008092 positive effect Effects 0.000 description 1
230000002265 prevention Effects 0.000 description 1
239000002994 raw material Substances 0.000 description 1
230000009467 reduction Effects 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
230000003381 solubilizing effect Effects 0.000 description 1
230000003068 static effect Effects 0.000 description 1
238000003860 storage Methods 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
229940116411 terpineol Drugs 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
239000001585 thymus vulgaris Substances 0.000 description 1
125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 0.000 description 1

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
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2068—Ethers
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Engineering & Computer Science (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Organic Chemistry (AREA)
Wood Science & Technology (AREA)
Chemical Kinetics & Catalysis (AREA)
Emergency Medicine (AREA)
Epidemiology (AREA)
Birds (AREA)
Cosmetics (AREA)
Detergent Compositions (AREA)

DE2000113763 2000-03-20 2000-03-20 Verwendung von Duftalkoholalkoxylaten in Wasch- und Reinigungsmitteln und kosmetischen Zubereitungen Ceased DE10013763A1 (de)

Priority Applications (4)

Application Number	Priority Date	Filing Date	Title
DE2000113763 DE10013763A1 (de)	2000-03-20	2000-03-20	Verwendung von Duftalkoholalkoxylaten in Wasch- und Reinigungsmitteln und kosmetischen Zubereitungen
AU42480/01A AU4248001A (en)	2000-03-20	2001-03-17	Use of aromatic alcohol alxoxylates in detergents and cosmetic formulations
EP01915371A EP1265980A1 (fr)	2000-03-20	2001-03-17	Utilisation d'alcoxylates d'alcool parfume dans des agents de lavage et de rin age et des preparations cosmetiques
PCT/EP2001/003088 WO2001070925A1 (fr)	2000-03-20	2001-03-17	Utilisation d'alcoxylates d'alcool parfume dans des agents de lavage et de rinçage et des preparations cosmetiques

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2000113763 DE10013763A1 (de)	2000-03-20	2000-03-20	Verwendung von Duftalkoholalkoxylaten in Wasch- und Reinigungsmitteln und kosmetischen Zubereitungen

Publications (1)

Publication Number	Publication Date
DE10013763A1 true DE10013763A1 (de)	2001-10-18

Family

ID=7635621

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE2000113763 Ceased DE10013763A1 (de)	2000-03-20	2000-03-20	Verwendung von Duftalkoholalkoxylaten in Wasch- und Reinigungsmitteln und kosmetischen Zubereitungen

Country Status (4)

Country	Link
EP (1)	EP1265980A1 (fr)
AU (1)	AU4248001A (fr)
DE (1)	DE10013763A1 (fr)
WO (1)	WO2001070925A1 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BR112014018842A2 (pt) *	2012-01-31	2018-09-11	Basf Se	alcoxilato de farnesol, processo para a preparação de um composto, uso de pelo menos um composto ou de um produto de reação, composição, e, método de lavagem, enxágue, limpeza ou acabamento
WO2013113831A1 (fr) *	2012-01-31	2013-08-08	Basf Se	Alcoxylates de farnésols le cas échéant hydrogénés et leur utilisation

Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CS253437B1 (sk) *	1986-04-11	1987-11-12	Milan Paulovic	Tenzid s nízkou penivosťou a příjemnou vdňon
WO1996001245A1 (fr) *	1994-07-01	1996-01-18	Rhone Poulenc Chimie	Derives terpeniques polyalcoxyles et compositions en contenant
DE19812245A1 (de) *	1998-03-20	1999-09-23	Clariant Gmbh	Neue Terpenether und deren Anwendungen

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1403903A (fr) *	1963-06-13	1965-06-25		Perfectionnements aux distributeurs de commande pour fluides sous pression
DE4124701A1 (de) *	1991-07-25	1993-01-28	Henkel Kgaa	Verfahren zur herstellung fester wasch- und reinigungsmittel mit hohem schuettgewicht und verbesserter loesegeschwindigkeit
FR2757508B1 (fr) *	1996-12-20	1999-02-26	Rhodia Chimie Sa	Composes terpeniques polyalcoxyles, leur procede de preparation et leur utilisation comme agents demoussants
JP2000026268A (ja) *	1998-07-10	2000-01-25	Kao Corp	皮膚外用剤
EP1268382A2 (fr) *	2000-03-20	2003-01-02	Henkel Kommanditgesellschaft auf Aktien	Alcools de substances odorantes alcoxyles et leur utilisation

2000
- 2000-03-20 DE DE2000113763 patent/DE10013763A1/de not_active Ceased
2001
- 2001-03-17 EP EP01915371A patent/EP1265980A1/fr not_active Withdrawn
- 2001-03-17 AU AU42480/01A patent/AU4248001A/en not_active Abandoned
- 2001-03-17 WO PCT/EP2001/003088 patent/WO2001070925A1/fr not_active Ceased

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CS253437B1 (sk) *	1986-04-11	1987-11-12	Milan Paulovic	Tenzid s nízkou penivosťou a příjemnou vdňon
WO1996001245A1 (fr) *	1994-07-01	1996-01-18	Rhone Poulenc Chimie	Derives terpeniques polyalcoxyles et compositions en contenant
DE19812245A1 (de) *	1998-03-20	1999-09-23	Clariant Gmbh	Neue Terpenether und deren Anwendungen

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Chem. Abstr. [online] Am. Chem. Soc. [recher. am 19.12.00] in STN, AN 1989:460019 CAPLUS *

Also Published As

Publication number	Publication date
WO2001070925A1 (fr)	2001-09-27
EP1265980A1 (fr)	2002-12-18
AU4248001A (en)	2001-10-03

Publication	Publication Date	Title
DE69933191T2 (de)	2007-08-23	Haarkosmetische Zusammensetzung
DE19646869C1 (de)	1997-12-04	Kosmetische Zubereitungen
EP1434556A1 (fr)	2004-07-07	Preparations cosmetiques et / ou pharmaceutiques
EP1434558A1 (fr)	2004-07-07	Preparations cosmetiques et/ou pharmaceutiques surgraissantes
EP1052972A1 (fr)	2000-11-22	Agents pour apres-shampooing
EP1434559B1 (fr)	2008-12-03	Preparations cosmetiques et/ou pharmaceutiques
DE19730649C1 (de)	1998-09-24	Detergensgemische
EP1265587A1 (fr)	2002-12-18	Colorants capillaires contenant des biopolymeres cationiques
DE19818410A1 (de)	1999-10-28	Haar- und Körperreinigungsmittel mit verminderter Hautirritation
DE19909552C1 (de)	2000-07-27	Haarwaschmittel
AT397342B (de)	1994-03-25	Haarkonditioniermittel
DE10013763A1 (de)	2001-10-18	Verwendung von Duftalkoholalkoxylaten in Wasch- und Reinigungsmitteln und kosmetischen Zubereitungen
WO2003032930A1 (fr)	2003-04-24	Shampooing conditionneur
EP1942178B1 (fr)	2010-03-17	Mélanges de 3-(4-Méthyl-cyclohex-3-ényl)-butyraldéhyde et 2,6-Diméthyl-7-octén-2-ol
DE10008307A1 (de)	2001-09-06	Nanokapseln
WO1998049998A2 (fr)	1998-11-12	Utilisation de composes de silicium glycosidiques pour la production de preparations cosmetiques et/ou pharmaceutiques
EP1268382A2 (fr)	2003-01-02	Alcools de substances odorantes alcoxyles et leur utilisation
WO2007042410A1 (fr)	2007-04-19	Preparation de nettoyage desodorisante
DE10013764A1 (de)	2001-10-11	Verwendung von Duftalkoholalkoxylaten in haarkosmetischen Mitteln
EP1390001A2 (fr)	2004-02-25	Produits de soins capillaires contenant des huiles naturelles
DE10013765A1 (de)	2001-10-18	Verwendung von Duftalkoholalkoxylaten als Solubilisierhilfsmittel
EP1021164B1 (fr)	2002-02-27	Produits de beaute
DE19727903C1 (de)	1998-07-30	Nicht-auszuspülendes Haarpflegemittel
DE10013762A1 (de)	2001-10-11	Alkoxylierte Duftalkohole, insbesondere Terpenalkohole, und ihre Verwendung in Wasch-, Spül- oder Reinigungsmitteln oder kosmetischen Zubereitungen
WO1989001770A1 (fr)	1989-03-09	Produit pulverisable de nettoyage du corps ou des cheveux, procede de nettoyage doux du corps ou des cheveux

Legal Events

Date	Code	Title	Description
2001-10-18	OP8	Request for examination as to paragraph 44 patent law
2005-01-13	8131	Rejection