NL8902942A - Alkyleenoxyde bevattende amfotere oppervlakteactieve middelen en preparaten die ze bevatten. - Google Patents

Alkyleenoxyde bevattende amfotere oppervlakteactieve middelen en preparaten die ze bevatten. Download PDF

Info

Publication number: NL8902942A
Authority: NL; Netherlands
Prior art keywords: formula; carbon atoms; mixture; compound; group
Prior art date: 1988-11-30

Application number

NL8902942A

Other languages

English (en)

Dutch (nl)

Original Assignee

Sandoz Ag

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.)

1988-11-30

Filing date

1989-11-29

Publication date

1990-06-18

1989-11-29 Application filed by Sandoz Ag filed Critical Sandoz Ag

1990-06-18 Publication of NL8902942A publication Critical patent/NL8902942A/nl

Links

238000002360 preparation method Methods 0.000 title claims description 21
239000004094 surface-active agent Substances 0.000 title claims description 19
150000001875 compounds Chemical class 0.000 claims description 73
239000000203 mixture Substances 0.000 claims description 58
125000004432 carbon atom Chemical group C* 0.000 claims description 35
125000000217 alkyl group Chemical group 0.000 claims description 27
239000002453 shampoo Substances 0.000 claims description 25
238000009472 formulation Methods 0.000 claims description 21
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 18
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 12
150000001768 cations Chemical class 0.000 claims description 9
229910052783 alkali metal Inorganic materials 0.000 claims description 8
150000001340 alkali metals Chemical class 0.000 claims description 7
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 6
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 5
150000001342 alkaline earth metals Chemical class 0.000 claims description 5
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 claims description 4
150000004820 halides Chemical class 0.000 claims description 4
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 3
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
150000001450 anions Chemical class 0.000 claims description 3
229910052700 potassium Inorganic materials 0.000 claims description 3
239000011591 potassium Substances 0.000 claims description 3
229910052708 sodium Inorganic materials 0.000 claims description 3
239000011734 sodium Substances 0.000 claims description 3
239000003945 anionic surfactant Substances 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims 3
239000001257 hydrogen Substances 0.000 claims 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
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238000006243 chemical reaction Methods 0.000 description 26
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XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
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125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
239000000543 intermediate Substances 0.000 description 7
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IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
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239000007864 aqueous solution Substances 0.000 description 4
GUPWNYUKYICHQX-UHFFFAOYSA-N carbonobromidic acid Chemical compound OC(Br)=O GUPWNYUKYICHQX-UHFFFAOYSA-N 0.000 description 4
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AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 3
235000008733 Citrus aurantifolia Nutrition 0.000 description 3
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235000011941 Tilia x europaea Nutrition 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
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239000011149 active material Substances 0.000 description 3
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125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 3
239000007795 chemical reaction product Substances 0.000 description 3
239000003599 detergent Substances 0.000 description 3
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JDJSXRYWPLNWOU-UHFFFAOYSA-N ethyl 2,2-diethoxy-2-tetradecoxyethaneperoxoate Chemical compound CCCCCCCCCCCCCCOC(OCC)(OCC)C(=O)OOCC JDJSXRYWPLNWOU-UHFFFAOYSA-N 0.000 description 3
239000006260 foam Substances 0.000 description 3
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FDRCDNZGSXJAFP-UHFFFAOYSA-M sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 description 3
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DRGCZXOFCUVKDS-UHFFFAOYSA-N CCCCCCCCCCCCN(C(C(OCC)(OCC)OCC)=O)OCC.Cl Chemical compound CCCCCCCCCCCCN(C(C(OCC)(OCC)OCC)=O)OCC.Cl DRGCZXOFCUVKDS-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
235000013162 Cocos nucifera Nutrition 0.000 description 2
244000060011 Cocos nucifera Species 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
206010022998 Irritability Diseases 0.000 description 2
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
125000002877 alkyl aryl group Chemical group 0.000 description 2
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239000011575 calcium Substances 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
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239000003795 chemical substances by application Substances 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
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125000001309 chloro group Chemical group Cl* 0.000 description 2
239000004205 dimethyl polysiloxane Substances 0.000 description 2
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229910052749 magnesium Inorganic materials 0.000 description 2
239000011777 magnesium Substances 0.000 description 2
LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
230000004048 modification Effects 0.000 description 2
238000012986 modification Methods 0.000 description 2
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QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
238000007086 side reaction Methods 0.000 description 2
239000012279 sodium borohydride Substances 0.000 description 2
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239000002904 solvent Substances 0.000 description 2
150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
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GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
150000000209 1-decanols Chemical class 0.000 description 1
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
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FDIPWBUDOCPIMH-UHFFFAOYSA-N 2-decylphenol Chemical compound CCCCCCCCCCC1=CC=CC=C1O FDIPWBUDOCPIMH-UHFFFAOYSA-N 0.000 description 1
CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 1
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125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
JOONSONEBWTBLT-UHFFFAOYSA-N 2-tetradecylphenol Chemical compound CCCCCCCCCCCCCCC1=CC=CC=C1O JOONSONEBWTBLT-UHFFFAOYSA-N 0.000 description 1
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AOMUHOFOVNGZAN-UHFFFAOYSA-N N,N-bis(2-hydroxyethyl)dodecanamide Chemical compound CCCCCCCCCCCC(=O)N(CCO)CCO AOMUHOFOVNGZAN-UHFFFAOYSA-N 0.000 description 1
QZXSMBBFBXPQHI-UHFFFAOYSA-N N-(dodecanoyl)ethanolamine Chemical group CCCCCCCCCCCC(=O)NCCO QZXSMBBFBXPQHI-UHFFFAOYSA-N 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
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150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
125000005210 alkyl ammonium group Chemical group 0.000 description 1
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239000008365 aqueous carrier Substances 0.000 description 1
229910052788 barium Inorganic materials 0.000 description 1
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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SOROIESOUPGGFO-UHFFFAOYSA-N diazolidinylurea Chemical compound OCNC(=O)N(CO)C1N(CO)C(=O)N(CO)C1=O SOROIESOUPGGFO-UHFFFAOYSA-N 0.000 description 1
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QKIUAMUSENSFQQ-UHFFFAOYSA-N dimethylazanide Chemical compound C[N-]C QKIUAMUSENSFQQ-UHFFFAOYSA-N 0.000 description 1
REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
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MDSQKJDNWUMBQQ-UHFFFAOYSA-M sodium myreth sulfate Chemical compound [Na+].CCCCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O MDSQKJDNWUMBQQ-UHFFFAOYSA-M 0.000 description 1
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238000005406 washing Methods 0.000 description 1
239000001993 wax Substances 0.000 description 1
PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
- A61K8/442—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C235/10—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by nitrogen atoms not being part of nitro or nitroso groups

Landscapes

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Public Health (AREA)
General Health & Medical Sciences (AREA)
Animal Behavior & Ethology (AREA)
Veterinary Medicine (AREA)
Epidemiology (AREA)
Birds (AREA)
Cosmetics (AREA)
Detergent Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

NL8902942A 1988-11-30 1989-11-29 Alkyleenoxyde bevattende amfotere oppervlakteactieve middelen en preparaten die ze bevatten. NL8902942A (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US27807088A	1988-11-30	1988-11-30
US27807088		1988-11-30

Publications (1)

Publication Number	Publication Date
NL8902942A true NL8902942A (nl)	1990-06-18

Family

ID=23063567

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8902942A NL8902942A (nl)	1988-11-30	1989-11-29	Alkyleenoxyde bevattende amfotere oppervlakteactieve middelen en preparaten die ze bevatten.

Country Status (8)

Country	Link
JP (1)	JPH02200615A (fr)
BE (1)	BE1003463A4 (fr)
CH (1)	CH678528A5 (fr)
DE (1)	DE3939315A1 (fr)
FR (1)	FR2639635B1 (fr)
GB (1)	GB2226557B (fr)
IT (1)	IT1238009B (fr)
NL (1)	NL8902942A (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5182033A (en) *	1991-06-14	1993-01-26	Sherex Chemical Company, Inc.	Polyamide salts
US5976520A (en) *	1996-11-12	1999-11-02	S. C. Johnson & Son, Inc.	Foamable skin preparations
DE19846537C2 (de) *	1998-10-09	2003-08-14	Cognis Deutschland Gmbh	Betaine
JP4562243B2 (ja) *	2000-05-26	2010-10-13	川研ファインケミカル株式会社	ポリオキシアルキレンアミドベタイン型界面活性化合物及びそれを含む界面活性剤

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NZ199856A (en) *	1981-03-09	1984-08-24	Johnson & Johnson Baby Prod	Non-zwitterionic amphoteric-fatty acid complexes and detergent compositions
DE3505269A1 (de) *	1985-02-15	1986-08-21	Hoechst Ag, 6230 Frankfurt	Quarternaere alkylamidobetainester, ein verfahren zu ihrer herstellung und ihre verwendung in waescheweichspuelmitteln
DE3613944C1 (de) *	1986-04-24	1987-08-13	Goldschmidt Ag Th	Verfahren zur Herstellung einer hochkonzentrierten,fliess- und pumpfaehigen Betainloesung
US4876034A (en) *	1986-11-18	1989-10-24	Kao Corporation	Secondary amidoamino acid based detergent composition

1989
- 1989-11-27 BE BE8901265A patent/BE1003463A4/fr not_active IP Right Cessation
- 1989-11-27 FR FR898915765A patent/FR2639635B1/fr not_active Expired - Lifetime
- 1989-11-27 GB GB8926786A patent/GB2226557B/en not_active Expired - Lifetime
- 1989-11-27 CH CH4235/89A patent/CH678528A5/de not_active IP Right Cessation
- 1989-11-28 DE DE3939315A patent/DE3939315A1/de not_active Withdrawn
- 1989-11-29 IT IT04861189A patent/IT1238009B/it active IP Right Grant
- 1989-11-29 NL NL8902942A patent/NL8902942A/nl not_active Application Discontinuation
- 1989-11-29 JP JP1307829A patent/JPH02200615A/ja active Pending

Also Published As

Publication number	Publication date
IT8948611A0 (it)	1989-11-29
CH678528A5 (fr)	1991-09-30
BE1003463A4 (fr)	1992-03-31
IT8948611A1 (it)	1991-05-29
DE3939315A1 (de)	1990-05-31
GB8926786D0 (en)	1990-01-17
JPH02200615A (ja)	1990-08-08
GB2226557A (en)	1990-07-04
FR2639635B1 (fr)	1992-06-12
IT1238009B (it)	1993-06-21
GB2226557B (en)	1992-05-06
FR2639635A1 (fr)	1990-06-01

Legal Events

Date	Code	Title	Description
1996-06-03	BV	The patent application has lapsed

Publication	Publication Date	Title
US4766153A (en)	1988-08-23	Alkyl polyoxyalkylene carboxylate esters and skin care compositions containing the same
EP0789619B1 (fr)	2003-01-22	Compositions d'emulsifiants a base d'esters de phosphates d'alcools gras
EP0522756B1 (fr)	1996-01-31	Terpolymères ampholyte avec des propriétés de conditionnement supérieur employer dans des shampooings et d'autres produits pour les soins des cheveux
JP2744099B2 (ja)	1998-04-28	シェービング組成物
JP3608844B2 (ja)	2005-01-12	高粘度液体洗浄剤組成物
US4087466A (en)	1978-05-02	Polycondensation of glycidol on alpha diols with fatty chain with alkaline catalysts, products thus obtained and utilization
JP3529391B2 (ja)	2004-05-24	ケラチン物質の洗浄組成物および洗浄方法
EP1074243A2 (fr)	2001-02-07	Compositions cosmétiques
JP3524223B2 (ja)	2004-05-10	ポリオキシプロピレン脂肪酸イソプロパノールアミド混合物を含有する増粘された洗浄剤組成物
JP3897923B2 (ja)	2007-03-28	毛髪化粧料の製造方法
CH627483A5 (fr)	1982-01-15	Procede de preparation de nouveaux oligomeres tensio-actifs sequences, du type polyethers polyhydroxyles, et compositions les contenant.
US4879399A (en)	1989-11-07	Ether sulfates of a mixture of branched 1-decanols
JP4760489B2 (ja)	2011-08-31	化粧料用基剤およびそれを配合してなる化粧料
GB2185488A (en)	1987-07-22	Alkoxylated decanol sulphate surfactants and their use in shampoo compositions
US4992211A (en)	1991-02-12	Alkylene oxide-containing amphoteric surfactants
CA2019551A1 (fr)	1990-12-22	Composes quaternarises contenant de l'azote
JPH0115482B2 (fr)	1989-03-17
JP3525848B2 (ja)	2004-05-10	アニオン性界面活性剤及び洗浄剤組成物
WO1998037062A1 (fr)	1998-08-27	Nouveaux tensioactifs non ioniques jumeles de nonylphenol
US4678665A (en)	1987-07-07	Polyanionic compounds derived from aromatic ethers of polyglycerols
GB2226557A (en)	1990-07-04	Alkeline oxide-containing amphoteric surfactants
JPH0586367B2 (fr)	1993-12-10
US4290956A (en)	1981-09-22	Tensio-active polypod compounds, process for preparing them and compositions containing them
JPS62257932A (ja)	1987-11-10	アルキルポリオキシアルキレンカルボキシレ−トエステル
EP0621265B1 (fr)	1997-01-22	Sulfate de N-alkylcarbamylalkanol ou son sel, son procédé de préparation et composition détergent le contenant