JPH0832778B2 - 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 - Google Patents

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

Info

Publication number: JPH0832778B2
Authority: JP; Japan
Prior art keywords: integer; alkyl; alcohol; formula; compound
Prior art date: 1986-04-30
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.): Expired - Lifetime

Application number

JP62103398A

Other languages

English (en)

Japanese (ja)

Other versions

JPS62257932A (ja

Inventor

ブイ．カシアーニロバート

Original Assignee

サンドアクチエンゲゼルシヤフト

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

1987-04-28

Publication date

1996-03-29

1987-04-28 Application filed by サンドアクチエンゲゼルシヤフト filed Critical サンドアクチエンゲゼルシヤフト

1987-11-10 Publication of JPS62257932A publication Critical patent/JPS62257932A/ja

1996-03-29 Publication of JPH0832778B2 publication Critical patent/JPH0832778B2/ja

2011-03-29 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

125000000217 alkyl group Chemical group 0.000 title claims description 35
-1 carboxylate ester Chemical class 0.000 title description 20
239000000203 mixture Substances 0.000 claims description 53
150000001875 compounds Chemical class 0.000 claims description 52
150000001298 alcohols Chemical class 0.000 claims description 10
239000003974 emollient agent Substances 0.000 claims description 7
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 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 claims description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 23
238000006243 chemical reaction Methods 0.000 description 21
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 20
239000004615 ingredient Substances 0.000 description 12
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 11
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 10
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 10
238000000034 method Methods 0.000 description 10
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
239000003054 catalyst Substances 0.000 description 8
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 8
239000011541 reaction mixture Substances 0.000 description 8
HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 8
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical group S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
150000001732 carboxylic acid derivatives Chemical class 0.000 description 6
239000003995 emulsifying agent Substances 0.000 description 6
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
239000000126 substance Substances 0.000 description 6
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
239000002253 acid Substances 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
238000003756 stirring Methods 0.000 description 5
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
238000010908 decantation Methods 0.000 description 4
239000007788 liquid Substances 0.000 description 4
239000006210 lotion Substances 0.000 description 4
239000000314 lubricant Substances 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
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 4
239000012279 sodium borohydride Substances 0.000 description 4
229910000033 sodium borohydride Inorganic materials 0.000 description 4
239000005968 1-Decanol Substances 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
239000002202 Polyethylene glycol Substances 0.000 description 3
125000003158 alcohol group Chemical group 0.000 description 3
238000009835 boiling Methods 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
229960000541 cetyl alcohol Drugs 0.000 description 3
238000001816 cooling Methods 0.000 description 3
125000003438 dodecyl 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])C([H])([H])C([H])([H])* 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
150000002191 fatty alcohols Chemical class 0.000 description 3
150000002194 fatty esters Chemical class 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
239000000463 material Substances 0.000 description 3
239000003921 oil Substances 0.000 description 3
235000019198 oils Nutrition 0.000 description 3
229920001223 polyethylene glycol Polymers 0.000 description 3
150000003138 primary alcohols Chemical class 0.000 description 3
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
229960000583 acetic acid Drugs 0.000 description 2
230000002378 acidificating effect Effects 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000029936 alkylation Effects 0.000 description 2
238000005804 alkylation reaction Methods 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
125000004181 carboxyalkyl group Chemical group 0.000 description 2
150000007942 carboxylates Chemical class 0.000 description 2
239000003638 chemical reducing agent Substances 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
239000002537 cosmetic Substances 0.000 description 2
239000006071 cream Substances 0.000 description 2
238000004821 distillation Methods 0.000 description 2
230000032050 esterification Effects 0.000 description 2
238000005886 esterification reaction Methods 0.000 description 2
239000012530 fluid Substances 0.000 description 2
239000012362 glacial acetic acid Substances 0.000 description 2
239000003906 humectant 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
239000004006 olive oil Substances 0.000 description 2
235000008390 olive oil Nutrition 0.000 description 2
239000008188 pellet Substances 0.000 description 2
239000000047 product Substances 0.000 description 2
239000004405 propyl p-hydroxybenzoate Substances 0.000 description 2
235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 2
229960003415 propylparaben Drugs 0.000 description 2
238000010992 reflux Methods 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
229920002545 silicone oil Polymers 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
230000003655 tactile properties Effects 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
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
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
PSBDWGZCVUAZQS-UHFFFAOYSA-N (dimethylsulfonio)acetate Chemical compound C[S+](C)CC([O-])=O PSBDWGZCVUAZQS-UHFFFAOYSA-N 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
MCFBUIIRFZBRCU-UHFFFAOYSA-N 4-[1-[5-[6-(trifluoromethyl)-1h-benzimidazol-2-yl]pyridin-2-yl]piperidin-4-yl]oxycyclohexane-1-carboxylic acid Chemical compound C1CC(C(=O)O)CCC1OC1CCN(C=2N=CC(=CC=2)C=2NC3=CC(=CC=C3N=2)C(F)(F)F)CC1 MCFBUIIRFZBRCU-UHFFFAOYSA-N 0.000 description 1
HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
229910015900 BF3 Inorganic materials 0.000 description 1
KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 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
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
239000004909 Moisturizer Substances 0.000 description 1
KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 1
229920001214 Polysorbate 60 Polymers 0.000 description 1
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
239000004902 Softening Agent Substances 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
238000006959 Williamson synthesis reaction Methods 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
239000012790 adhesive layer Substances 0.000 description 1
239000002390 adhesive tape Substances 0.000 description 1
239000008135 aqueous vehicle Substances 0.000 description 1
238000010533 azeotropic distillation Methods 0.000 description 1
229960003237 betaine Drugs 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
GUPWNYUKYICHQX-UHFFFAOYSA-N carbonobromidic acid Chemical compound OC(Br)=O GUPWNYUKYICHQX-UHFFFAOYSA-N 0.000 description 1
125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000003982 chlorocarboxylic acids Chemical class 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
230000003750 conditioning effect Effects 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000010730 cutting oil Substances 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
229940079593 drug Drugs 0.000 description 1
239000003814 drug Substances 0.000 description 1
239000000975 dye Substances 0.000 description 1
230000000694 effects Effects 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
229960004279 formaldehyde Drugs 0.000 description 1
235000019256 formaldehyde Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000007789 gas Substances 0.000 description 1
230000005484 gravity Effects 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
238000011221 initial treatment Methods 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
239000004922 lacquer Substances 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
229940041616 menthol Drugs 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
230000001333 moisturizer Effects 0.000 description 1
230000003020 moisturizing effect Effects 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
239000000123 paper Substances 0.000 description 1
239000002304 perfume Substances 0.000 description 1
239000003209 petroleum derivative Substances 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
239000002243 precursor Substances 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000003333 secondary alcohols Chemical class 0.000 description 1
239000002884 skin cream Substances 0.000 description 1
FDRCDNZGSXJAFP-UHFFFAOYSA-M sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
229940117986 sulfobetaine Drugs 0.000 description 1
230000000475 sunscreen effect Effects 0.000 description 1
239000000516 sunscreening agent Substances 0.000 description 1
238000011282 treatment Methods 0.000 description 1
239000000341 volatile oil Substances 0.000 description 1
239000001993 wax Substances 0.000 description 1
239000000080 wetting agent 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)

JP62103398A 1986-04-30 1987-04-28 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 Expired - Lifetime JPH0832778B2 (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US85768386A	1986-04-30	1986-04-30
US857683		1986-04-30

Publications (2)

Publication Number	Publication Date
JPS62257932A JPS62257932A (ja)	1987-11-10
JPH0832778B2 true JPH0832778B2 (ja)	1996-03-29

Family

ID=25326519

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP62103398A Expired - Lifetime JPH0832778B2 (ja)	1986-04-30	1987-04-28	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

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
CH670085A5 (fr)	1989-05-12
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
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CA2092360C (fr)	2000-07-18	Esters alcoxylates gras d'acides aliphatiques ou aromatiques dicarboxyliques et tricarboxyliques
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JPS6334851B2 (fr)	1988-07-12
EP0028457B1 (fr)	1984-03-07	Composition cosmétique et émulsifiante
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JP3812149B2 (ja)	2006-08-23	化粧品用乳化剤
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JPH08119826A (ja)	1996-05-14	化粧料
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CA2146422C (fr)	1998-06-30	Compositions non aqueuses adoucissantes pour applications topiques