CH650764A5 - Alkyl-polyoxyalkylen-carboxylate. - Google Patents

Alkyl-polyoxyalkylen-carboxylate. Download PDF

Info

Publication number: CH650764A5
Authority: CH; Switzerland
Prior art keywords: compounds; formula; alkyl; sodium; parts
Prior art date: 1980-11-28

Application number

CH7354/81A

Other languages

German (de)

English (en)

Inventor

Harold Paul Dr Wolf

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.)

1980-11-28

Filing date

1981-11-16

Publication date

1985-08-15

1981-11-16 Application filed by Sandoz Ag filed Critical Sandoz Ag

1985-08-15 Publication of CH650764A5 publication Critical patent/CH650764A5/de

Links

150000007942 carboxylates Chemical class 0.000 title description 3
150000001875 compounds Chemical class 0.000 description 39
238000002360 preparation method Methods 0.000 description 13
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
239000000203 mixture Substances 0.000 description 12
239000004094 surface-active agent Substances 0.000 description 10
229910052783 alkali metal Inorganic materials 0.000 description 9
-1 alkyl radicals Chemical class 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 9
239000001257 hydrogen Substances 0.000 description 9
229910052739 hydrogen Inorganic materials 0.000 description 9
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 8
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 8
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 8
239000013543 active substance Substances 0.000 description 8
150000001340 alkali metals Chemical class 0.000 description 8
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 7
239000002253 acid Substances 0.000 description 7
125000000217 alkyl group Chemical group 0.000 description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
229910052757 nitrogen Inorganic materials 0.000 description 7
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
150000001768 cations Chemical class 0.000 description 6
239000011734 sodium Substances 0.000 description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
239000000654 additive Substances 0.000 description 5
239000013067 intermediate product Substances 0.000 description 5
229910052708 sodium Inorganic materials 0.000 description 5
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 4
229910052784 alkaline earth metal Inorganic materials 0.000 description 4
150000001342 alkaline earth metals Chemical class 0.000 description 4
239000007795 chemical reaction product Substances 0.000 description 4
239000003599 detergent Substances 0.000 description 4
150000002431 hydrogen Chemical class 0.000 description 4
238000000034 method Methods 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
229910052700 potassium Inorganic materials 0.000 description 4
239000011591 potassium Substances 0.000 description 4
239000000047 product Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
125000002947 alkylene group Chemical group 0.000 description 3
125000000129 anionic group Chemical group 0.000 description 3
239000000543 intermediate Substances 0.000 description 3
ZSIAUFGUXNUGDI-UHFFFAOYSA-N n-hexyl alcohol Natural products CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
241000251730 Chondrichthyes Species 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
150000008044 alkali metal hydroxides Chemical class 0.000 description 2
229910052788 barium Inorganic materials 0.000 description 2
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
239000011575 calcium Substances 0.000 description 2
239000001768 carboxy methyl cellulose Substances 0.000 description 2
239000003638 chemical reducing agent Substances 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
229910052744 lithium Inorganic materials 0.000 description 2
229910052749 magnesium Inorganic materials 0.000 description 2
239000011777 magnesium Substances 0.000 description 2
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-O morpholinium Chemical compound [H+].C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-O 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 2
239000012279 sodium borohydride Substances 0.000 description 2
229910000033 sodium borohydride Inorganic materials 0.000 description 2
239000007787 solid Substances 0.000 description 2
LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
KHJWSKNOMFJTDN-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetic acid;sodium Chemical compound [Na].OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KHJWSKNOMFJTDN-UHFFFAOYSA-N 0.000 description 1
ATACSYDDCNWCLV-UHFFFAOYSA-N 2-chloroacetic acid;sodium Chemical compound [Na].OC(=O)CCl ATACSYDDCNWCLV-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
102000004190 Enzymes Human genes 0.000 description 1
108090000790 Enzymes Proteins 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
241001274216 Naso Species 0.000 description 1
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
235000019482 Palm oil Nutrition 0.000 description 1
102000035195 Peptidases Human genes 0.000 description 1
108091005804 Peptidases Proteins 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
229920000388 Polyphosphate Polymers 0.000 description 1
239000004115 Sodium Silicate Substances 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 1
229960000583 acetic acid Drugs 0.000 description 1
DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
239000007844 bleaching agent Substances 0.000 description 1
KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
239000012459 cleaning agent Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
235000011180 diphosphates Nutrition 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004043 dyeing Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
229940088598 enzyme Drugs 0.000 description 1
239000002979 fabric softener Substances 0.000 description 1
239000003925 fat Substances 0.000 description 1
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
239000007850 fluorescent dye Substances 0.000 description 1
238000011010 flushing procedure Methods 0.000 description 1
239000006260 foam Substances 0.000 description 1
239000003205 fragrance Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000012362 glacial acetic acid Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
239000008233 hard water Substances 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
150000008040 ionic compounds Chemical class 0.000 description 1
239000010985 leather Substances 0.000 description 1
239000012280 lithium aluminium hydride Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
KJIOQYGWTQBHNH-UHFFFAOYSA-N methyl butylhexanol Natural products CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
ZWRUINPWMLAQRD-UHFFFAOYSA-N n-Nonyl alcohol Natural products CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 1
MWKFXSUHUHTGQN-UHFFFAOYSA-N n-decyl alcohol Natural products CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
150000002895 organic esters Chemical class 0.000 description 1
230000020477 pH reduction Effects 0.000 description 1
239000002540 palm oil Substances 0.000 description 1
239000000123 paper Substances 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
229920005646 polycarboxylate Polymers 0.000 description 1
239000001205 polyphosphate Substances 0.000 description 1
235000011176 polyphosphates Nutrition 0.000 description 1
239000002243 precursor Substances 0.000 description 1
150000003138 primary alcohols Chemical class 0.000 description 1
229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
229910001415 sodium ion Inorganic materials 0.000 description 1
229910001948 sodium oxide Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
235000019832 sodium triphosphate Nutrition 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000003784 tall oil Substances 0.000 description 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 description 1
239000004753 textile Substances 0.000 description 1
238000009988 textile finishing Methods 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/08—Polycarboxylic acids containing no nitrogen or sulfur
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/125—Saturated compounds having only one carboxyl group and containing ether groups, groups, groups, or groups

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Detergent Compositions (AREA)

CH7354/81A 1980-11-28 1981-11-16 Alkyl-polyoxyalkylen-carboxylate. CH650764A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US21109980A	1980-11-28	1980-11-28

Publications (1)

Publication Number	Publication Date
CH650764A5 true CH650764A5 (de)	1985-08-15

Family

ID=22785588

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH7354/81A CH650764A5 (de)	1980-11-28	1981-11-16	Alkyl-polyoxyalkylen-carboxylate.

Country Status (7)

Country	Link
CH (1)	CH650764A5 (it)
DE (1)	DE3145776A1 (it)
FR (1)	FR2495168B1 (it)
GB (1)	GB2088863B (it)
HK (1)	HK90487A (it)
IT (1)	IT1172092B (it)
SG (1)	SG62687G (it)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4415062A1 (de) *	1994-04-29	1995-11-02	Stockhausen Chem Fab Gmbh	Mittel und Verfahren zur Hydrophobierung von Ledern und Pelzen

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL8301389A (nl) *	1983-04-20	1984-11-16	Chem Y	Nieuwe vloeibare jodoforen.
US4533485A (en) *	1983-06-20	1985-08-06	Olin Corporation	Anionic surfactant addition products of maleic or fumaric acid and a poly(oxyalkylated) alcohol
CA1279874C (en) *	1983-10-28	1991-02-05	Chevron Research And Technology Company	Stable emulsifier and substituted succinic anhydride compositions therewith
US4692551A (en) *	1986-07-23	1987-09-08	Gaf Corporation	Preparation of carboxypropylated non-ionic surfactants
US5250203A (en) *	1987-02-27	1993-10-05	The Lubrizol Corporation	Lubricating oil compositions containing a polyoxyalkylene carboxylic acid salt additive
US4784781A (en) *	1987-02-27	1988-11-15	The Lubrizol Corporation	Lubricating oil compositions containing multi-functional additive component
DE3861820D1 (de) *	1987-05-13	1991-04-04	Sanyo Chemical Ind Ltd	Carbonsaeuren und verfahren zur herstellung derselben.
ES2032596T3 (es) *	1987-07-14	1993-02-16	Ciba-Geigy Ag	Composiciones inhibidoras de corrosion.
DE3903663C1 (it) *	1989-02-08	1990-09-27	Huels Ag, 4370 Marl, De
DE4225626A1 (de) *	1992-08-03	1994-02-10	Henkel Kgaa	Verwendung von Ethercarbonsäuren als keimtötende Substanzen
DE4236697A1 (de) *	1992-10-30	1994-05-05	Henkel Kgaa	Trockenstoffe für oxidativ trocknende Lacke
GB9407778D0 (en) *	1994-04-20	1994-06-15	Sandoz Ltd	Improvements in or relating to organic compounds
DE19928128C1 (de) *	1999-06-19	2000-11-30	Clariant Gmbh	Verfahren zur Herstellung von Ethercarbonsäuren mit niedrigem Restalkohol
US9605198B2 (en)	2011-09-15	2017-03-28	Chevron U.S.A. Inc.	Mixed carbon length synthesis of primary Guerbet alcohols
US12338382B2 (en) *	2017-04-04	2025-06-24	Harcros Chemicals, Inc.	Surfactants having non-conventional hydrophobes

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2323483A1 (de) *	1973-05-10	1974-11-28	Huels Chemische Werke Ag	Verwendung von mischungen aus alkylpolyaethercarbonsaeuresalzen und alkylpolyglykolaethern in wasch- und reinigungsmitteln
US4039683A (en) *	1973-08-21	1977-08-02	Merck Patent Gesellschaft Mit Beschrankter Haftung	Phenoxypropionic acid derivatives and pharmaceutical preparations containing same
DE2754210A1 (de) *	1976-12-10	1978-06-15	Procter & Gamble	Oberflaechenaktives mittel auf basis von carboxyalkylierten alkylpolyethern

1981
- 1981-11-16 CH CH7354/81A patent/CH650764A5/de not_active IP Right Cessation
- 1981-11-19 DE DE19813145776 patent/DE3145776A1/de not_active Withdrawn
- 1981-11-19 FR FR8121930A patent/FR2495168B1/fr not_active Expired
- 1981-11-24 IT IT49759/81A patent/IT1172092B/it active
- 1981-11-24 GB GB8135382A patent/GB2088863B/en not_active Expired
1987
- 1987-08-03 SG SG626/87A patent/SG62687G/en unknown
- 1987-12-03 HK HK904/87A patent/HK90487A/xx unknown

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4415062A1 (de) *	1994-04-29	1995-11-02	Stockhausen Chem Fab Gmbh	Mittel und Verfahren zur Hydrophobierung von Ledern und Pelzen
DE4415062B4 (de) *	1994-04-29	2004-04-01	Stockhausen Gmbh & Co. Kg	Mittel und Verfahren zur Hydrophobierung von Ledern und Pelzen

Also Published As

Publication number	Publication date
FR2495168B1 (fr)	1986-05-16
IT8149759A0 (it)	1981-11-24
GB2088863A (en)	1982-06-16
SG62687G (en)	1987-11-13
GB2088863B (en)	1984-08-22
FR2495168A1 (fr)	1982-06-04
IT1172092B (it)	1987-06-18
DE3145776A1 (de)	1982-07-08
HK90487A (en)	1987-12-11

Legal Events

Date	Code	Title	Description
1995-07-31	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
CH650764A5 (de)	1985-08-15	Alkyl-polyoxyalkylen-carboxylate.
DE69310926T2 (de)	1997-08-28	2-propylheptanol-derivate und deren verwendung
EP1501776B2 (de)	2016-10-12	C10-alkanolalkoxylate und ihre verwendung
DE2657518A1 (de)	1977-07-07	Neue verbindungen und dieselben enthaltende detergensgemische
DE2900232C2 (de)	1985-04-11	Flüssiges Reinigungsmittel
DE10035617A1 (de)	2002-01-31	Sekundäre C¶1¶¶0¶-C¶1¶¶8¶-Tensidalkohole
DE4137317A1 (de)	1993-05-19	Ester von fettsaeuren mit ethoxylierten polyolen
DE3603580A1 (de)	1987-08-13	Estersulfonathaltige tensid-konzentrate und ihre verwendung
DE10121723A1 (de)	2002-11-07	Geminitenside
DE10348420A1 (de)	2005-05-25	C10-Alkanolalkoxylat-Gemische und ihre Verwendung - Neue schaumarme Netzer
WO1991009925A2 (de)	1991-07-11	Verwendung einer kombination nichtionischer tenside
DE2257642A1 (de)	1974-06-20	Biologisch abbaubare wasch- und reinigungsmittel
EP2446008B1 (de)	2016-03-02	Verwendung von dietherverbindungen bei der chemischen reinigung von textil-, leder- oder pelzwaren
EP0576464A1 (de)	1994-01-05	Verfahren zur herstellung von hochkonzentrierten fettalkoholsulfat-pasten.
WO2011003904A1 (de)	2011-01-13	Tensidgemisch mit kurz- und langkettigen komponenten
DE2220503A1 (de)	1973-01-18	Wasch- und reinigungsmittel
EP0370273A1 (de)	1990-05-30	Neue Fettalkoholgemische und ihre Ethoxylate mit verbessertem Kälteverhalten
EP0079105B1 (de)	1985-06-19	Schaumkontrollierte Waschmittel
EP3250668B1 (de)	2020-04-29	Saures flüssigkompaktwaschmittel enthaltend hydroxycarbonsäure, niotensid und -amylase
CH635614A5 (en)	1983-04-15	Liquid detergent and process for its preparation
DE4418847A1 (de)	1995-12-07	Bleich- und Reinigungsmittel
DE4003096A1 (de)	1991-08-08	Sulfierte hydroxycarbonsaeureester
CH676604A5 (it)	1991-02-15
DE4041172A1 (de)	1992-06-25	Fluessige seifenzubereitung
EP0975719B1 (de)	2002-12-11	Verfahren zur herstellung von niedrigviskosen wässerigen alkyl(ether)sulfatpasten