DD295342A5 - Amidierte fettsaeuremischungen und deren verwendung als verdickungsmittel - Google Patents

Amidierte fettsaeuremischungen und deren verwendung als verdickungsmittel Download PDF

Info

Publication number: DD295342A5
Authority: DD; German Democratic Republic
Prior art keywords: fatty acid; thickener; rapeseed oil; fatty acids; thickeners
Prior art date: 1989-03-04

Application number

DD90344288A

Other languages

German (de)

English (en)

Inventor

Jacob K Smid

Reinout H Van Der Veen

Original Assignee

��@�K@�Kk��

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.)

1989-03-04

Filing date

1990-09-28

Publication date

1991-10-31

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=19854245&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=DD295342(A5) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1990-09-28 Application filed by ��@�K@�Kk�� filed Critical ��@�K@�Kk��

1991-10-31 Publication of DD295342A5 publication Critical patent/DD295342A5/de

Links

239000000203 mixture Substances 0.000 title claims abstract description 40
239000002562 thickening agent Substances 0.000 title abstract description 53
239000002253 acid Substances 0.000 title abstract 2
235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 52
229930195729 fatty acid Natural products 0.000 claims abstract description 52
239000000194 fatty acid Substances 0.000 claims abstract description 52
150000004665 fatty acids Chemical class 0.000 claims abstract description 51
239000003921 oil Substances 0.000 claims abstract description 15
241000196324 Embryophyta Species 0.000 claims abstract description 11
241000219198 Brassica Species 0.000 claims abstract description 10
235000011331 Brassica Nutrition 0.000 claims abstract description 8
125000000217 alkyl group Chemical group 0.000 claims abstract 2
DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 claims description 5
URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 claims description 5
DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
239000004094 surface-active agent Substances 0.000 abstract description 16
239000003599 detergent Substances 0.000 abstract description 15
125000004432 carbon atom Chemical group C* 0.000 abstract description 4
235000013830 Eruca Nutrition 0.000 abstract 1
241000801434 Eruca Species 0.000 abstract 1
231100000206 health hazard Toxicity 0.000 abstract 1
VQTGUFBGYOIUFS-UHFFFAOYSA-N nitrosylsulfuric acid Chemical class OS(=O)(=O)ON=O VQTGUFBGYOIUFS-UHFFFAOYSA-N 0.000 abstract 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 44
235000019484 Rapeseed oil Nutrition 0.000 description 34
239000011780 sodium chloride Substances 0.000 description 22
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
239000000243 solution Substances 0.000 description 14
235000019198 oils Nutrition 0.000 description 13
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 11
239000011541 reaction mixture Substances 0.000 description 10
229910052757 nitrogen Inorganic materials 0.000 description 9
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 7
238000007098 aminolysis reaction Methods 0.000 description 7
238000006243 chemical reaction Methods 0.000 description 7
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 7
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 6
230000000694 effects Effects 0.000 description 6
238000007046 ethoxylation reaction Methods 0.000 description 6
230000008719 thickening Effects 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
GIAFURWZWWWBQT-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol Chemical compound NCCOCCO GIAFURWZWWWBQT-UHFFFAOYSA-N 0.000 description 5
-1 2-aminoethoxy Chemical group 0.000 description 5
244000060011 Cocos nucifera Species 0.000 description 5
235000013162 Cocos nucifera Nutrition 0.000 description 5
235000019864 coconut oil Nutrition 0.000 description 5
239000003240 coconut oil Substances 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
239000000126 substance Substances 0.000 description 4
HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 3
CNDWHJQEGZZDTQ-UHFFFAOYSA-N 2-(2-amino-2-oxoethoxy)acetamide Chemical compound NC(=O)COCC(N)=O CNDWHJQEGZZDTQ-UHFFFAOYSA-N 0.000 description 3
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
YFCDLVPYFMHRQZ-UHFFFAOYSA-N N-Nitrosodiethanolamine Chemical compound OCCN(N=O)CCO YFCDLVPYFMHRQZ-UHFFFAOYSA-N 0.000 description 3
241000592344 Spermatophyta Species 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
239000013256 coordination polymer Substances 0.000 description 3
235000011187 glycerol Nutrition 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
240000007124 Brassica oleracea Species 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
238000001816 cooling Methods 0.000 description 2
239000002537 cosmetic Substances 0.000 description 2
230000007062 hydrolysis Effects 0.000 description 2
238000006460 hydrolysis reaction Methods 0.000 description 2
238000000034 method Methods 0.000 description 2
235000019508 mustard seed Nutrition 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
238000010926 purge Methods 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
LDMOEFOXLIZJOW-UHFFFAOYSA-N 1-dodecanesulfonic acid Chemical compound CCCCCCCCCCCCS(O)(=O)=O LDMOEFOXLIZJOW-UHFFFAOYSA-N 0.000 description 1
229940046305 5-bromo-5-nitro-1,3-dioxane Drugs 0.000 description 1
235000006463 Brassica alba Nutrition 0.000 description 1
244000060924 Brassica campestris Species 0.000 description 1
235000005637 Brassica campestris Nutrition 0.000 description 1
235000003351 Brassica cretica Nutrition 0.000 description 1
235000011371 Brassica hirta Nutrition 0.000 description 1
240000002791 Brassica napus Species 0.000 description 1
235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
240000008100 Brassica rapa Species 0.000 description 1
235000011292 Brassica rapa Nutrition 0.000 description 1
235000003343 Brassica rupestris Nutrition 0.000 description 1
235000004977 Brassica sinapistrum Nutrition 0.000 description 1
241000219193 Brassicaceae Species 0.000 description 1
LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 description 1
JYOQAMIUHGMNKV-UHFFFAOYSA-N COCOC.[Na] Chemical compound COCOC.[Na] JYOQAMIUHGMNKV-UHFFFAOYSA-N 0.000 description 1
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
241000220261 Sinapis Species 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
239000008186 active pharmaceutical agent Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
XVBRCOKDZVQYAY-UHFFFAOYSA-N bronidox Chemical compound [O-][N+](=O)C1(Br)COCOC1 XVBRCOKDZVQYAY-UHFFFAOYSA-N 0.000 description 1
230000000711 cancerogenic effect Effects 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
230000007423 decrease Effects 0.000 description 1
238000004851 dishwashing Methods 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
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 1
QVBODZPPYSSMEL-UHFFFAOYSA-N dodecyl sulfate;2-hydroxyethylazanium Chemical compound NCCO.CCCCCCCCCCCCOS(O)(=O)=O QVBODZPPYSSMEL-UHFFFAOYSA-N 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002169 ethanolamines Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
238000011010 flushing procedure Methods 0.000 description 1
239000006260 foam Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
150000002314 glycerols Chemical class 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
239000012535 impurity Substances 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000006210 lotion Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
150000002826 nitrites Chemical class 0.000 description 1
150000004005 nitrosamines Chemical class 0.000 description 1
235000011837 pasties Nutrition 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
238000000746 purification Methods 0.000 description 1
239000010499 rapseed oil Substances 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
244000128879 sarson Species 0.000 description 1
239000002453 shampoo Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
239000010913 used oil Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/16—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
- C07C233/17—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/18—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/16—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
- C07C233/17—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/20—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a carbon atom of an acyclic unsaturated carbon skeleton
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/32—Amides; Substituted amides

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Materials Engineering (AREA)
Detergent Compositions (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DD90344288A 1989-03-04 1990-09-28 Amidierte fettsaeuremischungen und deren verwendung als verdickungsmittel DD295342A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
NL8900539A NL8900539A (nl)	1989-03-04	1989-03-04	Geamideerde vetzuurmengsels en toepassing daarvan als verdikkingsmiddelen.

Publications (1)

Publication Number	Publication Date
DD295342A5 true DD295342A5 (de)	1991-10-31

Family

ID=19854245

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD90344288A DD295342A5 (de)	1989-03-04	1990-09-28	Amidierte fettsaeuremischungen und deren verwendung als verdickungsmittel

Country Status (8)

Country	Link
US (1)	US5124079A (es)
EP (1)	EP0386826B2 (es)
AT (1)	ATE105280T1 (es)
DD (1)	DD295342A5 (es)
DE (1)	DE69008591T3 (es)
DK (1)	DK0386826T3 (es)
ES (1)	ES2052157T5 (es)
NL (1)	NL8900539A (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
SE470131B (sv) *	1991-05-02	1993-11-15	Berol Nobel Ab	Förfarande för framställning av en amidinnehållande produktblandning, en amidinnehållande produktblandning samt dess användning
DE4216316A1 (de) *	1992-05-16	1993-11-18	Basf Ag	Tertiäre Amide und ihre Verwendung als schaumarme Netzmittel in der Textilindustrie
FR2693206B1 (fr) *	1992-07-02	1994-09-16	Oreal	Utilisation dans des solutions d'agents tensioactifs de carbamates d'aminopolyols en tant qu'épaississants et compositions les contenant.
DE4336247A1 (de) *	1993-10-22	1995-04-27	Basf Ag	Verwendung von endgruppenverschlossenen Fettsäureamidalkoxylaten
DE4409189C2 (de) *	1994-03-17	1996-08-14	Chem Y	Tensid-Zusammensetzung, insbesondere zur Verwendung in Körperreinigungsmitteln
ES2146268T3 (es) *	1994-06-27	2000-08-01	Kao Corp	Procedimiento para la fabricacion de acido amidoetercarboxilico o de una sal del mismo y de una mezcla de agentes con actividad superficial que los contienen.
WO1999019169A1 (en)	1997-10-14	1999-04-22	The Dow Chemical Company	Insulated heat sensitive component
EP1033363A1 (de) *	1999-03-02	2000-09-06	Goldschmidt Rewo GmbH & Co. KG	Verfahren zur Herstellung von Verdickungsmitteln auf Basis von Fettsäure-monoisopropanolamid, ihre Verwendung und diese enhaltende Zubereitungen
FR2833837B1 (fr) *	2001-12-21	2005-08-05	Oreal	Composition pour la teinture d'oxydation des fibres keratiniques comprenant un amide d'acide gras de colza oxyethylene
FR2940067B1 (fr) *	2008-12-19	2011-02-25	Oreal	Composition oxydante pour le traitement des fibres keratiniques comprenant un polymere cationique, un amide gras et un agent-oxygene
EP4453161A4 (en) *	2021-12-22	2026-01-21	Integrity Bio Chemicals Llc	COMPOSITIONS COMPRISING REACTION PRODUCTS OF SACCHARIDE POLYMERS AND FATTY ACIDS OR FATTY ESTERS FORMULATED WITH A NEUTRAL AMIDE-BASED SURFACTANT
EP4215518A1 (en) *	2022-01-24	2023-07-26	KAO CHEMICALS GmbH	Process for preparing amidated fatty acids and derivatives thereof

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB420545A (en) *	1932-02-29	1934-11-28	Ig Farbenindustrie Ag	Process for the manufacture of acid amide derivatives
DE1618397A1 (de) *	1967-04-01	1970-07-16	Hoechst Ag	Verfahren zur Herstellung farblich verbesserter und farbstabiler stickstoffhaltiger Fettsaeure-Kondensationsprodukte
AT335035B (de) *	1974-10-10	1977-02-25	Henkel & Cie Gmbh	Stabile suspensionen wasserunloslicher, zum binden von calciumionen befahigter silikate und deren verwendung zur herstellung von wasch- und reinigungsmitteln
US4169075A (en) *	1974-10-10	1979-09-25	Henkel Kommanditgesellschaft Auf Aktien	Process for the production of powdery washing agents by spray-drying
AT352241B (de) *	1977-04-22	1979-09-10	Henkel Kgaa	Pulverfoermiges, phosphatfreies textil- waschmittel
JPS5910760B2 (ja) *	1980-12-26	1984-03-10	ダスキンフランチヤイズ株式会社	粘性のある液体石鹸組成物
JPS6210197A (ja) *	1985-07-05	1987-01-19	日本油脂株式会社	非イオン性界面活性剤水溶液用粘度向上剤
JPS6210199A (ja) *	1985-07-05	1987-01-19	日本油脂株式会社	液状クレンザ−組成物
JPS6257495A (ja) *	1985-09-06	1987-03-13	日本油脂株式会社	ドライクリ−ニング用洗浄剤組成物
NL8502587A (nl) *	1985-09-20	1987-04-16	Chem Y	Werkwijze ter bereiding van oxyethyleengroepen en carboxymethylgroepen of zouten daarvan bevattende, capillairactieve produkten, alsmede de zo verkregen produkten en hun toepassing.

1989
- 1989-03-04 NL NL8900539A patent/NL8900539A/nl not_active Application Discontinuation
1990
- 1990-02-27 DK DK90200463.9T patent/DK0386826T3/da active
- 1990-02-27 DE DE69008591T patent/DE69008591T3/de not_active Expired - Lifetime
- 1990-02-27 AT AT9090200463T patent/ATE105280T1/de active
- 1990-02-27 ES ES90200463T patent/ES2052157T5/es not_active Expired - Lifetime
- 1990-02-27 EP EP90200463A patent/EP0386826B2/en not_active Expired - Lifetime
- 1990-03-01 US US07/485,873 patent/US5124079A/en not_active Expired - Lifetime
- 1990-09-28 DD DD90344288A patent/DD295342A5/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
DK0386826T3 (da)	1994-06-06
EP0386826B2 (en)	1997-11-05
ES2052157T3 (es)	1994-07-01
ATE105280T1 (de)	1994-05-15
DE69008591D1 (de)	1994-06-09
ES2052157T5 (es)	1997-12-16
DE69008591T2 (de)	1994-09-22
EP0386826B1 (en)	1994-05-04
EP0386826A1 (en)	1990-09-12
US5124079A (en)	1992-06-23
DE69008591T3 (de)	1998-04-02
NL8900539A (nl)	1990-10-01

Legal Events

Date	Code	Title
1994-03-17	RPI	Change in the person, name or address of the patentee (searches according to art. 11 and 12 extension act)
1994-05-05	RPV	Change in the person, the name or the address of the representative (searches according to art. 11 and 12 extension act)
1998-07-16	ENJ	Ceased due to non-payment of renewal fee

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DE69805528T2 (de)	2002-10-31	Haarpflegemittel und 2 in 1 pflegeshampoo
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EP0243619B1 (de)	1991-03-20	Verfahren zur Herstellung einer hochkonzentrierten, fliess- und pumpfähigen Betainlösung
DE69105870T2 (de)	1995-05-24	Kationische Verbindung und Reinigungsmittelzusammensetzung.
DE3826654C1 (es)	1991-01-31
EP2854950A2 (de)	2015-04-08	Verwendung von n-methyl-n-acylglucaminen als kältestabilisatoren in tensidlösungen
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DE69913934T2 (de)	2004-11-04	Zusammensetzung enthaltend eine Mischung von Glycerin und alkoxylierten Mono-, Di- und Triglyceride
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DE69527272T2 (de)	2003-03-06	Reinigungszusammensetzung
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DE69416524T2 (de)	1999-06-10	Hautreinigungstück
EP0647613B1 (de)	1998-01-14	Verfahren zur Herstellung hochkonzentrierter fliessfähiger wässriger Lösungen von Betainen
DE69932706T2 (de)	2007-08-02	Verbesserte alkanolamide
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