DE1278671B - Antiseptisches Reinigungsmittel - Google Patents
Antiseptisches ReinigungsmittelInfo
- Publication number
- DE1278671B DE1278671B DEST25666A DEST025666A DE1278671B DE 1278671 B DE1278671 B DE 1278671B DE ST25666 A DEST25666 A DE ST25666A DE ST025666 A DEST025666 A DE ST025666A DE 1278671 B DE1278671 B DE 1278671B
- Authority
- DE
- Germany
- Prior art keywords
- atom
- cleaning agent
- dione
- oxygen
- active ingredient
- 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.)
- Pending
Links
- 230000002421 anti-septic effect Effects 0.000 title claims description 5
- 239000003599 detergent Substances 0.000 title description 5
- 239000002994 raw material Substances 0.000 claims description 10
- 239000012459 cleaning agent Substances 0.000 claims description 8
- 239000004480 active ingredient Substances 0.000 claims description 7
- 239000000344 soap Substances 0.000 claims description 7
- 238000005406 washing Methods 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 125000004434 sulfur atom Chemical group 0.000 claims description 6
- 239000000460 chlorine Substances 0.000 claims description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 3
- -1 amphoteric Chemical group 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 3
- UXTZUUVTGMDXNG-UHFFFAOYSA-N 1,2-benzoxazine-3,4-dione Chemical class C1=CC=C2C(=O)C(=O)NOC2=C1 UXTZUUVTGMDXNG-UHFFFAOYSA-N 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 230000000845 anti-microbial effect Effects 0.000 claims description 2
- 239000004599 antimicrobial Substances 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 239000000271 synthetic detergent Substances 0.000 claims 1
- 230000008018 melting Effects 0.000 description 10
- 238000002844 melting Methods 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- GHNLJDPNIAIWOQ-UHFFFAOYSA-N 2h-1$l^{6},2-benzothiazine 1,1-dioxide Chemical compound C1=CC=C2S(=O)(=O)NC=CC2=C1 GHNLJDPNIAIWOQ-UHFFFAOYSA-N 0.000 description 1
- AIPDYRUQGNTLLE-UHFFFAOYSA-N 3-phenyl-1,3-benzoxazine-2,4-dione Chemical class O=C1OC=2C=CC=CC=2C(=O)N1C1=CC=CC=C1 AIPDYRUQGNTLLE-UHFFFAOYSA-N 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 244000199866 Lactobacillus casei Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 241000293871 Salmonella enterica subsp. enterica serovar Typhi Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229920001938 Vegetable gum Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- WPDGFKWDLXLZQM-UHFFFAOYSA-N chloroethane formic acid Chemical compound C(=O)O.C(C)Cl WPDGFKWDLXLZQM-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical class [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/15—Six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/04—1,3-Oxazines; Hydrogenated 1,3-oxazines
- C07D265/12—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems
- C07D265/14—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D265/24—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring with hetero atoms directly attached in positions 2 and 4
- C07D265/26—Two oxygen atoms, e.g. isatoic anhydride
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D291/00—Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms
- C07D291/08—Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Paper (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US49489465A | 1965-10-11 | 1965-10-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1278671B true DE1278671B (de) | 1968-09-26 |
Family
ID=23966402
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEST25666A Pending DE1278671B (de) | 1965-10-11 | 1966-07-20 | Antiseptisches Reinigungsmittel |
Country Status (3)
| Country | Link |
|---|---|
| CH (1) | CH475008A (fr) |
| DE (1) | DE1278671B (fr) |
| GB (1) | GB1099865A (fr) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2202872A (en) * | 1987-02-13 | 1988-10-05 | Grace W R & Co | Pitch control aid and dye assistant |
| US5031245B1 (en) * | 1989-04-20 | 1996-09-10 | Smith & Nephew | Gloves their manufacture and use |
| US5261421A (en) * | 1988-04-23 | 1993-11-16 | Smith & Nephew Plc | Gloves, their manufacture and use |
| KR20090090406A (ko) | 2000-12-18 | 2009-08-25 | 가부시키가이샤 이야쿠 분지 셋케이 겐쿠쇼 | 염증성 사이토카인 생산 유리 억제제 |
| WO2003103656A1 (fr) | 2002-06-06 | 2003-12-18 | 株式会社医薬分子設計研究所 | Derives hydroxyaryle o-substitues |
| EA009701B1 (ru) | 2002-06-06 | 2008-02-28 | Инститьют Оф Медисинал Молекьюлар Дизайн. Инк. | Противоаллергические средства |
-
1966
- 1966-06-01 GB GB2437566A patent/GB1099865A/en not_active Expired
- 1966-07-20 DE DEST25666A patent/DE1278671B/de active Pending
- 1966-07-27 CH CH1084566A patent/CH475008A/fr not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| GB1099865A (en) | 1968-01-17 |
| CH475008A (fr) | 1969-07-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1278671B (de) | Antiseptisches Reinigungsmittel | |
| DE2700367A1 (de) | Antibakterielles seifenstueck | |
| DE1542739A1 (de) | Schaedlingsbekaempfungsmittel | |
| DE2157272C3 (de) | Verwendung von bis-(p-Chlorphenoxy)acetylharnstoff | |
| DE3783070T2 (de) | Phenylharnstoffe. | |
| DE2441474A1 (de) | Bakteriostatische mittel | |
| DE1125581B (de) | Herstellung einer bakteriziden fluessigen Seife | |
| DE1094737B (de) | Verfahren zur Herstellung von Aryl-isocyanid-dihalogeniden | |
| DE2140765C3 (de) | Neue 2-(4'-Chlorbenzyl)-phenole, Verfahren zu ihrer Herstellung und bakteriostatisches Mittel | |
| US3790615A (en) | O,n-diphenylthiocarbamic acid esters | |
| DE2142913A1 (de) | Neue Diazoverbindungen und Verfahren zu ihrer Herstellung | |
| DE2041732A1 (de) | Acylierte Arylhydrazino-2-imidazoline,Verfahren zu ihrer Herstellung und ihre Verwendung als Ektoparasitizide | |
| EP0485890A2 (fr) | Utilisation de 1-azolyl-propane 2,3-disulstitués comme inhibiteurs de la phase de croissance pathogène des cellules de levures dimorphes | |
| DE852391C (de) | Verfahren zur Herstellung von neuen Estern der Dithiocarbaminsaeure | |
| DE1171561B (de) | Mittel zur Bekaempfung von Mikroorganismen | |
| EP0066769B1 (fr) | Fungicides pour la protection de matériaux | |
| DE832146C (de) | Verfahren zur Stabilisierung von technischem Chloral | |
| CH513156A (de) | Verfahren zur Herstellung von Pyrrolinverbindungen | |
| DE2022494A1 (de) | Fungizide Mittel | |
| DE2317109A1 (de) | Thiazolpyrimidinderivate | |
| DE1768003C3 (de) | Verfahren zur Herstellung von neuartigen Chlorsulfenylphenylisocyaniddichloriden | |
| DE890048C (de) | Verfahren zur Herstellung eines organischen, Stickstoff, Schwefel und Sauerstoff enthaltenden Produktes | |
| DE10318366A1 (de) | Mikrobizide Mittel | |
| DE2263121C3 (de) | Alkyl-2,3,3-trijodallyläther, Verfahren zu ihrer Herstellung und ihre Verwendung in Arzneimitteln | |
| DE1954454C3 (de) | Substituierte Carbanilide |