EP1678239A1 - Amino-functional silicone waxes - Google Patents

Amino-functional silicone waxes

Info

Publication number
EP1678239A1
EP1678239A1 EP04769548A EP04769548A EP1678239A1 EP 1678239 A1 EP1678239 A1 EP 1678239A1 EP 04769548 A EP04769548 A EP 04769548A EP 04769548 A EP04769548 A EP 04769548A EP 1678239 A1 EP1678239 A1 EP 1678239A1
Authority
EP
European Patent Office
Prior art keywords
waxes
formula
silicone waxes
silicone
amino
Prior art date
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.)
Withdrawn
Application number
EP04769548A
Other languages
German (de)
French (fr)
Inventor
Bernard Danner
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Clariant Finance BVI Ltd
Original Assignee
Clariant International Ltd
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.)
Filing date
Publication date
Application filed by Clariant International Ltd filed Critical Clariant International Ltd
Priority to EP04769548A priority Critical patent/EP1678239A1/en
Publication of EP1678239A1 publication Critical patent/EP1678239A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • C08L83/04—Polysiloxanes
    • C08L83/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/38—Polysiloxanes modified by chemical after-treatment
    • C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
    • C08G77/388—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing nitrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • C08L83/04—Polysiloxanes
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • D06M15/6436—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing amino groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/045—Polysiloxanes containing less than 25 silicon atoms
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
    • C08G77/18—Polysiloxanes containing silicon bound to oxygen-containing groups to alkoxy or aryloxy groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
    • C08G77/24—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen halogen-containing groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
    • C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
    • C08G77/28—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen sulfur-containing groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/42—Block-or graft-polymers containing polysiloxane sequences
    • C08G77/452—Block-or graft-polymers containing polysiloxane sequences containing nitrogen-containing sequences
    • C08G77/455—Block-or graft-polymers containing polysiloxane sequences containing nitrogen-containing sequences containing polyamide, polyesteramide or polyimide sequences
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/50—Modified hand or grip properties; Softening compositions

Definitions

  • the present invention concerns silicone waxes having plural tertiary or quaternary amino groups, their preparation and their use as softeners in the textile industry.
  • the invention accordingly provides amino-functional silicone waxes of the formulae (I) to (IV)
  • R is Cn-C 22 -alkyl, linear or branched
  • R1 is C C 7 -alkyl or benzyl, preferably methyl or benzyl,
  • R2 is -OH, -CH 3> -OCH 3 , -OC 2 H 5 ,
  • a " is CH 3 OSO 3 " , chloride, bromide, iodide or tosylsulfate, preferably CH 3 OSO 3 " or chloride, n is 2 or 3, p is 10-200, preferably 20-50, q+z is 10-400, preferably 15-200, and q/z is 5-50, preferably 10-30.
  • waxes whether in the quaternized form (II) and (IV) or in the non-quaternized form (I) and (III), exhibit good properties when used as softeners. Their great advantage is that they can be used in the form of dispersions which, compared with emulsions, have a higher shearing force stability.
  • the present invention further provides for the preparation of the aforementioned silicone waxes.
  • the initial step is to prepare fatty acid diamides by condensation of fatty acids, for example stearic acid or lauric acid, with diethylenetriamine or dipropylenediamine.
  • the resultant fatty acid diamide is subsequently quaternized with the customary, aforementioned quaternizing agents.
  • the present invention further provides for the use of the aforementioned silicone waxes as softeners in the textile industry.
  • the silicone waxes obtained can be converted by means of dispersants into aqueous dispersions which have a higher shearing force stability than emulsions and are very useful for softening textiles in that the material acquires a pleasant, soft hand.
  • the waxes have the following structure:
  • n 2 or 3
  • R C ⁇ -C ⁇ alkyl radical
  • n 2 or 3
  • R C 11 -C 21 alkyl radical are obtained.
  • the products W E to W 12 -E and also WQ E to WQ 12 -E are very stable to shearing force; they can be applied to textile material (cotton and synthetic fibres) both in the padding process and in the exhaust process.
  • the finished textile materials possess an excellent, soft, pleasant, smooth hand.
  • the finished substrate is added to an aqueous liquor which, based on the substrate, contains 0.5% to 4.0% of the end products described in the examples, at about 40°C and a liquor ratio of 6:1 to 20:1 , in a laboratory jet. After 20 minutes at pH 5.0 to 6.0 (40°C) and continuous agitation of the substrate, the substrate is removed from the liquor, whizzed and dried tensionlessly at 140°C for 70-90 seconds.
  • the finished substrate is padded at room temperature, to a 100% dry weight increase, with an aqueous liquor which contains 15 to 60 g/l of the end products W-E or WQ-E.
  • the padded material is subsequently dried at 140°C for 70-90 seconds.
  • Substrate Exhaust process: Tricot fabric, dyed, with or without setting - 100% cotton - polyester (50%) / cotton (50%)
  • Padding process Tricot or woven fabric, dyed, with or without setting - 100% cotton - polyester (50%) / cotton (50%) - polyester (100%) - polyacrylonitrile (100%) - nylon 6 (100%)
  • Softness can be tested pairwise or using a handle-O-meter (for example a 211-5 Twing Albert).
  • the finished samples are first conditioned (24 hours, 20°C, 65% relative humidity) before being assessed.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Silicon Polymers (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The present invention relates to silicone waxes having plural tertiary or quaternary amino groups, their preparation and their use as softeners in the textile industry. These waxes can be processed into stable aqueous dispersions and lead to products having a pleasant, soft hand.

Description

AMINO-FUNCTIONAL SILICONE WAXES
The present invention concerns silicone waxes having plural tertiary or quaternary amino groups, their preparation and their use as softeners in the textile industry.
There is extensive literature on amino-functional silicone compounds. These compounds are used for example as plasticizers in the textile industry, as surface- treating agents, as thickeners or in the cosmetic industry. Nonetheless, there is a demand in the textile industry for softening substances which lead to products having a superior hand and which do not have the disadvantage of unstable emulsions in use.
It has now been found that certain silicone waxes having plural tertiary or quaternary nitrogen atoms can be processed into stable aqueous dispersions and have surprisingly good properties when used as softeners in the textile industry and lead to products having a pleasant, soft hand.
The invention accordingly provides amino-functional silicone waxes of the formulae (I) to (IV)
where
R is Cn-C22-alkyl, linear or branched,
R1 is C C7-alkyl or benzyl, preferably methyl or benzyl,
R2 is -OH, -CH3> -OCH3, -OC2H5,
A" is CH3OSO3 ", chloride, bromide, iodide or tosylsulfate, preferably CH3OSO3 " or chloride, n is 2 or 3, p is 10-200, preferably 20-50, q+z is 10-400, preferably 15-200, and q/z is 5-50, preferably 10-30.
These waxes, whether in the quaternized form (II) and (IV) or in the non-quaternized form (I) and (III), exhibit good properties when used as softeners. Their great advantage is that they can be used in the form of dispersions which, compared with emulsions, have a higher shearing force stability.
The present invention further provides for the preparation of the aforementioned silicone waxes. The initial step is to prepare fatty acid diamides by condensation of fatty acids, for example stearic acid or lauric acid, with diethylenetriamine or dipropylenediamine.
The resultant fatty acid diamide is reacted with silicone oils of the general formula (V)
where p has the same meaning as in formula (I) or (II), to prepare the waxes of formula (I) or (II),
or subsequently quaternized with the customary quaternizing agents such as methyl sulfate, ethyl sulfate, methyl halide, benzyl chloride or tosyl sulfate to prepare the waxes of the formula (II). The starting materials and their preparation will be known to one skilled in the art.
To prepare the waxes of the formula (III) or (IV), the resultant fatty acid diamide is reacted with silicone oils of the general formula (VI)
where R2, (q+z) and q/z have the same meaning as in formula (III) or (IV),
and to prepare the waxes of the formula (IV), the resultant fatty acid diamide is subsequently quaternized with the customary, aforementioned quaternizing agents.
The present invention further provides for the use of the aforementioned silicone waxes as softeners in the textile industry. The silicone waxes obtained can be converted by means of dispersants into aqueous dispersions which have a higher shearing force stability than emulsions and are very useful for softening textiles in that the material acquires a pleasant, soft hand.
EXAMPLES 1. Preparation of fatty acid diamides (Fatty acid: RCOOH)
1.1 Preparation of R-CONH(CH2)2NH(CH2)2NHCO-R 2 mol of fatty acid are heated to 105°C under nitrogen; 1 mol of diethylenetri- amine is then added dropwise while at the same time the temperature is raised to 130°C. This is followed by 24 hours of condensation at 130°C under a slow stream of nitrogen using a distillation bridge. The reaction mixture is subsequently discharged. The acid number of the reaction mixture (number of mg of KOH to neutralize 1 g of product) is less than 7. The resultant amount of condensation product requires less than 1.1 mol of perchloric acid to titrate the free amino groups.
1.2 Preparation of R-CONH(CH2)3NH(CH2)3NHCO-R 1.1 is repeated using dipropylenediamine instead of diethylenediamine.
2. Preparation of silicone waxes 2.1 Silicone waxes W. - W6 661.5 parts of the silicone oil of the formula
are reacted at 150°C under nitrogen for 14 hours with x parts of the diamides D-i to D6. A check is subsequently carried out to see that glycidyl groups are no longer present. The following waxes are obtained:
The waxes have the following structure:
2.2 Silicone waxes W7 - W12 661.5 parts of the silicone oil of the formula
are reacted at 150°C under nitrogen for 14 hours with x parts of the diamides D^ to D6. A check is subsequently carried out to see that glycidyl groups have reacted quantitatively. The following waxes are obtained:
The waxes have the following structure: n = 2 or 3, R = C^-C^ alkyl radical
Preparation of quaternized silicone waxes WQi - WQ 2 x parts of silicone wax W are melted and allowed to react with 25.2 parts of dimethyl sulfate for 2 hours at about 70-75°C.
Waxes having the structures: and
n = 2 or 3, R = C11-C21 alkyl radical are obtained.
4. Preparation of end products 4.1 Based on silicone waxes \N^ - W12 125.0 parts of silicone wax (W) are melted. 25.0 parts of a 70% solution of
CH, C17H35CONH(CH2)3— N-CH3 ? CH3OS03 Θ CH,
(dispersant 1 ) in propylene glycol and also 37.5 parts of stearyl poly-10-glycol ether (dispersant 2) are then added. As soon as there is a homogeneous melt, 800.0 parts of water are added in increments with stirring. Finally, 12.5 parts of glacial acetic acid are added. This gives 1000.0 parts of a 12.5% silicone wax dispersion (W-E). 4.2 Based on quaternary silicone waxes WQi - WQ12 4.1 is repeated except that the silicone waxes (WQ) are used instead of the silicone waxes (W) and 12.5 parts of water are added at the end instead of 12.5 parts of glacial acetic acid. This gives 1000.0 parts of a 12.5% silicone wax dispersion (WQ-E).
The products W E to W12-E and also WQ E to WQ12-E are very stable to shearing force; they can be applied to textile material (cotton and synthetic fibres) both in the padding process and in the exhaust process. The finished textile materials possess an excellent, soft, pleasant, smooth hand.
APPLICATION EXAMPLES The following finishing operations were carried out:
• Exhaust process The finished substrate is added to an aqueous liquor which, based on the substrate, contains 0.5% to 4.0% of the end products described in the examples, at about 40°C and a liquor ratio of 6:1 to 20:1 , in a laboratory jet. After 20 minutes at pH 5.0 to 6.0 (40°C) and continuous agitation of the substrate, the substrate is removed from the liquor, whizzed and dried tensionlessly at 140°C for 70-90 seconds.
• Padding process The finished substrate is padded at room temperature, to a 100% dry weight increase, with an aqueous liquor which contains 15 to 60 g/l of the end products W-E or WQ-E. The padded material is subsequently dried at 140°C for 70-90 seconds.
Substrate: Exhaust process: Tricot fabric, dyed, with or without setting - 100% cotton - polyester (50%) / cotton (50%) Padding process: Tricot or woven fabric, dyed, with or without setting - 100% cotton - polyester (50%) / cotton (50%) - polyester (100%) - polyacrylonitrile (100%) - nylon 6 (100%)
Testing: Softness can be tested pairwise or using a handle-O-meter (for example a 211-5 Twing Albert). The finished samples are first conditioned (24 hours, 20°C, 65% relative humidity) before being assessed.
All the finishes show a distinct improvement in softness compared with unfinished fabric.

Claims

1. Amino-functional silicone waxes of the formulae (I) to (IV)
where
R is Cn-C22-alkyl, linear or branched,
R1 is CτC7-alkyl or benzyl,
R2 is -OH, -CH3> -OCH3> -OC2H5,
A" is CH3OSO3 ", chloride, bromide, iodide or tosylsulfate, n is 2 or 3, p is 10-200, q+z is 10-400, and q/z is 5-50.
Amino-functional silicone waxes according to Claim 1 wherein
R, R2 and n are each as defined above,
R1 is methyl or benzyl,
A" is CH3OSO3 " or chloride, p is 20-50, q+z is 15-200, and q/z is 10-30.
Process for preparating amino-functional silicone waxes of the formulae (I) or (III) according to Claim 1, characterized in that fatty acid diamides are prepared by condensation of fatty acids with diethylenetriamine or dipropylenediamine and then reacted with silicone oils of the general formula (V)
where p has the same meaning as in formula (I) or (II), to prepare the waxes of the formula (I)
or with silicone oils of the formula (VI) 13
where R2, (q+z) and q/z have the same meaning as in formula (III) or (IV), to prepare the waxes of the formula (III).
Process according to Claim 3, characterized in that the resultant silicone waxes of the formula (I) or (III) are quaternized to the compounds of the formulae (II) or (IV).
Process according to Claim 3 or 4, characterized in that the fatty acids are stearic acid, behenic acid or lauric acid.
6. Use of the silicone waxes according to Claims 1 or 2 as softeners in the textile industry.
7. Use according to Claim 7, characterized in that the silicone waxes are used in the form of aqueous dispersions.
EP04769548A 2003-10-07 2004-10-04 Amino-functional silicone waxes Withdrawn EP1678239A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP04769548A EP1678239A1 (en) 2003-10-07 2004-10-04 Amino-functional silicone waxes

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP03022447 2003-10-07
EP04769548A EP1678239A1 (en) 2003-10-07 2004-10-04 Amino-functional silicone waxes
PCT/IB2004/003227 WO2005035631A1 (en) 2003-10-07 2004-10-04 Amino-functional silicone waxes

Publications (1)

Publication Number Publication Date
EP1678239A1 true EP1678239A1 (en) 2006-07-12

Family

ID=34429232

Family Applications (1)

Application Number Title Priority Date Filing Date
EP04769548A Withdrawn EP1678239A1 (en) 2003-10-07 2004-10-04 Amino-functional silicone waxes

Country Status (5)

Country Link
EP (1) EP1678239A1 (en)
CN (1) CN100384913C (en)
BR (1) BRPI0415170A (en)
HK (1) HK1095846A1 (en)
WO (1) WO2005035631A1 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102008001867A1 (en) * 2008-05-19 2009-11-26 Wacker Chemie Ag Process for the preparation of quaternary ammonium organopolysiloxanes
EP2658638B1 (en) 2010-12-28 2014-09-03 Unilever N.V. Method for production of an emulsion
DE102012213248A1 (en) * 2012-07-27 2014-01-30 Henkel Ag & Co. Kgaa Nourishing hair dye with silicone (s) and polymer (s)
JP6633551B2 (en) * 2014-06-12 2020-01-22 ザ ケマーズ カンパニー エフシー リミテッド ライアビリティ カンパニー Wax and urethane based extender blends for surface effect compositions

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8919669D0 (en) * 1989-08-31 1989-10-11 Unilever Plc Fabric-softening compositions
FR2733245B1 (en) * 1995-04-18 1997-05-23 Rhone Poulenc Chimie USE OF SILICON WAXES WITH ESTER FUNCTIONS TO THICKEN OILY MEDIA
FR2739284B1 (en) * 1995-09-29 1997-11-07 Oreal COMPOSITION FOR THE TREATMENT OF KERATINIC MATERIALS COMPRISING AT LEAST ONE GRAFTED SILICONE POLYMER AND AT LEAST ONE FATTY CHAIN AMIDE AND USES THEREOF
FR2749505B1 (en) * 1996-06-07 1998-07-10 Oreal ALKYLPOLYSILOXANE NON-TRANSFER MAKEUP OR CARE COMPOSITION

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2005035631A1 *

Also Published As

Publication number Publication date
BRPI0415170A (en) 2006-11-28
WO2005035631A1 (en) 2005-04-21
CN1863844A (en) 2006-11-15
HK1095846A1 (en) 2007-05-18
CN100384913C (en) 2008-04-30

Similar Documents

Publication Publication Date Title
JP5553505B2 (en) Polyamino and / or polyammonium / polysiloxane copolymer compound in which polyalkylene oxide units are arranged in a comb shape
EP0342834B1 (en) Treatment of fibrous materials
US4818242A (en) Laundry care product for final rinse: aqueous mixture of cationic silicone oil, cationic fatty acid condensate and cationic film-former
US5098979A (en) Novel silicone quaternary compounds
US5352817A (en) Cationic silicones
CA2024797C (en) Microemulsions of aminopolysiloxanes
AU726675B2 (en) Silicone aminopolyalkyleneoxide block copolymers
US5153294A (en) Silicone ester quaternary compounds
US5166297A (en) Silicone ester quaternary compounds
RU2141015C1 (en) Composition for imparting to textile material of fire- retarding and cloth-softening properties, textile material and method of composition production
CN109535428B (en) Polyammonium modified polyether silicone oil and preparation method and application thereof
US5115049A (en) Fatty carboxylic silicone amine salts
US5496401A (en) Aqueous emulsion containing an oxidatively crosslinked aminopolysiloxane
JPH07166064A (en) Organosilicon composition for treating fiber product
EP1678239A1 (en) Amino-functional silicone waxes
US7511165B2 (en) Amino-functional silicone waxes
JPH02277888A (en) Treating fibrous fabric and other base material with absorptive cationic silicone
JPS6328417B2 (en)
WO2004047779A2 (en) Polymers containing quaternary ammonium salts
KR0134183B1 (en) Micro-emulsion of aminopolysiloxans
US5080811A (en) Ethoxylated fatty acid amide textile softeners
JP2009513742A (en) Polyorganosiloxane
US20040024112A1 (en) Stable aqueous polymer emulsions, production and use thereof
JP2003003369A (en) Softening base agent and softening and finishing agent
WO2002031256A1 (en) Polysiloxanes with quaternary groups featuring nitrogen atoms

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20060508

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LI LU MC NL PL PT RO SE SI SK TR

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: CLARIANT FINANCE (BVI) LIMITED

DAX Request for extension of the european patent (deleted)
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN WITHDRAWN

18W Application withdrawn

Effective date: 20090624