JPH07505189A - Concentrated fabric softening composition - Google Patents

Concentrated fabric softening composition

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Publication number
JPH07505189A
JPH07505189A JP5506335A JP50633593A JPH07505189A JP H07505189 A JPH07505189 A JP H07505189A JP 5506335 A JP5506335 A JP 5506335A JP 50633593 A JP50633593 A JP 50633593A JP H07505189 A JPH07505189 A JP H07505189A
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acid
composition
ester
chelating agent
fabric softening
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ドメイエール,ユーゴ ジャン マリー
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ザ、プロクター、エンド、ギャンブル、カンパニー
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/46Compounds containing quaternary nitrogen atoms
    • D06M13/461Quaternised amin-amides from polyamines or heterocyclic compounds or polyamino-acids
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/58Heterocyclic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/001Softening compositions
    • C11D3/0015Softening compositions liquid
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2075Carboxylic acids-salts thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2075Carboxylic acids-salts thereof
    • C11D3/2086Hydroxy carboxylic acids-salts thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/33Amino carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/36Organic compounds containing phosphorus
    • C11D3/364Organic compounds containing phosphorus containing nitrogen
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/224Esters of carboxylic acids; Esters of carbonic acid
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/35Heterocyclic compounds
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/35Heterocyclic compounds
    • D06M13/352Heterocyclic compounds having five-membered heterocyclic rings
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/35Heterocyclic compounds
    • D06M13/355Heterocyclic compounds having six-membered heterocyclic rings
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/46Compounds containing quaternary nitrogen atoms
    • D06M13/463Compounds containing quaternary nitrogen atoms derived from monoamines
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/46Compounds containing quaternary nitrogen atoms
    • D06M13/47Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds
    • D06M13/473Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds having five-membered heterocyclic rings
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/50Modified hand or grip properties; Softening compositions

Abstract

(57)【要約】本公報は電子出願前の出願データであるため要約のデータは記録されません。 (57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 濃縮布帛柔軟化組成物 技 術 分 野 本発明は、洗濯サイクルのすすぎ工程で使用すべき液体形の濃縮布帛柔軟化組成 物に関する。[Detailed description of the invention] Concentrated fabric softening composition Technical field The present invention provides concentrated fabric softening compositions in liquid form for use in the rinse step of a laundry cycle. relating to things.

背 景 技 術 洗濯サイクルのすすぎ工程で添加すべき布帛柔軟化組成物は、技術上周知であり 且つ大規模な商業的な応用を見出してきた。Background technique Fabric softening compositions to be added in the rinse step of a laundry cycle are well known in the art. and has found large-scale commercial applications.

優秀な布帛柔軟化性能を達成することに加えて、近年、布帛柔軟剤製造業者の目 的は、向上した生分解性を有する組成物を提供することになってきた。In addition to achieving excellent fabric softening performance, in recent years fabric softener manufacturers have The aim has been to provide compositions with improved biodegradability.

従って、エステル含有布帛柔軟化活性成分は、通常の第四級柔軟化活性成分の代 替品または通常の第四級柔軟化活性成分との組み合わせで使用すべきことが開示 されている。このようなエステル含有活性成分としては、例えば、英国特許第1 ,561.808号明細書に開示され且つ例えばEP−A第345 842号明 細書に更に開示されているイミダシリンエステル誘導体が挙げられている。Therefore, ester-containing fabric softening actives can be substituted for typical quaternary softening actives. Discloses that it should be used as a replacement or in combination with regular quaternary softening active ingredients has been done. Such ester-containing active ingredients include, for example, British Patent No. , 561.808 and e.g. EP-A No. 345 842. Mention is made of imidacillin ester derivatives which are further disclosed in the specification.

しかしながら、前記エステルイミダシリン化合物を含有する濃縮組成物は、長期 貯蔵時に異臭(off−note)を生ずる傾向を有することが見出されている 。However, concentrated compositions containing said ester imidacillin compounds are not suitable for long-term use. It has been found that it has a tendency to produce off-notes when stored. .

本発明は、このような問題が少量の重金属イオン用キレート化剤を前記濃縮組成 物へ配合することによって驚異的なことに解消されるという発見に基づく。The present invention solves this problem by adding a small amount of chelating agent for heavy metal ions to the concentrated composition. This is based on the discovery that the problem can be solved miraculously by adding it to products.

米国特許第3,756,950号明細書には、布帛きばみを少なくするために通 常の第四級アンモニウム柔軟化活性成分とアミノカルボン酸キレート化剤の酸性 塩とを含有する布帛柔軟化組成物が開示されている。U.S. Pat. No. 3,756,950 discloses a method for reducing fabric shear. Acidity of conventional quaternary ammonium softening active ingredients and aminocarboxylic acid chelators Fabric softening compositions containing a salt are disclosed.

本発明は、式 (式中、XおよびXlは独立にC1l〜C21ヒドロカルビル基、好ましくはC 13〜C17アルキルであり、mおよびnは独立に2〜4、好ましくは2である )のイミダシリンエステル柔軟化活性成分中なくとも10重量%、好ましくは1 5〜25重量%およびpH4以下を有するような量としてのブレンステッド酸を 含有する濃縮布帛柔軟化組成物であって、組成物の0.01%〜1%、好ましく は0.05〜0.2%の量の重金属イオン用キレート化剤を含有することを特徴 とする濃縮布帛柔軟化組成物を包含する。The present invention is based on the formula (wherein X and Xl are independently C11 to C21 hydrocarbyl groups, preferably C11 to C21 hydrocarbyl groups, preferably C 13-C17 alkyl, m and n are independently 2-4, preferably 2 ), preferably at least 10% by weight in the imidacillin ester softening active ingredient of Brønsted acid in such an amount as to have 5 to 25% by weight and a pH below 4. A concentrated fabric softening composition comprising 0.01% to 1% of the composition, preferably is characterized by containing a chelating agent for heavy metal ions in an amount of 0.05-0.2% Concentrated fabric softening compositions are included.

本発明の組成物は、式 (式中、XおよびXlは独立にC−Cヒドロ力ルビル基、好ましくは013〜C 17アルキル、最も好ましくは直鎖C17アルキルであり、mおよびnは独立に 2〜4であり、好ましくはmおよびnは両方とも2である)を有する置換イミダ シリンエステル柔軟化化合物受なくとも10%、好ましくは15%〜25%を含 有する。柔軟剤活性成分の合計濃度は、約40重量%を超えることができない。The composition of the invention has the formula (wherein X and Xl are independently C-C hydrorubyl groups, preferably 013-C 17 alkyl, most preferably straight chain C17 alkyl, where m and n are independently 2-4, preferably m and n are both 2) Contains at least 10%, preferably 15% to 25%, of a syringe ester softening compound. have The total concentration of softener active ingredients cannot exceed about 40% by weight.

置換基XおよびXlは、場合によって、アルコキシル、ヒドロキシルなどの各種 の基で置換してもよく、または分枝であることができるが、このような物質は、 ここで好ましくないことが理解されるであろう。Substituents X and Xl may optionally be various groups such as alkoxyl, hydroxyl, etc. may be substituted or branched with groups such as It will be understood that there is something objectionable here.

加えて、Xおよび/またはXlは、場合によって、不飽和であってもよい(即ち 、アルケニル基)。好ましい置換イミダシリンエステル柔軟化化合物は、以下、 ジアルキルイミダシリンエステル化合物と称するであろう。シタローイミダシリ ンエステルが、最も好ましい。Additionally, X and/or Xl may optionally be unsaturated (i.e. , alkenyl group). Preferred substituted imidacilline ester softening compounds are: They will be referred to as dialkylimidacyline ester compounds. Shitaro Imida Shiri most preferred.

pH 本組成物の3%希釈度での蒸留水で測定されたpHは、4以下、好ましくは2. 5〜4であるべきである。pH The pH of the composition measured in distilled water at 3% dilution is below 4, preferably 2. Should be 5-4.

このようなpHを達成するためには、pKa値6以下を有するブレンステッド酸 は、本組成物に存在する。To achieve such a pH, a Brønsted acid with a pKa value of 6 or less must be used. is present in the composition.

好適な酸の例としては、無機鉱酸、カルボン酸、特に低分子量(C−C5)カル ボン酸、芳香族カルボン酸、例えば、安息香酸、およびアルキルスルホン酸が挙 げられる。Examples of suitable acids include inorganic mineral acids, carboxylic acids, especially low molecular weight (C-C5) carboxylic acids. Bonic acids, aromatic carboxylic acids such as benzoic acid, and alkylsulfonic acids are mentioned. can be lost.

好適な無機酸としては、HC1,HB r、H2SO4、HNOおよびH3PO 4が挙げられる。好適な有機酸としては、安息香酸、ギ酸、酢酸、メチルスルホ ン酸およびエチルスルホン酸が挙げられる。好ましい酸は、リン酸、ギ酸、およ びメチルスルホン酸である。Suitable inorganic acids include HC1, HBr, H2SO4, HNO and H3PO 4 can be mentioned. Suitable organic acids include benzoic acid, formic acid, acetic acid, methyl sulfonate. ethylsulfonic acid and ethylsulfonic acid. Preferred acids are phosphoric acid, formic acid, and and methylsulfonic acid.

液体担体 本組成物は、液体担体、例えば、水、好ましくは水と01〜C4−価アルコール (例えば、エタノール、プロパツール、イソプロパツール、ブタノール、および これらの混合物)との混合物を含み、イソプロパツールが好ましい。これらの組 成物は、液体担体60%〜98%、好ましくは70%〜95%を含む。好ましく は、液体担体中のC1〜C4−価アルコールの量は、柔軟化化合物の5〜50重 量%であり、液体担体の残部は水である。liquid carrier The composition comprises a liquid carrier, such as water, preferably water and a 01-C4-hydric alcohol. (e.g. ethanol, propatool, isoproptool, butanol, and mixtures thereof), with isopropanol being preferred. these pairs The composition contains 60% to 98%, preferably 70% to 95% liquid carrier. preferably The amount of C1-C4-hydric alcohol in the liquid carrier is 5-50% by weight of the softening compound. % by volume, with the remainder of the liquid carrier being water.

重金属イオン用キレート化剤 キレート化剤は、本組成物の0.01%〜1%、好ましくは0.05〜0.2% の量で存在する。Chelating agent for heavy metal ions The chelating agent comprises 0.01% to 1% of the composition, preferably 0.05 to 0.2%. exists in an amount of

ここで有用な重金属イオン用キレート化剤としては、その目的で技術上既知のい かなる物質も挙げられる。Chelating agents for heavy metal ions useful herein include any known in the art for that purpose. Any substance may also be mentioned.

好適な化合物としては、下記のカルボン酸およびこれらの塩が挙げられる:クエ ン酸、酒石酸、オキシジコハク酸、エチレンジアミン−N、N−ジコハク酸、オ キシ二酢酸、カルボキシメチルタルトロン酸、カルボキシメチルオキシコハク酸 、80:20の重量比のタルトレートモノコハク酸/タルトレートジコハク酸ブ レンド、並びに2−ドデセニルコハク酸、およびドデシルコハク酸。Suitable compounds include the following carboxylic acids and their salts: acid, tartaric acid, oxydisuccinic acid, ethylenediamine-N, N-disuccinic acid, oxydisuccinic acid, xydiacetic acid, carboxymethyl tartronic acid, carboxymethyloxysuccinic acid , tartrate monosuccinic acid/tartrate disuccinate in a weight ratio of 80:20. Lend, and 2-dodecenylsuccinic acid, and dodecylsuccinic acid.

このカテゴリーは、ポリカルボン酸およびこれらの塩、例えば、ポリアクリレー トおよびマレイン酸とアクリル酸との共重合体も包含する。This category includes polycarboxylic acids and their salts, such as polyacrylates. It also includes copolymers of maleic acid and acrylic acid.

他の好適な化合物は、下記のアミノカルボン酸およびこれらの塩、例えば、ニト リロ三酢酸、エチレンジアミン四酢酸、シクロエチレンジアミン四酢酸、tra ns 1 。Other suitable compounds are the aminocarboxylic acids and salts thereof, such as nitrates described below. Lilotriacetic acid, ethylenediaminetetraacetic acid, cycloethylenediaminetetraacetic acid, tra ns 1 .

2ジアミノシクロヘキサンN、N、N’ 、N’四酢酸1水和物(CHELCD ) 、ヒドロキシエチレンジアミン四酢酸、ジエチレントリアミノ五酢酸、N− グリセリルイミノニ酢酸、N(−2ヒドロキシプロピル)イミノニ酢酸である。2 Diaminocyclohexane N, N, N', N' Tetraacetic acid monohydrate (CHELCD ), hydroxyethylenediaminetetraacetic acid, diethylenetriaminopentaacetic acid, N- These are glyceryl iminodiacetic acid and N(-2hydroxypropyl)iminodiacetic acid.

ポリアミノポリアルキレンホスホン酸およびこれらの塩、例えば、エチレンジア ミンテトラメチレンホスホン酸およびジエチレントリアミンペンタメチレンホス ホン酸も、本発明のキレート化剤として好適である。Polyaminopolyalkylenephosphonic acids and their salts, e.g. ethylenedia Minetetramethylenephosphonic acid and diethylenetriaminepentamethylenephos Ponic acid is also suitable as a chelating agent in the present invention.

任意成分 完全に処方された布帛柔軟化組成物は、場合によって、前記式の置換イミダシリ ンエステル柔軟化化合物、液体担体および酸に加えて、下記の成分の1種以上を 含有し本発明の組成物は、ジ(高級アルキル)第四級アンモニウム柔軟剤を更に 含むことができる。本組成物は、ジ(高級アルキル)第四級アンモニウム柔軟剤 0%〜25%(好ましくは0.1%〜10%)を含有できる。Optional ingredients The fully formulated fabric softening composition optionally comprises a substituted imidasyl of the formula In addition to the ester softening compound, liquid carrier, and acid, one or more of the following ingredients may be added: The composition of the present invention further comprises a di(higher alkyl) quaternary ammonium softener. can be included. This composition is a di(higher alkyl) quaternary ammonium softener. It can contain 0% to 25% (preferably 0.1% to 10%).

ここで有用な第四級柔軟剤は、下記のものの群から選(式中、R2はエステル基 によって中断されていてもよい非環式脂肪族C−C炭化水素基であり、R3は0 1〜C4飽和アルキルまたはヒドロキシアルキル基であり、RはRおよびR3か ら選ばれ、Aは陰イオンである) を有する非環式第四級アンモニウム塩(R2および場合によってR4がエステル 基によって中断されている式(i)の迅速生分解性化合物はEPA第239 9 10号明細書に開示されている); (II)式 (式中、Roは非環式脂肪族C15〜C2゜炭化水素基であり、R2は炭素数1 〜3の二価のアルキレン基であり、RおよびR8はC1〜C4飽和アルキルまた はヒドロキシアルキル基であり、A−は陰イオンである)を有するジアミド第四 級アンモニウム塩;(111)式 (式中、nは1〜5に等しく、RR l・ 2・R5および A−は上に定義の通りである) を有するジアミドアルコキシ化第四級アンモニウム塩;(1v)式 (式中、RはC−C飽和アルキルであり、’R2は01〜C4飽和アルキルであ り、2はNHまたはOであり、A−は陰イオンである) を有する第四級イミダゾリニウム化合物。Quaternary softeners useful herein are selected from the group of: (wherein R2 is an ester group) is an acyclic aliphatic C-C hydrocarbon group optionally interrupted by R3 is 0 1-C4 saturated alkyl or hydroxyalkyl group, R is R and R3 or and A is an anion) (where R2 and optionally R4 are esters) Rapidly biodegradable compounds of formula (i) which are interrupted by groups are EPA No. 2399 10); (II) Formula (In the formula, Ro is an acyclic aliphatic C15-C2° hydrocarbon group, and R2 has 1 carbon number. -3 divalent alkylene group, R and R8 are C1-C4 saturated alkyl or is a hydroxyalkyl group and A- is an anion) class ammonium salt; formula (111) (where n is equal to 1 to 5 and RR l・ 2・R5 and A- is as defined above) A diamide alkoxylated quaternary ammonium salt having the formula (1v) (In the formula, R is C-C saturated alkyl, and 'R2 is 01-C4 saturated alkyl. (2 is NH or O, A- is an anion) A quaternary imidazolinium compound having

成分(i)の例は、周知のジアルキルジメチルアンモニウム塩、例えば、シタロ ージメチルアンモニウムクロリド、シタロージメチルアンモニウムメチルサルフ ェート、ジ(水素添加タロー)ジメチルアンモニウムクロリド、ジベヘニルジメ チルアンモニウムクロリドである。Examples of component (i) are the well-known dialkyldimethylammonium salts, such as citalo. -Dimethylammonium chloride, Citalodimethylammonium methylsulfate ate, di(hydrogenated tallow)dimethylammonium chloride, dibehenyldime It is tylammonium chloride.

成分(11)および(111)の例は、R1が非環式脂肪族C−C炭化水素基、 R2がエチレン基、R5がメチ15 1フ ル基、R8がヒドロキシアルキル基、Aがメチルサルフェート陰イオンであるメ チルビス(タローアミドエチル)(2−ヒドロキシエチル)アンモニウムメチル サルフェートおよびメチルビス(水素添加タローアミドエチル)(2−ヒドロキ シエチル)アンモニウムメチルサルフェートである。これらの物質は、シエレッ クス・ケミカル・カンパニーからそれぞれ商品名パリソフト(Varisol’ t ) 222およびパリソフトR110で入手できる。Examples of components (11) and (111) include R1 being an acyclic aliphatic C-C hydrocarbon group; R2 is ethylene group, R5 is methyl 15 1-phrase group, R8 is a hydroxyalkyl group, and A is a methyl sulfate anion. Chilbis(tallowamidoethyl)(2-hydroxyethyl)ammonium methyl sulfate and methylbis(hydrogenated tallowamide ethyl)(2-hydroxy ethyl) ammonium methyl sulfate. These substances The product name is Varisol' from Kusu Chemical Company. t) 222 and Parisoft R110.

成分(1v)の例は、]−]メチルー1−タローアミノエチル2−タローイミダ ゾリニウムメチルサルフェートおよび1−メチル−1−(水素添加タローアミド エチル)メチルサルフェートである。An example of component (1v) is ]-]methyl-1-tallowaminoethyl 2-tallowimida Zolinium methyl sulfate and 1-methyl-1-(hydrogenated tallowamide) ethyl) methyl sulfate.

第四級アンモニウム塩対環式アミンの比率は、10:1を超えるべきではなく、 好ましくは2:1を超えない。The ratio of quaternary ammonium salt to cyclic amine should not exceed 10:1; Preferably it does not exceed 2:1.

第四級柔軟剤の水性分散液は、常法で調製し、典型的には、連続的な攪拌下に溶 融形の第四級物質を水を含有するバッチに注入することによって調製する。Aqueous dispersions of quaternary softeners are prepared in a conventional manner and are typically dissolved under continuous stirring. The quaternary material in molten form is prepared by injecting it into a batch containing water.

一旦この分散液を調製したら、工程(a)〜(d)から生ずる濃縮組成物は、そ れに加えられるであろう。Once this dispersion is prepared, the concentrated composition resulting from steps (a) to (d) is will be added to this.

連続法の場合には、前記濃縮組成物は、工程(d)直後に、第四級アンモニウム 化合物の水性分散液に加えられるであろう。In the case of a continuous process, the concentrated composition is treated with quaternary ammonium immediately after step (d). It will be added to the aqueous dispersion of the compound.

別の好都合な方法においては、工程(d)後に得られる濃縮組成物を、先ず、1 5〜25℃の温度(室温)に冷却し、次いで、第四級柔軟剤の水性分散液に加え る前に、例えば、濃縮組成物の貯蔵、輸送のために若干の時間が許容されるであ ろう。In another convenient method, the concentrated composition obtained after step (d) is first Cool to a temperature of 5-25 °C (room temperature) and then add to the aqueous dispersion of quaternary softener. For example, some time may be allowed for storage and transportation of the concentrated composition before Dew.

いかなる場合にも、完成品の粘度は、20〜500 cp。In any case, the viscosity of the finished product is between 20 and 500 cp.

好ましくは50〜150cpの範囲内とされるであろう。Preferably it will be within the range of 50 to 150 cp.

任意の補助柔軟剤 ここで使用する補助柔軟剤(co−softening agent)は、8個 までの炭素原子を有する多価アルコールの脂肪酸エステル、例えば、DE−A第 26 31. 114号明細書に記載のものから選ぶことができる。このような エステルの例としては、ソルビタンエステルおよびグリセロールエステル、例え ば、ソルビタンモノステアレート、ソルビタンモノオレエート、グリセロールモ ノ−ジーおよびトリー脂肪酸エステル(酸はステアリン酸、オレイン酸、ラウリ ン酸、カプリン酸、カプリル酸、カプロン酸、吉草酸、酪酸、プロピオン酸およ び酢酸から選ばれる)が挙げられる。個々のグリセロールは、同一の脂肪酸基に より、または混合エステルによりエステル化できる(例えば、グリセロールモノ ステアレートリオレエート)。ポリエチレングリコール部分が分子量200〜4 00を有するポリエチレングリコールエステルモノステアレートも、その種類に 包含される。炭素数少なくとも4の一価アルコールの脂肪酸エステル、例えば、 ステアリン酸イソブチルおよびステアリン酸エチルヘキシルも、有用であること がある。Optional auxiliary softener There are 8 co-softening agents used here. Fatty acid esters of polyhydric alcohols having carbon atoms up to, e.g. 26 31. It can be selected from those described in the specification of No. 114. like this Examples of esters include sorbitan esters and glycerol esters, e.g. For example, sorbitan monostearate, sorbitan monooleate, glycerol molybdenum Nosy and tri fatty acid esters (acids include stearic acid, oleic acid, lauric acid) acid, capric acid, caprylic acid, caproic acid, valeric acid, butyric acid, propionic acid and and acetic acid). Individual glycerols have the same fatty acid group or by mixed esters (e.g. glycerol mono stearate trioleate). The polyethylene glycol part has a molecular weight of 200 to 4. Polyethylene glycol ester monostearate with 00 is also included in its type. Included. Fatty acid esters of monohydric alcohols having at least 4 carbon atoms, e.g. Isobutyl stearate and ethylhexyl stearate are also useful. There is.

使用できる追加の補助柔軟剤は、グリセロール、ジグリセロール、エチレングリ コール、プロピレングリコ−ル、ジエチレングリコール、ジプロピレングリコー ル、ジエチレングリコール、ポリエチレングリコール(分子量200〜100, 000)、ポリプロピレングリコール(分子量200〜100,000)、ポリ ビニルアルコール、ポリオキシエチレンポリオキシブロビレン共重合体、ポリプ ロピレングリコール(分子j1900)、グルコースメチルエーテル、ブチルジ グリコールエーテル、ジエチレングリコールモノブチルエーテル、プロピレング リコールモノエチルまたはエチルエーテル、炭酸エチレン、炭酸プロピレンであ る。Additional auxiliary softeners that can be used are glycerol, diglycerol, and ethylene glycerol. Coal, propylene glycol, diethylene glycol, dipropylene glycol diethylene glycol, polyethylene glycol (molecular weight 200-100, 000), polypropylene glycol (molecular weight 200-100,000), polypropylene glycol (molecular weight 200-100,000), Vinyl alcohol, polyoxyethylene polyoxybrobylene copolymer, polypropylene Ropylene glycol (molecule j1900), glucose methyl ether, butyl di Glycol ether, diethylene glycol monobutyl ether, propylene Recall monoethyl or ethyl ether, ethylene carbonate, propylene carbonate. Ru.

一般式 RO(Cn H2n O) t (グルコシル)X(式中、R2はアル キル、アルキルフェニル、ヒドロキシアルキル、ヒドロキシアルキルフェニルお よびこれらの混合物であり、アルキル鎖は8〜18個の炭素原子を有し、tは0 〜2であり、Xは2〜7である)のアルキルポリグルコシドも、有用であり、本 組成物で使用できる。これらのグルコシドは、望ましい溶剤特性を示し且つ更に 柔軟性などの利益を繊維に与えることができる。General formula RO (Cn H2n O) t (glucosyl) Kyl, alkylphenyl, hydroxyalkyl, hydroxyalkylphenyl and mixtures thereof, the alkyl chain has 8 to 18 carbon atoms, and t is 0 ~2 and X is 2 to 7) are also useful and described herein. Can be used in compositions. These glucosides exhibit desirable solvent properties and further Benefits such as flexibility can be imparted to the fiber.

ラノリンおよび誘導体および炭素数16〜20のパラフィンは、所望ならば使用 できる非イオン剤の別の例を構成する。動物、植物または鉱物起源の低融点油は 、この種の物質を代表している。カーネーションφオイル(Carnatlon  oil ) 、ジジジョバ・オイル(JojobaollR)およびヒマワリ 油は、機能することが見出された特定例である。Lanolin and derivatives and C16-20 paraffins can be used if desired. constitute another example of a nonionic agent that can be used. Low melting point oils of animal, vegetable or mineral origin are , is representative of this type of substance. Carnation φ oil (Carnatlon) oil), Jijijoba oil (JojobaollR) and sunflower Oil is a specific example that has been found to work.

別の重要な種類の補助柔軟剤は、一般式%式% (式中、R1は炭素数8〜23の直鎖または分枝鎖アルキルまたはアルケニル基 であり、R2は水素または炭素数1〜4のアルキルまたはヒドロキシアルキル基 である)の物質で表わされる。Another important type of auxiliary softener is the general formula % formula % (In the formula, R1 is a straight chain or branched alkyl or alkenyl group having 8 to 23 carbon atoms. and R2 is hydrogen or an alkyl or hydroxyalkyl group having 1 to 4 carbon atoms. ) is expressed as a substance.

この種の高度に好ましい物質は、C1(1” 20飽和脂肪酸、特にラウリン酸 、ミリスチン酸、パルミチン酸およびステアリン酸である。Highly preferred substances of this type are C1 (1"20 saturated fatty acids, especially lauric acid , myristic acid, palmitic acid and stearic acid.

BASFから入手できルルテンソル(LUTENSOLo)化合物などの線状脂 肪08〜18アルカノールエトキシレート並びにエクソンから入手できるエキサ ール(EXXAL)化合物などの分枝Cアルカノールも、好適である。Linear fats such as the LUTENSOLo compound available from BASF fat 08-18 alkanol ethoxylates and extracts available from Exxon Branched C alkanols such as EXXAL compounds are also suitable.

8〜18 粘土物質、例えば、EPA第150.531号明細書に記載の低イオン交換容量 のものも、使用できる。8-18 Clay materials, such as low ion exchange capacity as described in EPA 150.531 You can also use those.

前記補助柔軟剤は、陽イオン活性アミン、即ち、炭素数12〜22の直鎖有機基 中なくとも1個を有する第一級、第二級および第三級アミンと併用できる。この 種の好ましいアミンは、1分子当たり合計2〜30個のエトキシ基を有するモノ タロー−ジボリエトキシアミンなどのエトキシアミンである。ジアミン、例えば 、タロー−N、N’ 、N’ −トリス(2−ヒドロキシエチル)−1゜3−プ ロピレンジアミン、またはCI6〜18アルキル−N−ビス(2−ヒドロキシエ チル)アミンも、好適である。The co-softener is a cationically active amine, i.e., a linear organic group having 12 to 22 carbon atoms. It can be used in combination with at least one primary, secondary and tertiary amine. this Preferred amines of the species are monomers having a total of 2 to 30 ethoxy groups per molecule. Ethoxyamines such as tallow-dibolyethoxyamine. Diamines, e.g. , tallow-N, N', N'-tris(2-hydroxyethyl)-1゜3-propylene propylene diamine, or CI6-18 alkyl-N-bis(2-hydroxyethyl) Chil)amines are also suitable.

前記アミンの例は、ヘキストによって商品名ゲナミン(GENAMIN)C,S 、 DおよびTで販売されているものである。Examples of said amines include the trade name GENAMIN C,S by Hoechst. , D and T.

前記補助柔軟剤は、第四級柔軟剤対補助柔軟剤の比率5:1から20:1で使用 される。The co-softener is used in a quaternary softener to co-softener ratio of 5:1 to 20:1. be done.

脂肪酸を使用する場合には、好ましい比率は、8二1から10=1である。When using fatty acids, the preferred ratio is 821 to 10=1.

ここで使用するための更に他の任意成分としては、シリコーン成分、例えば、英 国特許第1.549,180号明細書に記載のもの、乳化剤、防腐剤、殺菌剤、 染料、殺細菌剤、安定剤、増白剤、乳白剤、光活性剤、金属イオン封鎖性を有す る共重合体カルボキシレート、防汚剤、漂白剤、漂白活性剤、およびきばみ防止 剤が挙げられる。Still other optional components for use herein include silicone components, e.g. Those described in National Patent No. 1.549,180, emulsifiers, preservatives, bactericides, Dyes, bactericides, stabilizers, brighteners, opacifiers, photoactivators, sequestering properties Copolymer carboxylates, antifouling agents, bleaching agents, bleach activators, and anti-scratch agents Examples include agents.

好適な重合体防汚剤は、EP−A第220 156号明細書に開示されている。Suitable polymeric antifouling agents are disclosed in EP-A 220 156.

これらの添加剤は、通常、本濃縮物の希釈工程において、通常の少量、例えば、 0.001%〜5%で配合される。These additives are usually added in small amounts in the dilution process of the concentrate, e.g. It is blended at 0.001% to 5%.

下記の例は、本発明を例示する。The following examples illustrate the invention.

表1 例1 例2 シタローイミダシリンエステル 2022香料 o、go o、g。Table 1 Example 1 Example 2 Citalo imidacillin ester 2022 fragrance o, go o, g.

ポリジメチルシロキサン 0.2 0.2防汚重合体 0.2 0.2 クエン酸 0.1 G、05 Ca C120,20,2 水および微量成分 残部 pH3% 3.0 例1および2の組成物を50℃で3週間貯蔵し、同じ条件下で貯蔵したクエン酸 を含有しない同様の組成物と比較した。例1および2の組成物は、対照組成物に 反して香料異臭を生じなかった。Polydimethylsiloxane 0.2 0.2 Antifouling polymer 0.2 0.2 Citric acid 0.1G, 05 Ca C120,20,2 Water and trace ingredients balance pH 3% 3.0 The compositions of Examples 1 and 2 were stored at 50°C for 3 weeks and citric acid stored under the same conditions. compared to a similar composition containing no. The compositions of Examples 1 and 2 were compared to the control composition. On the contrary, no fragrance odor was produced.

下記の組成物も調製する。The following compositions are also prepared.

表2 例3 例4 例5 例6 ジタローイミダゾリンエステル 21 22 23 23香料 0.7 0.7  0.8 0.7ポリジメチルシロキサン 0.2 − 0.2 −防汚重合体  0.2 0.2 − − デクエスト(Dequest、) 2066★ 0.1 − − −EDTA二 ナトリウム塩 −0,1− CHELCD★★ −−ロ、05 − 酒石酸 −−−0,1 水および微量成分 残部 pH3% 3.0 ★ジエチレントリアミンペンタメチレンホスホン酸★★trans 1. 2ジ アミノシク口ヘキサジN、 N、 N’ 、 N’四酢酸1水和物Table 2 Example 3 Example 4 Example 5 Example 6 Ditalo imidazoline ester 21 22 23 23 Fragrance 0.7 0.7 0.8 0.7 Polydimethylsiloxane 0.2 - 0.2 - Antifouling polymer 0.2 0.2 − − Dequest (Dequest,) 2066★ 0.1 - - -EDTA 2 Sodium salt -0,1- CHELCD★★--Ro, 05- Tartaric acid---0,1 Water and trace ingredients balance pH 3% 3.0 ★Diethylenetriaminepentamethylenephosphonic acid★★trans 1. 2 ji Aminosic hexadiN, N, N', N'tetraacetic acid monohydrate

Claims (7)

【特許請求の範囲】[Claims] 1.式 ▲数式、化学式、表等があります▲ (式中、XおよびX1は独立にC11〜C21ヒドロカルビル基、好ましくはC 13〜C17アルキルであり、mおよびnは独立に2〜4、好ましくは2である )のイミダゾリンエステル柔軟活性成分少なくとも10重量%およびpH4以下 を有するような量としてのブレンステッド酸を含有する濃縮布帛柔軟化組成物で あって、組成物の0.01%〜1%の量の重金属イオン用キレート化剤を含有す ることを特徴とする濃縮布帛柔軟化組成物。1. formula ▲ Contains mathematical formulas, chemical formulas, tables, etc. ▲ (wherein X and X1 are independently C11-C21 hydrocarbyl groups, preferably C 13-C17 alkyl, m and n are independently 2-4, preferably 2 ) of at least 10% by weight of the imidazoline ester softening active ingredient and a pH of 4 or less In a concentrated fabric softening composition containing a Brønsted acid in an amount such that and contains a chelating agent for heavy metal ions in an amount of 0.01% to 1% of the composition. A concentrated fabric softening composition characterized by: 2.前記イミダゾリンエステルが、ジタローイミダソリンエステルである、請求 項1に記載の組成物。2. Claim wherein the imidazoline ester is a ditallow imidasoline ester. Item 1. The composition according to item 1. 3.前記キレート化剤が、カルボン酸、ポリカルボン酸、アミノカルボン酸、ポ リアミノポリアルキレンホスホン酸、およびこれらの塩の群から選ばれる、請求 項1または2に記載の組成物。3. The chelating agent is carboxylic acid, polycarboxylic acid, aminocarboxylic acid, polycarboxylic acid, Claimed to be selected from the group of riaminopolyalkylenephosphonic acids, and salts thereof. Item 2. The composition according to item 1 or 2. 4.前記前記キレート化剤が、クエン酸、EDTA、およびジエチレントリアミ ンペンタメチレンホスホン酸の群から選ばれる、請求項3に記載の組成物。4. The chelating agent may include citric acid, EDTA, and diethylene triamine. 4. A composition according to claim 3, selected from the group of pentamethylenephosphonic acids. 5.キレート化剤の量が、0.05%〜0.2%である、請求項1〜4に記載の 組成物。5. Claims 1 to 4, wherein the amount of chelating agent is between 0.05% and 0.2%. Composition. 6.イミダゾリンエステルの量が、15%〜25%である、請求項1〜5に記載 の組成物。6. Claims 1 to 5, wherein the amount of imidazoline ester is 15% to 25%. Composition of. 7.組成物のpHが、2.5〜4である、請求項1〜6に記載の組成物。7. The composition according to claims 1 to 6, wherein the pH of the composition is 2.5 to 4.
JP5506335A 1991-09-27 1992-09-21 Concentrated fabric softening composition Pending JPH07505189A (en)

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EP0534009B1 (en) 1995-12-06
CA2119767A1 (en) 1993-04-01
AR246566A1 (en) 1994-08-31
EP0534009A1 (en) 1993-03-31
PT100908A (en) 1993-11-30
ES2080241T3 (en) 1996-02-01
IE922689A1 (en) 1993-04-07
WO1993006294A1 (en) 1993-04-01
MX9205493A (en) 1993-04-01

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