CH670085A5 - - Google Patents

Download PDF

Info

Publication number: CH670085A5
Authority: CH; Switzerland
Prior art keywords: integer; alkyl; alcohol; formula; compounds
Prior art date: 1986-04-30

Application number

CH1599/87A

Other languages

German (de)

English (en)

Inventor

Robert V Casciani

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.)

1986-04-30

Filing date

1987-04-27

Publication date

1989-05-12

1987-04-27 Application filed by Sandoz Ag filed Critical Sandoz Ag

1989-05-12 Publication of CH670085A5 publication Critical patent/CH670085A5/de

Links

150000001875 compounds Chemical class 0.000 claims description 44
125000000217 alkyl group Chemical group 0.000 claims description 11
239000003995 emulsifying agent Substances 0.000 claims description 7
239000000314 lubricant Substances 0.000 claims description 4
239000000203 mixture Substances 0.000 description 32
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
239000000047 product Substances 0.000 description 18
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 16
238000006243 chemical reaction Methods 0.000 description 11
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 9
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
239000002253 acid Substances 0.000 description 9
239000003795 chemical substances by application Substances 0.000 description 9
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 8
-1 lithium aluminum hydride Chemical compound 0.000 description 8
HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 8
239000007795 chemical reaction product Substances 0.000 description 7
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
239000006210 lotion Substances 0.000 description 6
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
239000000654 additive Substances 0.000 description 5
150000001298 alcohols Chemical class 0.000 description 5
239000003054 catalyst Substances 0.000 description 5
239000006071 cream Substances 0.000 description 5
238000000034 method Methods 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 4
150000002191 fatty alcohols Chemical class 0.000 description 4
238000009472 formulation Methods 0.000 description 4
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 4
BXWNKGSJHAJOGX-UHFFFAOYSA-N n-hexadecyl alcohol Natural products CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
125000000913 palmityl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
239000004014 plasticizer Substances 0.000 description 4
239000012279 sodium borohydride Substances 0.000 description 4
229910000033 sodium borohydride Inorganic materials 0.000 description 4
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
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 3
239000002202 Polyethylene glycol Substances 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
229960000541 cetyl alcohol Drugs 0.000 description 3
239000013065 commercial product Substances 0.000 description 3
239000000470 constituent Substances 0.000 description 3
230000032050 esterification Effects 0.000 description 3
238000005886 esterification reaction Methods 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 3
229920001223 polyethylene glycol Polymers 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
229960000583 acetic acid Drugs 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
238000009835 boiling Methods 0.000 description 2
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
229940106681 chloroacetic acid Drugs 0.000 description 2
239000002537 cosmetic Substances 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
239000007789 gas Substances 0.000 description 2
239000012362 glacial acetic acid Substances 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
239000000543 intermediate Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000004292 methyl p-hydroxybenzoate Substances 0.000 description 2
235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 2
229960002216 methylparaben Drugs 0.000 description 2
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 2
239000003921 oil Substances 0.000 description 2
235000019198 oils Nutrition 0.000 description 2
239000004006 olive oil Substances 0.000 description 2
235000008390 olive oil Nutrition 0.000 description 2
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
239000011814 protection agent Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
229920002545 silicone oil Polymers 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
239000004753 textile Substances 0.000 description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
150000000209 1-decanols Chemical class 0.000 description 1
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
STZSATRZAOXIOR-UHFFFAOYSA-N 4-amino-2,3-dimethyl-5-octylbenzoic acid Chemical compound CCCCCCCCC1=CC(C(O)=O)=C(C)C(C)=C1N STZSATRZAOXIOR-UHFFFAOYSA-N 0.000 description 1
PLLBRTOLHQQAQQ-UHFFFAOYSA-N 8-methylnonan-1-ol Chemical compound CC(C)CCCCCCCO PLLBRTOLHQQAQQ-UHFFFAOYSA-N 0.000 description 1
229910015900 BF3 Inorganic materials 0.000 description 1
NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
239000004440 Isodecyl alcohol Substances 0.000 description 1
239000004909 Moisturizer Substances 0.000 description 1
VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
229920001214 Polysorbate 60 Polymers 0.000 description 1
HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
239000003377 acid catalyst Substances 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000012790 adhesive layer Substances 0.000 description 1
239000002390 adhesive tape Substances 0.000 description 1
239000003905 agrochemical Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
238000010533 azeotropic distillation Methods 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
230000003750 conditioning effect Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
125000002704 decyl group Chemical group [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])* 0.000 description 1
239000004205 dimethyl polysiloxane Substances 0.000 description 1
235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
239000000975 dye Substances 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000007046 ethoxylation reaction Methods 0.000 description 1
239000003925 fat Substances 0.000 description 1
239000012467 final product Substances 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
150000008040 ionic compounds Chemical class 0.000 description 1
XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
239000010985 leather Substances 0.000 description 1
239000012280 lithium aluminium hydride Substances 0.000 description 1
239000010687 lubricating oil Substances 0.000 description 1
239000000155 melt Substances 0.000 description 1
229940041616 menthol Drugs 0.000 description 1
230000011987 methylation Effects 0.000 description 1
238000007069 methylation reaction Methods 0.000 description 1
230000001333 moisturizer Effects 0.000 description 1
230000003020 moisturizing effect Effects 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
239000012875 nonionic emulsifier Substances 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
239000003973 paint Substances 0.000 description 1
239000000123 paper Substances 0.000 description 1
235000011837 pasties Nutrition 0.000 description 1
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920000136 polysorbate Polymers 0.000 description 1
229950008882 polysorbate Drugs 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
150000003138 primary alcohols Chemical class 0.000 description 1
239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
229960003415 propylparaben Drugs 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
239000000376 reactant Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
230000000630 rising effect Effects 0.000 description 1
239000005060 rubber Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000007787 solid Substances 0.000 description 1
230000000475 sunscreen effect Effects 0.000 description 1
239000000516 sunscreening agent Substances 0.000 description 1
230000003655 tactile properties Effects 0.000 description 1
239000001993 wax Substances 0.000 description 1
239000011787 zinc oxide Substances 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
- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/86—Polyethers
- 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
- C07C69/708—Ethers

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Chemical & Material Sciences (AREA)
Birds (AREA)
Epidemiology (AREA)
Emergency Medicine (AREA)
Dermatology (AREA)
Cosmetics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Compositions Of Macromolecular Compounds (AREA)
Polyethers (AREA)

CH1599/87A 1986-04-30 1987-04-27 CH670085A5 (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US85768386A	1986-04-30	1986-04-30

Publications (1)

Publication Number	Publication Date
CH670085A5 true CH670085A5 (fr)	1989-05-12

Family

ID=25326519

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1599/87A CH670085A5 (fr)	1986-04-30	1987-04-27

Country Status (9)

Country	Link
JP (1)	JPH0832778B2 (fr)
CH (1)	CH670085A5 (fr)
DE (1)	DE3712646C2 (fr)
FR (1)	FR2598707B1 (fr)
GB (1)	GB2189787B (fr)
HK (1)	HK15794A (fr)
IT (1)	IT1216806B (fr)
NL (1)	NL8700988A (fr)
SG (1)	SG112992G (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3932989A1 (de) *	1989-10-03	1991-04-11	Espe Stiftung	Polyalkylenoxidderivate enthaltende polyetherabformmassen
DE3924201A1 (de) *	1989-07-21	1991-01-24	Henkel Kgaa	Oberflaechenaktive ethercarbonsaeure-polyolester
DE19928128C1 (de) *	1999-06-19	2000-11-30	Clariant Gmbh	Verfahren zur Herstellung von Ethercarbonsäuren mit niedrigem Restalkohol
JP5035581B2 (ja) *	2001-09-27	2012-09-26	日油株式会社	アルキレンオキシド誘導体の製造方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2109947A (en) *	1934-01-27	1938-03-01	Margaret R North	Ether acid esters of higher alcohols
US2803646A (en) *	1953-10-23	1957-08-20	Jefferson Chem Co Inc	Process of producing ether-esters
FR1438235A (fr) *	1964-10-05	1966-05-13	Oreal	Nouveaux émulsionnants, émulsions et produits cosmétiques en résultant
LU47604A1 (fr) *	1964-12-17	1966-06-17
LU70720A1 (fr) *	1974-08-12	1976-08-19
SE403611B (sv) *	1975-09-05	1978-08-28	Berol Kemi Ab	Forfarande for framstellning av en reaktionsprodukt mellan en epoxid och en organisk forening innehallande reaktivt vete i nervaro av viss angiven katalysator

1987
- 1987-04-14 DE DE3712646A patent/DE3712646C2/de not_active Expired - Lifetime
- 1987-04-24 FR FR878705894A patent/FR2598707B1/fr not_active Expired - Lifetime
- 1987-04-27 IT IT8747888A patent/IT1216806B/it active
- 1987-04-27 NL NL8700988A patent/NL8700988A/nl not_active Application Discontinuation
- 1987-04-27 CH CH1599/87A patent/CH670085A5/de not_active IP Right Cessation
- 1987-04-28 JP JP62103398A patent/JPH0832778B2/ja not_active Expired - Lifetime
- 1987-04-28 GB GB8710060A patent/GB2189787B/en not_active Expired - Lifetime
1992
- 1992-11-02 SG SG1129/92A patent/SG112992G/en unknown
1994
- 1994-02-24 HK HK157/94A patent/HK15794A/xx not_active IP Right Cessation

Also Published As

Publication number	Publication date
NL8700988A (nl)	1987-11-16
DE3712646A1 (de)	1987-11-05
GB2189787B (en)	1990-02-14
DE3712646C2 (de)	1996-07-25
JPS62257932A (ja)	1987-11-10
JPH0832778B2 (ja)	1996-03-29
GB8710060D0 (en)	1987-06-03
HK15794A (en)	1994-03-04
IT8747888A0 (it)	1987-04-27
IT1216806B (it)	1990-03-14
FR2598707B1 (fr)	1990-03-30
SG112992G (en)	1992-12-24
GB2189787A (en)	1987-11-04
FR2598707A1 (fr)	1987-11-20

Legal Events

Date	Code	Title	Description
1996-07-15	NV	New agent	Representative=s name: SANDOZ TECHNOLOGIE AG
1996-07-15	PUE	Assignment	Owner name: SANDOZ AG TRANSFER- SANDOZ AG;CLARIANT FINANCE (BV
1997-03-14	NV	New agent	Representative=s name: CLARIANT INTERNATIONAL LTD.
1999-12-15	PL	Patent ceased

Publication	Publication Date	Title
DE60038268T2 (de)	2009-03-19	Kosmetische Zubereitungen
EP0582246B1 (fr)	1997-01-22	Mélange d'esters d'acides gras et de polyglycérine
DE69529470T2 (de)	2003-07-31	Emulgiermittelzusammensetzungen auf basis von fettalkohol- phosphatestern
DE3035135C2 (fr)	1990-03-22
US4766153A (en)	1988-08-23	Alkyl polyoxyalkylene carboxylate esters and skin care compositions containing the same
DE2353088C3 (de)	1980-06-19	Gemische aus N-Acyl-asparaginsäurediestem und Gemische aus N-Acylglutaminsäure-diestern sowie diese Gemische enthaltende öllösliche nichtionische oberflächenaktive Mittel und kosmetische Mittel
EP0579159A2 (fr)	1994-01-19	Procédé de préparation de mélanges à base d'esters polyglycéroliques d'acides gras et leurs utilisations dans des préparations cosmétiques, pharmaceutiques et chimico-techniques
EP0499700B1 (fr)	1995-07-19	Mélange d'esters d'acides gras et de polyglycérine
DE2455287C3 (de)	1987-12-03	Verwendung von Wasser- in-Öl-Emulgatoren
EP0668853B1 (fr)	1997-04-02	Derives de l'acide succinique utilises comme agents pour le conditionnement de la peau
DE60200495T2 (de)	2005-05-19	Polyethylenglykol und Verfahren zu dessen Herstellung
DE2256526C3 (de)	1982-03-25	Nicht-ionische polyhydroxylierte grenzflächenaktive Verbindungen, Verfahren zu deren Herstellung und daraus erhaltene Mittel
DE3427093C2 (de)	1995-03-30	Neue Polyolether-Verbindungen, Verfahren zur Herstellung derselben und Kosmetika mit einem Gehalt derselben
EP0143245B1 (fr)	1988-02-24	Emulsifiants O/W pour usages cosmétiques
DE2535777A1 (de)	1976-02-26	Nue polyaether und deren verwendung in der kosmetologie
EP0072988A1 (fr)	1983-03-02	Utilisation de 1,3-Dialkylcyclohexanes comme composant huileux cosmétique
DE2752116C2 (de)	1984-07-12	Salze von N-[N',N'-Bis(2-carboxyethyl)-aminoethyl]-N-(2-hydroxyethyl)-carbonsäureamiden, Verfahren zu ihrer Herstellung und ihre Verwendung als grenzflächenaktive Stoffe
DE3835199A1 (de)	1990-04-19	Substituierte glucoside
CH670085A5 (fr)	1989-05-12
US4399297A (en)	1983-08-16	Polyalkoxycarbinol cinnamates and protective sun agents containing these compounds
EP0008105B1 (fr)	1982-03-03	Utilisation d'esters d'acide citrique dans des préparations cosmétiques
CH668266A5 (de)	1988-12-15	Tensid-gemische.
DE69600014T2 (de)	1997-07-24	Verwendung einer Fluorkohlenwasserstoffverbindung in einer Emulsion, diese enthaltende Emulsion und Zusammensetzung
EP0513134B1 (fr)	1994-08-17	Ester d'acide hydroxycarboxylique sulfate
DE3417819A1 (de)	1985-11-14	Blockcopolymere polyglycolether als loesungsvermittler fuer oelloesliche parfuemoele