ZA200502599B - Alkyl glycidol carbonates used as co-surfactants - Google Patents

Alkyl glycidol carbonates used as co-surfactants Download PDF

Info

Publication number: ZA200502599B
Authority: ZA; South Africa
Prior art keywords: compounds; linear; formula; branched; cleaner
Prior art date: 2002-10-01

Application number

ZA200502599A

Other languages

English (en)

Inventor

Ralf Noerenberg

Christian Wulff

Juergen Tropsch

Martin Scholtissek

Michael Kluge

Original Assignee

Basf 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.)

2002-10-01

Filing date

2005-03-31

Publication date

2006-06-28

2005-03-31 Application filed by Basf Ag filed Critical Basf Ag

2006-06-28 Publication of ZA200502599B publication Critical patent/ZA200502599B/en

Links

-1 Alkyl glycidol carbonates Chemical class 0.000 title claims description 37
239000004094 surface-active agent Substances 0.000 title description 17
239000000203 mixture Substances 0.000 claims description 60
150000001875 compounds Chemical class 0.000 claims description 39
150000001298 alcohols Chemical class 0.000 claims description 36
239000004064 cosurfactant Substances 0.000 claims description 32
125000000217 alkyl group Chemical group 0.000 claims description 22
239000003599 detergent Substances 0.000 claims description 22
150000002924 oxiranes Chemical class 0.000 claims description 20
229910052739 hydrogen Inorganic materials 0.000 claims description 18
239000001257 hydrogen Substances 0.000 claims description 18
150000001412 amines Chemical class 0.000 claims description 15
238000006243 chemical reaction Methods 0.000 claims description 15
238000009472 formulation Methods 0.000 claims description 12
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 11
150000004649 carbonic acid derivatives Chemical class 0.000 claims description 10
239000000499 gel Substances 0.000 claims description 10
150000001735 carboxylic acids Chemical class 0.000 claims description 9
125000002947 alkylene group Chemical group 0.000 claims description 8
150000003857 carboxamides Chemical class 0.000 claims description 8
239000007788 liquid Substances 0.000 claims description 8
238000000034 method Methods 0.000 claims description 8
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims description 7
150000002431 hydrogen Chemical class 0.000 claims description 7
150000003573 thiols Chemical class 0.000 claims description 7
125000004432 carbon atom Chemical group C* 0.000 claims description 6
238000004519 manufacturing process Methods 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 5
239000003054 catalyst Substances 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
125000001424 substituent group Chemical group 0.000 claims description 5
150000000180 1,2-diols Chemical class 0.000 claims description 4
125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 4
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239000006260 foam Substances 0.000 claims description 4
239000007787 solid Substances 0.000 claims description 4
125000001931 aliphatic group Chemical group 0.000 claims description 3
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150000001340 alkali metals Chemical class 0.000 description 3
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239000008139 complexing agent Substances 0.000 description 3
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 3
230000001804 emulsifying effect Effects 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
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239000001205 polyphosphate Substances 0.000 description 3
235000011176 polyphosphates Nutrition 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
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BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
XMVBHZBLHNOQON-UHFFFAOYSA-N 2-butyl-1-octanol Chemical compound CCCCCCC(CO)CCCC XMVBHZBLHNOQON-UHFFFAOYSA-N 0.000 description 2
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
230000002776 aggregation Effects 0.000 description 2
238000004220 aggregation Methods 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
150000001342 alkaline earth metals Chemical class 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
239000002280 amphoteric surfactant Substances 0.000 description 2
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229910052799 carbon Inorganic materials 0.000 description 2
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239000003093 cationic surfactant Substances 0.000 description 2
150000001768 cations Chemical class 0.000 description 2
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
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150000002191 fatty alcohols Chemical class 0.000 description 2
238000007306 functionalization reaction Methods 0.000 description 2
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239000003112 inhibitor Substances 0.000 description 2
UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 description 2
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239000003906 humectant Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical class C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
239000000976 ink Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
238000003780 insertion Methods 0.000 description 1
230000037431 insertion Effects 0.000 description 1
238000005342 ion exchange Methods 0.000 description 1
239000002563 ionic surfactant Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000010985 leather Substances 0.000 description 1
150000007527 lewis bases Chemical class 0.000 description 1
235000019421 lipase Nutrition 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
239000004530 micro-emulsion Substances 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000000178 monomer Substances 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
239000004745 nonwoven fabric Substances 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
239000003973 paint Substances 0.000 description 1
HWGNBUXHKFFFIH-UHFFFAOYSA-I pentasodium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O HWGNBUXHKFFFIH-UHFFFAOYSA-I 0.000 description 1
238000010587 phase diagram Methods 0.000 description 1
150000003009 phosphonic acids Chemical class 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
229910052615 phyllosilicate Inorganic materials 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920001983 poloxamer Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920006254 polymer film Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
239000011591 potassium Substances 0.000 description 1
238000007639 printing Methods 0.000 description 1
230000008569 process Effects 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000007670 refining Methods 0.000 description 1
238000000518 rheometry Methods 0.000 description 1
150000003333 secondary alcohols Chemical class 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
235000019795 sodium metasilicate Nutrition 0.000 description 1
URLJMZWTXZTZRR-UHFFFAOYSA-N sodium myristyl sulfate Chemical compound CCCCCCCCCCCCCCOS(O)(=O)=O URLJMZWTXZTZRR-UHFFFAOYSA-N 0.000 description 1
229950005425 sodium myristyl sulfate Drugs 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 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
MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
239000002689 soil Substances 0.000 description 1
230000003381 solubilizing effect Effects 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
235000000346 sugar Nutrition 0.000 description 1
150000008163 sugars Chemical class 0.000 description 1
230000001180 sulfating effect Effects 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
239000012209 synthetic fiber Substances 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
239000007885 tablet disintegrant Substances 0.000 description 1
239000003760 tallow Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
FRPJTGXMTIIFIT-UHFFFAOYSA-N tetraacetylethylenediamine Chemical compound CC(=O)C(N)(C(C)=O)C(N)(C(C)=O)C(C)=O FRPJTGXMTIIFIT-UHFFFAOYSA-N 0.000 description 1
238000012546 transfer Methods 0.000 description 1
230000009466 transformation Effects 0.000 description 1
230000007704 transition Effects 0.000 description 1
239000001226 triphosphate Substances 0.000 description 1
KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 1
238000010792 warming Methods 0.000 description 1
238000005406 washing Methods 0.000 description 1
210000002268 wool Anatomy 0.000 description 1
239000002888 zwitterionic surfactant Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/32—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D317/34—Oxygen atoms
- C07D317/36—Alkylene carbonates; Substituted alkylene carbonates
- C07D317/38—Ethylene carbonate
- 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
- C11D1/38—Cationic compounds
- C11D1/42—Amino alcohols or amino ethers
- 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
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/528—Carboxylic amides (R1-CO-NR2R3), where at least one of the chains R1, R2 or R3 is interrupted by a functional group, e.g. a -NH-, -NR-, -CO-, or -CON- group
- 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
- C11D1/66—Non-ionic compounds
- 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
- C11D1/66—Non-ionic compounds
- C11D1/667—Neutral esters, e.g. sorbitan esters
- 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
- C11D3/20—Organic compounds containing oxygen
- C11D3/2096—Heterocyclic compounds
- 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
- 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
- C11D3/34—Organic compounds containing sulfur
- C11D3/3427—Organic compounds containing sulfur containing thiol, mercapto or sulfide groups, e.g. thioethers or mercaptales

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Wood Science & Technology (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Emergency Medicine (AREA)
Detergent Compositions (AREA)
Cosmetics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

ZA200502599A 2002-10-01 2005-03-31 Alkyl glycidol carbonates used as co-surfactants ZA200502599B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE10246139A DE10246139A1 (de)	2002-10-01	2002-10-01	Alkylglycidolcarbonate als Co-Tenside

Publications (1)

Publication Number	Publication Date
ZA200502599B true ZA200502599B (en)	2006-06-28

Family

ID=32010144

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200502599A ZA200502599B (en)	2002-10-01	2005-03-31	Alkyl glycidol carbonates used as co-surfactants

Country Status (13)

Country	Link
US (1)	US20060009368A1 (ja)
EP (1)	EP1549631B1 (ja)
JP (1)	JP4778232B2 (ja)
KR (1)	KR20050053728A (ja)
CN (1)	CN100420684C (ja)
AU (1)	AU2003277923A1 (ja)
BR (1)	BR0314939A (ja)
CA (1)	CA2500780A1 (ja)
DE (1)	DE10246139A1 (ja)
MX (1)	MXPA05003110A (ja)
PL (1)	PL376539A1 (ja)
WO (1)	WO2004031167A1 (ja)
ZA (1)	ZA200502599B (ja)

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DE102007016382A1 (de) *	2007-04-03	2008-10-09	Henkel Ag & Co. Kgaa	Vergrauungsinhibierendes Waschmittel
DE102007016389A1 (de) *	2007-04-03	2008-10-09	Henkel Ag & Co. Kgaa	Mittel zur Behandlung harter Oberflächen
DE102007016383A1 (de) *	2007-04-03	2008-10-09	Henkel Ag & Co. Kgaa	Fixierung von Duftstoffen aus Wasch- und Reinigungsmitteln an harten und weichen Oberflächen
EA017884B1 (ru) *	2008-03-25	2013-03-29	Зингента Партисипейшнс Аг	Композиции поверхностно-активных веществ
EA023144B1 (ru) *	2011-04-13	2016-04-29	Басф Се	Аминные и диаминные соединения и их применение для обратной пенной флотации силиката из железной руды
CN104768523B (zh)	2012-10-29	2017-08-15	宝洁公司	10℃下具有0.30或更大损耗角正切值的个人护理组合物
WO2017085152A1 (en) *	2015-11-16	2017-05-26	Firmenich Sa	Odor neutralizer for ammonia and primary or secondary amines
EP3873623A1 (en) *	2018-11-02	2021-09-08	Johnson & Johnson Consumer Inc.	Foamable solid cleanser

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DE19543162A1 (de) *	1995-11-18	1997-05-22	Basf Ag	Feste Textilwaschmittel-Formulierung aus anorganischen Buildern, Glycin-N,N-diessigsäure-Derivaten als organische Cobuilder sowie anionischen und nichtionischen Tensiden
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FR2800383B1 (fr)	1999-10-29	2002-01-18	Rhodia Chimie Sa	Complexe silicone/adhesif anti-adherent avec additif de stabilisation dans silicone
KR100371403B1 (ko)	2000-01-10	2003-02-07	주식회사 엘지화학	새로운 전해액과 이를 이용한 리튬이온 전지
JP2001300286A (ja) *	2000-04-20	2001-10-30	Lion Corp	分解性界面活性剤
DE10035617A1 (de)	2000-07-21	2002-01-31	Basf Ag	Sekundäre C¶1¶¶0¶-C¶1¶¶8¶-Tensidalkohole

2002
- 2002-10-01 DE DE10246139A patent/DE10246139A1/de not_active Withdrawn
2003
- 2003-09-30 PL PL376539A patent/PL376539A1/pl not_active Application Discontinuation
- 2003-09-30 AU AU2003277923A patent/AU2003277923A1/en not_active Abandoned
- 2003-09-30 US US10/528,700 patent/US20060009368A1/en not_active Abandoned
- 2003-09-30 JP JP2004540753A patent/JP4778232B2/ja not_active Expired - Fee Related
- 2003-09-30 CN CNB038236508A patent/CN100420684C/zh not_active Expired - Fee Related
- 2003-09-30 EP EP03769344.7A patent/EP1549631B1/de not_active Expired - Lifetime
- 2003-09-30 BR BR0314939-0A patent/BR0314939A/pt not_active Application Discontinuation
- 2003-09-30 WO PCT/EP2003/010841 patent/WO2004031167A1/de active Application Filing
- 2003-09-30 CA CA002500780A patent/CA2500780A1/en not_active Abandoned
- 2003-09-30 KR KR1020057005726A patent/KR20050053728A/ko not_active Application Discontinuation
- 2003-09-30 MX MXPA05003110A patent/MXPA05003110A/es unknown
2005
- 2005-03-31 ZA ZA200502599A patent/ZA200502599B/en unknown

Also Published As

Publication number	Publication date
CN100420684C (zh)	2008-09-24
DE10246139A1 (de)	2004-04-15
MXPA05003110A (es)	2005-06-22
EP1549631A1 (de)	2005-07-06
JP4778232B2 (ja)	2011-09-21
PL376539A1 (pl)	2006-01-09
AU2003277923A1 (en)	2004-04-23
WO2004031167A1 (de)	2004-04-15
KR20050053728A (ko)	2005-06-08
JP2006504708A (ja)	2006-02-09
US20060009368A1 (en)	2006-01-12
EP1549631B1 (de)	2014-01-08
CN1688567A (zh)	2005-10-26
CA2500780A1 (en)	2004-04-15
BR0314939A (pt)	2005-08-02

Publication	Publication Date	Title
ZA200502599B (en)	2006-06-28	Alkyl glycidol carbonates used as co-surfactants
EP1235820B1 (en)	2006-08-23	Ether-capped poly(oxyalkylated) alcohol surfactants
US5945393A (en)	1999-08-31	Nonionic gemini surfactants
CA2391988A1 (en)	2001-06-14	Compositions including ether-capped poly(oxyalkylated) alcohol surfactants
JP2006104438A (ja)	2006-04-20	陰イオン界面活性剤を含む組成物
WO2000050549A2 (en)	2000-08-31	Cleaning compositions containing selected nonionic surfactants
ZA200502597B (en)	2006-06-28	Reaction products of 2-propylheptanol with 1-halogen-2,3-epoxypropanes and 1-hydroxy-2,3-epoxypropane
US20050256313A1 (en)	2005-11-17	Co-surfactants based on aldehydes
US5811384A (en)	1998-09-22	Nonionic gemini surfactants
CA2391995A1 (en)	2001-06-14	Ether-capped poly(oxyalkylated) alcohol surfactants
JP2013504525A (ja)	2013-02-07	イソソルビドグリセリルエーテル誘導体およびそれらの家庭用用途における使用
EP2295030A1 (en)	2011-03-16	Use of isosorbide ethers in detergents and cleaners
Bognolo	2018	Nonionic surfactants
EP2336281A1 (en)	2011-06-22	Use of anionic isosorbide derivatives (III)
KR100803898B1 (ko)	2008-02-15	아민옥사이드계 계면활성제 및 이를 이용한 세정제 조성물
WO2004065373A1 (de)	2004-08-05	Co-tenside mit ungesättigten heterocyclischen kopfgruppen