WO2001036737A1 - Softener composition - Google Patents

Softener composition Download PDF

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Publication number
WO2001036737A1
WO2001036737A1 PCT/JP2000/007897 JP0007897W WO0136737A1 WO 2001036737 A1 WO2001036737 A1 WO 2001036737A1 JP 0007897 W JP0007897 W JP 0007897W WO 0136737 A1 WO0136737 A1 WO 0136737A1
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WIPO (PCT)
Prior art keywords
carbon atoms
group
alkyl group
alkyl
general formula
Prior art date
Application number
PCT/JP2000/007897
Other languages
French (fr)
Japanese (ja)
Inventor
Hiromitsu Hayashi
Noriko Yamaguchi
Shuji Tagata
Ikuo Sugano
Original Assignee
Kao Corporation
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
Priority claimed from JP2000102428A external-priority patent/JP3389549B2/en
Priority claimed from JP2000114097A external-priority patent/JP3389550B2/en
Application filed by Kao Corporation filed Critical Kao Corporation
Priority to DE60027138T priority Critical patent/DE60027138T2/en
Priority to EP00974874A priority patent/EP1154068B1/en
Priority to US09/868,920 priority patent/US6780833B1/en
Publication of WO2001036737A1 publication Critical patent/WO2001036737A1/en

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Classifications

    • 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
    • C11D3/48Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
    • 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
    • C11D1/62Quaternary ammonium 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/835Mixtures of non-ionic with cationic 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/86Mixtures of anionic, cationic, and non-ionic 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/04Carboxylic acids or 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

Definitions

  • the present invention relates to softener compositions.
  • 7-36949 discloses a dilong chain alkyl (alkyl or alkenyl group having 6 to 24 carbon atoms which may be interrupted by an ether bond, an ester bond or an acid amide bond). And a mono-long-chain alkyl (alkyl or alkenyl group having 6 to 24 carbon atoms, which may be interrupted by a polyester bond, an ester bond or an acid amide bond), of a weight ratio of Disclosed is a softening composition for textile products having a pH of 2 to 5 containing a ratio of 9: 1 to 5: 5.
  • an antibacterial fiber softener composition suitable for imparting antibacterial performance to fibers, which is used in combination with a conventional fiber softener composition.
  • an antimicrobial fabric softener composition comprising one or more cationic antimicrobial agents in a greater amount required for antimicrobial performance.
  • the antibacterial water-soluble quaternary ammonium salt has the problem of reducing the softening effect, and it was necessary to sacrifice the softening effect to obtain a satisfactory antibacterial effect.
  • an object of the present invention is to provide a softener composition which suppresses body odor derived from sweat or the like for a long time and has an excellent softening effect.
  • the present invention provides (a) a quaternary ammonium compound represented by the following general formula (1), and (b)
  • a softener composition containing a quaternary ammonium compound represented by the general formula (2) and further containing a compound selected from the following component (c) or component (d): Z '(1)
  • R 1 R 2 each independently represents an alkyl group or an alkenyl group having 12 to 22 carbon atoms
  • X and Y each independently represent —COO—, CONR 7 —
  • ⁇ CO— one NR 7 CO—, preferably at least one is one CO
  • R 7 represents a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group.
  • R 3 and R ′′ 1 are each independently an alkylene group having 1 to 5 carbon atoms;
  • R 5 and R 6 are an alkyl group or a hydroxyalkyl group having 1 to 3 carbon atoms or R 1 —X—R 3 —
  • Z— is an anionic group.
  • R s represents an alkyl group or alkenyl group having 12 to 22 carbon atoms
  • W is a group selected from —CO—, one CONR 7 —, one OCO—, and one NR 7 CO—.
  • R 7 is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group, preferably Preferably, it is a hydrogen atom.
  • R 9 is an alkylene group having 5 to several carbon atoms
  • R 1 0, R 11 is an alkyl group or hydroxycarboxylic alkyl group having 1 to 3 carbon atoms
  • R 12 is alkyl of 1 to 3 carbon atoms Or —R 26 — ⁇ H.
  • R 26 is an alkylene group having 1 to 5 carbon atoms.
  • Z— is an anionic group.
  • R 13 and R 18 are each independently an alkyl group having 5 to 19 carbon atoms or an alkenyl group
  • R 14 and R 15 are each independently an alkyl group having 1 to 3 carbon atoms or It is a hydroxyalkyl group.
  • T is one COO-, one C-one, one CONH-,-NHCO
  • R 16 is an alkylene group having 1 to 3 carbon atoms
  • R 17 is an alkylene group having 1 to 6 carbon atoms or 1 (O—R 19 ) n—.
  • R 19 is an ethylene group or a propylene group
  • n is a number of 1 to 10.
  • W— is an anionic group.
  • R 2 . , R 2 ⁇ R 22 , R 23 is an alkyl group having 8 to 12 carbon atoms And the remainder is an alkyl group having 1 to 3 carbon atoms, a hydroxyalkyl group having 1 to 3 carbon atoms, or an arylalkyl group having 7 to 15 total carbon atoms, and Z— is an anionic group. . ]
  • the connecting hand means a covalent bond directly connecting R 13 and R 17 .
  • the component (a) of the present invention is a compound represented by the following general formula (1).
  • each of R 1 R 2 independently represents an alkyl group or alkenyl group having 12 to 22, preferably 14 to 22, and particularly preferably 14 to 18 carbon atoms
  • X and Y each represent independently, one COO-, one CONR 7 -, one OCO-, is an NR 7 CO- color selection Bareru groups, preferably at least one is _C_ ⁇ _ ⁇ one, -OCO-.
  • One COO— or one CONR 7 — is preferred.
  • R 7 represents a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group.
  • R 3 and R 4 are each independently an alkylene group having 1 to 5 carbon atoms;
  • R 5 and R 6 are an alkyl group or a hydroxyalkyl group having 1 to 3 carbon atoms or R 1 — X—R 3— and
  • Z— is an anionic group.
  • Z_ is preferably a halogen ion, a sulfate ion, a phosphate ion, an alkyl sulfate ion having 1 to 3 carbon atoms, or a fatty acid ion having 1 to 12 carbon atoms.
  • the following compounds are particularly preferred as the component (a).
  • R ′, R ′′ an alkyl group or an alkenyl group having 12 to 18 carbon atoms, which may be the same or different, R ′ ′′ ′ is an alkyl group or a hydroxyalkyl group having 1 to 3 carbon atoms, R "" is an alkyl group having 1 to 3 carbon atoms.
  • the component (b) of the present invention is a compound represented by the following general formula (2).
  • R 8 is 12 to 22 carbon atoms, preferably 14 to 22, particularly preferably an alkyl or alkenyl group of 14 ⁇ 1 8
  • W is one C_rei_0_, -CONR 7 one, ten C ⁇ one, one NR 7 CO—, preferably one COO— or one CONR 7 —.
  • R 7 represents a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group, preferably a hydrogen atom.
  • R 9 is an alkylene group having 1 to 5 carbon atoms, and R 1Q and R 11 each independently represent an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group.
  • R 12 is an alkyl group having 1 to 3 carbon atoms or one R 26 —OH.
  • R 26 is an alkylene group having 1 to 5 carbon atoms.
  • Z— is an anionic group, preferably a halogen ion, a fatty acid ion, or an alkyl sulfate ion having 1 to 3 carbon atoms. ].
  • the component (c) of the present invention is a compound represented by the above general formula (3) or (4), and the most preferred component (c) includes the following compounds. In the formula, Z— and have the meaning described above.
  • R is an alkyl group having 12 to 16 carbon atoms
  • R is an optionally branched alkyl group having 6 to 10 carbon atoms, m is a number of 1 to 5)
  • the component (d) of the present invention is a compound represented by the general formula (5). Acid ions or alkyl sulfate ions having 1 to 3 carbon atoms are preferred.
  • the softener composition of the present invention preferably contains the component (a) in an amount of 3 to 50% by weight, more preferably 3 to 40% by weight. /. And particularly preferably 5 to 35% by weight.
  • the component (b) weighs 0.5 to 10 weight. / 0 , preferably 0.5-5% by weight. Further, it is preferred from the viewpoint of the softening effect and the deodorizing effect that the component (a) contains the component Z (b) in a weight ratio of 80 / 20-99 / 1, particularly 85/15 to 951.
  • the component (c) is used in an amount of 0.1 to 15% by weight. /. , Preferably 1 to 15 weight. /. Particularly preferred is 3 to 10 weight. / 0 contained. Further, (c) / (a) is desirably 1Z30 to 1Z1, preferably 1Z10 0 to 1/1 by weight in terms of the feeling of clothing and the deodorizing effect.
  • the component (d) is preferably 0.1 to 15 weight. /. And more preferably 0.2 to 10 weights. / 0 , and (a) / (d) is 50Zl to 2Zl, preferably 30Zl to 2/1, more preferably 2 OZl to 2 ⁇ 1 ⁇ , is desirable from the viewpoint of the texture and deodorizing effect of clothing.
  • the softener composition of the present invention is preferably in the form of an aqueous solution obtained by diluting at least the component (a) and the component (c) or the component (b) and the component (d) with water.
  • the water used is preferably distilled water or ion-exchanged water. Further, it is desirable from the viewpoint of storage stability that water is contained in the composition in an amount of 40 to 90% by weight, more preferably 50 to 85% by weight, and particularly preferably 60 to 85% by weight.
  • the composition of the present invention is preferably adjusted to have a pH at 20 ° C. of 1 to 6, more preferably 2 to 5, particularly 2.5 to 4, from the viewpoint of deodorizing effect and storage stability.
  • a nonionic surfactant in addition to the components (a), (b), (c) and (d).
  • a nonionic surfactant a polyoxyethylene alkyl ether having at least one alkyl or alkenyl group having 8 to 20 carbon atoms is preferable, and a nonionic surfactant represented by the general formula (6) is particularly preferable.
  • R 24 is an alkyl group or an alkenyl group having 10 to 18 carbon atoms, preferably 12 to 18 carbon atoms
  • R 25 is an alkylene group having 2 or 3 carbon atoms, preferably an ethylene group. It is. p represents a number of 2 to 100, preferably 5 to 80, more preferably 1 to 80, and particularly preferably 20 to 60.
  • U is one O—, one CON— or —N—, q is 1 when U is — ⁇ one, and q is two when U is one CON— or one N—. ].
  • R 24 has the meaning described above. r is 8 to 100 when the component (c) is included, When the component (d) is contained, the number is 5 to 100, preferably 10 to 80, and more preferably 20 to 80. ] R 2 -0- (C 2 H 4 0) s (C 3 H 6 0) tH
  • R 24 has the meaning described above.
  • s and t are each independently 2 to 40, preferably 5 to 40, preferably s + t is a number from 10 to 80, and ethylene oxide and propylene oxide are random or block adducts. It may be.
  • R 24 has the above-mentioned meaning.
  • the sum of u and V is 5 to 100 when the component (c) is included, 10 to 80 when the component (d) is included, and preferably 5 to 80.
  • the amount of the nonionic surfactant is 0.5 to 10% by weight from the viewpoint of stability, preferably:! ⁇ 8% by weight.
  • (f) a fatty acid having 8 to 22 carbon atoms or a salt thereof is preferably 0.1 to 5% by weight, particularly preferably 0.5 to 3% by weight for the purpose of improving the texture of the textile product.
  • Fatty acids or salts thereof are power prillic acid, power pric acid, lauric acid, myristic acid, nonoremitic acid, stearic acid, oleic acid, or a mixture thereof, particularly selected from lauric acid, stearic acid, and oleic acid.
  • One or more types are good.
  • fatty acids having an alkyl composition derived from coconut oil, palm oil, palm kernel oil, and tallow are also preferable.
  • an ester compound of a saturated or unsaturated fatty acid having 8 to 22 carbon atoms and a polyhydric alcohol is contained in the composition in an amount of 0.1 to 10% by weight, especially 0.5 to 10% by weight.
  • the content be 5 to 5% by weight.
  • ester compound triglyceride, diglyceride, monodalicelide, and pentaerythritol mono, di, triester, and sorbitan esters are preferred.
  • an inorganic salt for example, calcium chloride
  • an inorganic salt for example, calcium chloride
  • surfactants such as fatty acid salts include sodium salts and magnesium salts, but inorganic salts mixed into the composition by use of such surfactants are not subject to the above restrictions.
  • storage stability can be achieved by blending a solvent component selected from ethanol, isopropanol, glycerin, ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, and polyoxyethylene phenyl ether. It is preferable from the viewpoint of properties. These solvent components are preferably incorporated in the composition in an amount of 0 to 20% by weight, more preferably 0.1 to 20% by weight, and particularly preferably 0.5 to 10% by weight. When ethanol is used, it is preferable to use polyoxyethylene alkyl ether sulfate-modified ethanol 8- 8-acetylated sucrose-modified ethanol.
  • the softener composition of the present invention contains a silicone and a fragrance (particularly preferably those represented by components (c) and (d) described in Japanese Patent Application Laid-Open No. Or a combination of components such as pigments.
  • a silicone and a fragrance particularly preferably those represented by components (c) and (d) described in Japanese Patent Application Laid-Open No. Or a combination of components such as pigments.
  • R a saturated alkyl group in which C18 and C16 are mixed (C18: C16
  • R a saturated alkyl group in which C18 and C16 are mixed (C18: C16
  • R a saturated alkyl group in which C17 and C15 are mixed (C17: C15
  • R a saturated alkyl group in which C17 and C15 are mixed (C17: C15
  • the softener compositions shown in Table 1 were prepared using the above compounds (Products 1 to 6 of the present invention and Comparative products 1 to 3). Two sweaters (100% cotton) were washed in a washing machine using a commercially available weak alkaline detergent (Kao Attack) (Toshiba 2-tub washing machine VH-360 S1, detergent concentration 0.0667 weight / , 30 L of tap water, water temperature 20 ° C, 10 minutes). After that, the washing liquid was drained, and after dehydration for 1 minute, 30 L of tap water was injected, rinsed for 5 minutes, and dewatered for 1 minute after drainage. After injecting 30 L of tap water again, 5 g of the softener composition shown in Table 1 was added to the mixture and stirred for 5 minutes. Then, it was dehydrated and dried for 12 hours in a constant temperature room at 70% humidity and 25 ° C.
  • Kao Attack Toshiba 2-tub washing machine VH-360 S1, detergent concentration 0.0667 weight / , 30 L of tap water, water
  • the above softening treatment was performed using the softener composition shown in Table 1 and the corresponding composition excluding the antibacterial component [(c) component or (d) component], and 10 panelists were compared with each other.
  • the evaluation was performed according to the following criteria, and the average score was obtained.
  • the smell of the clothes dried in the constant temperature room and the smell of the clothes after putting them on five men in their twenties for 12 hours was determined by 10 panelists (10 men in their 30s). Judgment was made according to the following criteria, and the average score was determined for each.
  • a softener composition having the composition shown in Table 2 (product 7111 of the present invention) was prepared in the same manner as in Example 1.
  • the fragrance used was a mixture of 100 parts by weight of the composition shown in Table 3 and 10 parts by weight of dipropylene glycol. When they were evaluated in the same manner as in Example 1, excellent odor control effect and softness were recognized in all cases.
  • Table 2 A softener composition having the composition shown in Table 2 (product 7111 of the present invention) was prepared in the same manner as in Example 1.
  • the fragrance used was a mixture of 100 parts by weight of the composition shown in Table 3 and 10 parts by weight of dipropylene glycol.
  • softener compositions shown in Table 4 were prepared. Five pieces of Wishash (100% cotton) and five pieces of towel (100% cotton) (total weight of clothing: 1.5 kg) were washed in a washing machine using a commercially available weak alkaline detergent (Kao Attack) (Toshiba 2-tub washing machine VH_360 S1, detergent concentration 0.0667% by weight, tap water 30L used, water temperature 20 ° G, 10 minutes). After that, the washing solution was drained, and after dehydration for 1 minute, 30 L of tap water was injected, rinsed for 5 minutes, and dewatered for 1 minute after drainage. Thereafter, 30 L of tap water was injected again, and then 7 ml of the composition shown in Table 1 was added thereto, followed by stirring for 5 minutes. After that, it was dehydrated and air-dried.
  • Kao Attack Toshiba 2-tub washing machine VH_360 S1, detergent concentration 0.0667% by weight, tap water 30L used, water temperature 20 ° G, 10 minutes.
  • Table 1 shows the average score of less than 0.8 as “ ⁇ ”, 0.8 or more and less than 1.2 as mouth, 1.2 or more and less than 1.7 as “ ⁇ ”, and 1.7 or more as “X”.
  • Table 1 shows the results when the average score was 2 or more, rated as ⁇ , 1 or more, but less than 1.5, as mouth, 0.5 or more, but less than 1 as ⁇ , and X, less than 0.5. +3: very soft than the control + 2; softer than the control + 1; slightly softer than the control 0; equivalent to the control
  • pH is adjusted by 10 N hydrochloric acid aqueous solution and 0 N sodium hydroxide aqueous solution.

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Abstract

A softener composition which contains a compound of general formula (1), a compound of general formula (2), and a quaternary ammonium compound having an antibacterial activity and is excellent in body-deodorant and softening effects wherein R?1, R2 and R8¿ are each C¿12-22? alkyl or alkenyl; X, Y and W are each a group selected from among -COO-, -CONR?7¿-, -OCO-, and -NR7CO- with either X or Y being -COO- or -OCO- (wherein R7 is H, C¿1-3? alkyl, or hydroxyalkyl); R?3, R4 and R9¿ are each C¿1-5? alkylene; R?5, R6, R10 and R11¿ are each C¿1-2? alkyl or hydroxyalkyl; R?12¿ is C¿1-3? alkyl or -C1-5-OH; and Z?-¿ is an anion.

Description

柔軟剤組成物 技術分野 Softener composition Technical field
本発明は柔軟剤組成物に関する。 背景技術  The present invention relates to softener compositions. Background art
従来、 柔軟剤には長鎖アルキル基を有する 4級アンモニゥム塩ゃ 3級ァミンの 酸塩などが用いられている。 また、 繊維製品の衛生や消臭の点から抗菌剤を柔軟 剤組成物に配合する試みがなされている。 特表平 1 0— 5 1 2 0 1 5号公報には 柔軟剤として水不溶性の 4級ァンモニゥム塩及び抗菌剤として水溶性 4級ァンモ 二ゥム塩を配合した柔軟剤組成物が開示されている。 また、 特開平 7— 3 6 4 9 号公報はジ長鎖アルキル (エーテル結合、 エステル結合又は酸アミ ド結合により 中断されていてもよい炭素数 6〜2 4のアルキル基又はアルケニル基) 型ァミン とモノ長鎖アルキル (ヱ一テル結合、 エステル結合又は酸アミ ド結合により中断 されていてもよい炭素数 6〜2 4のアルキル基又はアルケニル基) 型第四級アン モニゥム塩とを、 重量比 9 : 1乃至 5 : 5の割合で含有して成る p H 2〜 5の繊 維製品柔軟仕上剤組成物を開示する。 国際特許出願公開明細書 9 8 / 5 6 8 8 6 号公報は繊維に抗菌性能を付与するに適当な抗菌性繊維柔軟剤組成物であって従 来の繊維柔軟剤組成物とともに該柔軟剤に抗菌性能の為に要されるより多い量の カチオン抗菌剤の 1種以上から成る抗菌性繊維柔軟剤組成物を開示する。 しかし ながら抗菌性水溶性 4級アンモニゥム塩は柔軟効果を低下させるという問題があ り、 満足できる抗菌効果を得るためには柔軟効果を犠牲にする必要があった。 特 に室内で衣料を乾燥させたときの菌に起因する異臭や着用時の汗に由来する体臭 を長時間抑制できる抗菌性能と、 高い柔軟効果を両立できる組成物を得ることは 困難である。 発明の開示 Conventionally, quaternary ammonium salts and tertiary amine salts having long-chain alkyl groups have been used as softeners. Attempts have also been made to incorporate an antimicrobial agent into the softener composition from the viewpoint of hygiene and deodorization of textile products. Japanese Unexamined Patent Application Publication No. Hei 10-51212 discloses a softener composition containing a water-insoluble quaternary ammonium salt as a softener and a water-soluble quaternary ammonium salt as an antibacterial agent. I have. Japanese Patent Application Laid-Open No. 7-36949 discloses a dilong chain alkyl (alkyl or alkenyl group having 6 to 24 carbon atoms which may be interrupted by an ether bond, an ester bond or an acid amide bond). And a mono-long-chain alkyl (alkyl or alkenyl group having 6 to 24 carbon atoms, which may be interrupted by a polyester bond, an ester bond or an acid amide bond), of a weight ratio of Disclosed is a softening composition for textile products having a pH of 2 to 5 containing a ratio of 9: 1 to 5: 5. International Patent Application Publication No. 98/856886 discloses an antibacterial fiber softener composition suitable for imparting antibacterial performance to fibers, which is used in combination with a conventional fiber softener composition. Disclosed is an antimicrobial fabric softener composition comprising one or more cationic antimicrobial agents in a greater amount required for antimicrobial performance. However, the antibacterial water-soluble quaternary ammonium salt has the problem of reducing the softening effect, and it was necessary to sacrifice the softening effect to obtain a satisfactory antibacterial effect. Special In addition, it is difficult to obtain a composition that can achieve both an antibacterial property that can suppress an unpleasant odor caused by bacteria when the clothes are dried indoors and a body odor caused by sweat when worn for a long time and a high softening effect. Disclosure of the invention
従って本発明の課題は汗などに由来する体臭を長時間抑制し、 且つ柔軟効果に 優れる柔軟剤組成物を提供することにある。  Therefore, an object of the present invention is to provide a softener composition which suppresses body odor derived from sweat or the like for a long time and has an excellent softening effect.
本発明は、 (a) 下記一般式 (1) の 4級アンモニゥム化合物、 及び (b) 下記 The present invention provides (a) a quaternary ammonium compound represented by the following general formula (1), and (b)
—般式 (2) の 4級アンモニゥム化合物を含有し、 さらに下記 (c) 成分又は下 記 (d) 成分から選ばれる化合物を含有する柔軟剤組成物。 Z' (1)—A softener composition containing a quaternary ammonium compound represented by the general formula (2) and further containing a compound selected from the following component (c) or component (d): Z '(1)
Figure imgf000004_0001
Figure imgf000004_0001
〔式中、 R1 R2は、 それぞれ独立に、 炭素数 12〜22のアルキル基又はアル ケニル基を示し、 X、 Yは、 それぞれ独立に、 — COO—、 一 CONR7—、 一 [Wherein, R 1 R 2 each independently represents an alkyl group or an alkenyl group having 12 to 22 carbon atoms, and X and Y each independently represent —COO—, CONR 7 —,
〇CO—、 一 NR7CO—であり、 好ましくは少なくともいずれか一方は一 CO〇CO—, one NR 7 CO—, preferably at least one is one CO
O—、 一 O CO—である。 ここで R 7は水素原子、 炭素数 1〜3のアルキル基又 はヒ ドロキシアルキル基を示す。 R3、 R"1は、 それぞれ独立に、 炭素数 1〜5の アルキレン基であり、 R5、 R6は炭素数 1〜3のアルキル基もしくはヒ ドロキシ アルキル基又は R1— X— R3—であり、 Z—は陰イオン基である。〕
Figure imgf000004_0002
O—, one O CO—. Here, R 7 represents a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group. R 3 and R ″ 1 are each independently an alkylene group having 1 to 5 carbon atoms; R 5 and R 6 are an alkyl group or a hydroxyalkyl group having 1 to 3 carbon atoms or R 1 —X—R 3 — And Z— is an anionic group.]
Figure imgf000004_0002
[式中、 Rsは炭素数 1 2〜22のアルキル基又はアルケニル基を示し、 Wは— C OO—、 一 CONR7—、 一 OCO—、 一 NR7CO—から選ばれる基である。 こ こで R 7は水素原子、 炭素数 1〜3のアルキル基又はヒ ドロキシアルキル基、 好 ましくは水素原子である。 また、 R 9は炭素数 1〜 5のアルキレン基であり、 R1 0、 R11は炭素数 1〜3のアルキル基又はヒ ドロキシアルキル基であり、 R12は 炭素数 1〜3のアルキル基又は— R26—〇Hである。 ここで R26は炭素数 1〜5 のアルキレン基である。 Z—は陰イオン基である。 ] [Wherein, R s represents an alkyl group or alkenyl group having 12 to 22 carbon atoms, and W is a group selected from —CO—, one CONR 7 —, one OCO—, and one NR 7 CO—. Here, R 7 is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group, preferably Preferably, it is a hydrogen atom. Also, R 9 is an alkylene group having 5 to several carbon atoms, R 1 0, R 11 is an alkyl group or hydroxycarboxylic alkyl group having 1 to 3 carbon atoms, R 12 is alkyl of 1 to 3 carbon atoms Or —R 26 —〇H. Here, R 26 is an alkylene group having 1 to 5 carbon atoms. Z— is an anionic group. ]
(c) 下記一般式 (3) の化合物及び Z又は一般式 (4) の化合物を 0. 1〜1 5重量%、  (c) 0.1 to 15% by weight of a compound represented by the following general formula (3) and Z or a compound represented by the general formula (4),
W (3) W (3)
Figure imgf000005_0001
Figure imgf000005_0001
〔式中 R13、 R18は、 それぞれ独立に、 炭素数 5〜1 9のアルキル基又はアルケ ニル基であり、 R14、 R15は、 それぞれ独立に、 炭素数 1〜 3のアルキル基又は ヒ ドロキシアルキル基である。 Tは一COO—、 一〇C〇一、 一 CONH―、 - NHCO
Figure imgf000005_0002
Wherein R 13 and R 18 are each independently an alkyl group having 5 to 19 carbon atoms or an alkenyl group, and R 14 and R 15 are each independently an alkyl group having 1 to 3 carbon atoms or It is a hydroxyalkyl group. T is one COO-, one C-one, one CONH-,-NHCO
Figure imgf000005_0002
あるいは連結手である。 R 16は炭素数 1〜3のアルキレン基であり、 R 17は炭素 数 1〜6のアルキレン基又は一(O— R19)n—である。 ここで R 19はエチレン基 又はプロピレン基であり、 nは 1〜1 0の数である。 W—は陰イオン基である。〕 (d) 下記一般式 (5) の化合物を 0. 01〜1 5重量%、 好ましくは 0. 1〜 Or a connecting hand. R 16 is an alkylene group having 1 to 3 carbon atoms, and R 17 is an alkylene group having 1 to 6 carbon atoms or 1 (O—R 19 ) n—. Here, R 19 is an ethylene group or a propylene group, and n is a number of 1 to 10. W— is an anionic group. (D) 0.01 to 15% by weight, preferably 0.1 to 15% by weight of the compound of the following general formula (5)
W (5)W (5)
Figure imgf000005_0003
Figure imgf000005_0003
〔式中、 R2。、 R2\ R22、 R23の 2又は 3個が炭素数 8〜 1 2のアルキル基 であり、 残りが炭素数 1〜 3のアルキル基、 炭素数 1〜 3のヒ ドロキシアルキル 基又は総炭素数 7〜1 5のァリールアルキル基であり、 Z—は陰イオン基であ る。〕 [Wherein, R 2 . , R 2 \ R 22 , R 23 is an alkyl group having 8 to 12 carbon atoms And the remainder is an alkyl group having 1 to 3 carbon atoms, a hydroxyalkyl group having 1 to 3 carbon atoms, or an arylalkyl group having 7 to 15 total carbon atoms, and Z— is an anionic group. . ]
ここで、 連結手とは R 13と R 17とを直接つなぐ共有結合のことを指す。 発明の実施の形態 Here, the connecting hand means a covalent bond directly connecting R 13 and R 17 . Embodiment of the Invention
本発明の (a) 成分は下記一般式 (1) の化合物である。 Z- (1) The component (a) of the present invention is a compound represented by the following general formula (1). Z- (1)
Figure imgf000006_0001
Figure imgf000006_0001
〔式中、 R1 R 2それぞれ独立に、 炭素数 1 2〜22、 好ましくは 14〜22、 特に好ましくは 14〜1 8のアルキル基又はアルケニル基を示し、 X、 Yは、 そ れぞれ独立に、 一 COO—、 一 CONR7—、 一 OCO—、 一 NR7CO—から選 ばれる基であり、 好ましくは少なくともいずれか一方は _C〇〇一、 -OCO- である。 一 COO—又は一 CONR7—が好ましい。 ここで R7は水素原子、 炭素 数 1〜3のアルキル基又はヒ ドロキシアルキル基を示す。 R3、 R4は、 それぞれ 独立に、 炭素数 1〜5のアルキレン基であり、 R5、 R 6は炭素数 1〜 3のアルキ ル基もしくはヒ ドロキシアルキル基又は R1— X— R3—であり、 Z—は陰イオン 基である。 尚、 Z_はハロゲンイオン、 硫酸イオン、 リン酸イオン、 炭素数 1〜 3のアルキル硫酸エステルイオン、 炭素数 1〜1 2の脂肪酸イオンが好ましい。〕 (a) 成分として特に下記の化合物が好ましい。
Figure imgf000007_0001
(In the formula, each of R 1 R 2 independently represents an alkyl group or alkenyl group having 12 to 22, preferably 14 to 22, and particularly preferably 14 to 18 carbon atoms, and X and Y each represent independently, one COO-, one CONR 7 -, one OCO-, is an NR 7 CO- color selection Bareru groups, preferably at least one is _C_〇_〇 one, -OCO-. One COO— or one CONR 7 — is preferred. Here, R 7 represents a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group. R 3 and R 4 are each independently an alkylene group having 1 to 5 carbon atoms; R 5 and R 6 are an alkyl group or a hydroxyalkyl group having 1 to 3 carbon atoms or R 1 — X—R 3— and Z— is an anionic group. Z_ is preferably a halogen ion, a sulfate ion, a phosphate ion, an alkyl sulfate ion having 1 to 3 carbon atoms, or a fatty acid ion having 1 to 12 carbon atoms. The following compounds are particularly preferred as the component (a).
Figure imgf000007_0001
〔R'、 R'';同一又は異なっていても良い炭素数 12〜 18のアルキル基又はァ ルケニル基、 R' ' 'は炭素数 1〜 3のアルキル基又はヒ ドロキシアルキル基であり , R""は炭素数 1〜 3のアルキル基である。〕  [R ′, R ″: an alkyl group or an alkenyl group having 12 to 18 carbon atoms, which may be the same or different, R ′ ″ ′ is an alkyl group or a hydroxyalkyl group having 1 to 3 carbon atoms, R "" is an alkyl group having 1 to 3 carbon atoms. ]
本発明の (b) 成分は下記一般式 (2) の化合物である。  The component (b) of the present invention is a compound represented by the following general formula (2).
Z' (2)Z '(2)
Figure imgf000007_0002
Figure imgf000007_0002
〔式中、 R8は炭素数 12〜22、 好ましくは 14〜 22、 特に好ましくは 14 〜 1 8のアルキル基又はアルケニル基を示し、 Wは、 一 C〇0_、 -CONR7 一、 一〇C〇一、 一 NR7CO—、 好ましぐは一COO—又は一 CONR7—であ る。 ここで R7は水素原子、 炭素数 1〜3のアルキル基又はヒ ドロキシアルキル 基、 好ましくは水素原子を示す。 また、 R 9は炭素数 1〜5のアルキレン基であ り、 R1Q、 R11は、 それぞれ独立に、 炭素数 1〜 3のアルキル基又はヒ ドロキシ アルキル基を示す。 R12は炭素数 1〜3のアルキル基又は一 R26— OHである。 ここで R 26は炭素数 1〜5のアルキレン基である。 Z—は陰イオン基、 好ましく はハロゲンイオン、 脂肪酸イオン、 炭素数 1〜3のアルキル硫酸イオンである。〕。 本発明の (c) 成分は前記一般式 (3) 又は (4) の化合物であり、 最も好ま しい (c) 成分として下記の化合物を挙げることができる。 式中の Z—、 は前記 の意味を示す。
Figure imgf000008_0001
Wherein, R 8 is 12 to 22 carbon atoms, preferably 14 to 22, particularly preferably an alkyl or alkenyl group of 14 ~ 1 8, W is one C_rei_0_, -CONR 7 one, ten C〇one, one NR 7 CO—, preferably one COO— or one CONR 7 —. Here, R 7 represents a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group, preferably a hydrogen atom. R 9 is an alkylene group having 1 to 5 carbon atoms, and R 1Q and R 11 each independently represent an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group. R 12 is an alkyl group having 1 to 3 carbon atoms or one R 26 —OH. Here, R 26 is an alkylene group having 1 to 5 carbon atoms. Z— is an anionic group, preferably a halogen ion, a fatty acid ion, or an alkyl sulfate ion having 1 to 3 carbon atoms. ]. The component (c) of the present invention is a compound represented by the above general formula (3) or (4), and the most preferred component (c) includes the following compounds. In the formula, Z— and have the meaning described above.
Figure imgf000008_0001
(Rは炭素数 1 2〜1 6のアルキル基)
Figure imgf000008_0002
(R is an alkyl group having 12 to 16 carbon atoms)
Figure imgf000008_0002
(Rは分岐していてもよい炭素数 6〜1 0のアルキル基、 mは 1〜5の数)
Figure imgf000008_0003
(R is an optionally branched alkyl group having 6 to 10 carbon atoms, m is a number of 1 to 5)
Figure imgf000008_0003
(1 は炭素数8〜18のアルキル基である)  (1 is an alkyl group having 8 to 18 carbon atoms)
本発明の (d) 成分は前記一般式 (5) の化合物であり、 一般式 (5) 中、 W 一で示される陰イオン基は、 硫酸イオン、 ハロゲンイオン、 炭素数 1〜12の脂 肪酸ィオン又は炭素数 1〜 3のアルキル硫酸イオンが好ましい。  The component (d) of the present invention is a compound represented by the general formula (5). Acid ions or alkyl sulfate ions having 1 to 3 carbon atoms are preferred.
(柔軟剤組成物)  (Softener composition)
本発明の柔軟剤組成物は、 (a) 成分を 3〜50重量%含有するのが好ましく、 より好ましくは 3〜40重量。 /。、 特に好ましくは 5〜 35重量%含有する。 また、 (b) 成分は 0. 5〜 1 0重量。 /0、 好ましくは 0. 5〜5重量%である。 さらに、 (a) 成分 Z (b) 成分を 80/20-99/1, 特に 85/1 5〜95 1の 重量比で含有することが柔軟効果及び防臭効果の点から好ましい。 The softener composition of the present invention preferably contains the component (a) in an amount of 3 to 50% by weight, more preferably 3 to 40% by weight. /. And particularly preferably 5 to 35% by weight. The component (b) weighs 0.5 to 10 weight. / 0 , preferably 0.5-5% by weight. Further, it is preferred from the viewpoint of the softening effect and the deodorizing effect that the component (a) contains the component Z (b) in a weight ratio of 80 / 20-99 / 1, particularly 85/15 to 951.
本発明で (c) 成分を用いる場合には (c) 成分を 0. 1〜1 5重量。/。、 好ま しくは 1〜1 5重量。 /。、 特に好ましくは 3〜 1 0重量。 /0含有する。 また、 衣料の 風合レ、及び消臭効果の点から ( c ) / (a) が重量比で 1 Z 30〜 1 Z 1、 好ま しくは 1Z1 0〜1/1が望ましい。 また、 本発明で (d) 成分を用いる場合に は (d) 成分を好ましくは 0. 1〜1 5重量。/。、 より好ましくは 0. 2〜1 0重 量。 /0であり、 ( a ) / (d) が重量比で 50Zl〜2Zl、 好ましくは 30Zl〜 2/1 , より好ましくは 2 OZl〜2Ζ1·が衣料の風合い及び消臭効果の点から 望ましい。 When the component (c) is used in the present invention, the component (c) is used in an amount of 0.1 to 15% by weight. /. , Preferably 1 to 15 weight. /. Particularly preferred is 3 to 10 weight. / 0 contained. Further, (c) / (a) is desirably 1Z30 to 1Z1, preferably 1Z10 0 to 1/1 by weight in terms of the feeling of clothing and the deodorizing effect. When the component (d) is used in the present invention, the component (d) is preferably 0.1 to 15 weight. /. And more preferably 0.2 to 10 weights. / 0 , and (a) / (d) is 50Zl to 2Zl, preferably 30Zl to 2/1, more preferably 2 OZl to 2Ζ1 ·, is desirable from the viewpoint of the texture and deodorizing effect of clothing.
本発明の柔軟剤組成物は、 少なくとも (a) 成分と (c) 成分又は (b) 成分 並びに (d) 成分を水で稀釈した水溶液の形態が好ましい。 使用する水は蒸留水 又はイオン交換水が好ましい。 また、 水は組成物中に 40〜90重量%、 より好 ましくは 50〜 85重量%、 特に好ましくは 60〜 85重量%配合することが貯 蔵安定性の点で望ましい。  The softener composition of the present invention is preferably in the form of an aqueous solution obtained by diluting at least the component (a) and the component (c) or the component (b) and the component (d) with water. The water used is preferably distilled water or ion-exchanged water. Further, it is desirable from the viewpoint of storage stability that water is contained in the composition in an amount of 40 to 90% by weight, more preferably 50 to 85% by weight, and particularly preferably 60 to 85% by weight.
さらに、 本発明の組成物は、 消臭効果及び貯蔵安定性の点から、 20°Cにおけ る pHを 1〜6、 更に 2〜5、 特に 2. 5〜4に調整することが好ましい。 本発明では貯蔵安定性の点から上記 (a)、 (b)、 (c) 及び (d) 成分に加え てさらに (e) 非イオン界面活性剤を配合することが好ましい。 非イオン界面活 性剤としては炭素数 8〜 20のアルキル基またはアルケニル基を 1つ以上有する ポリオキシエチレンアルキルエーテルが好ましく、 特に一般式 (6) の非イオン 界面活性剤が良好である。  Further, the composition of the present invention is preferably adjusted to have a pH at 20 ° C. of 1 to 6, more preferably 2 to 5, particularly 2.5 to 4, from the viewpoint of deodorizing effect and storage stability. In the present invention, from the viewpoint of storage stability, it is preferable to further blend (e) a nonionic surfactant in addition to the components (a), (b), (c) and (d). As the nonionic surfactant, a polyoxyethylene alkyl ether having at least one alkyl or alkenyl group having 8 to 20 carbon atoms is preferable, and a nonionic surfactant represented by the general formula (6) is particularly preferable.
R2" -U-[(R250)p-H]q (6) R 2 "-U - [(R 25 0) pH] q (6)
〔式中、 R24は、 炭素数 10〜1 8、 好ましくは 1 2〜1 8のアルキル基又はァ ルケニル基であり、 R 25は炭素数 2又は 3のアルキレン基であり、 好ましくは エチレン基である。 pは 2〜100、 好ましくは 5〜80、 更に好ましくは 1〇 〜80、 特に好ましくは 20〜60、 の数を示す。 Uは一 O—、 一 CON—又は —N—であり、 Uが—〇一の場合は qは 1であり、 Uが一 CON—又は一 N—の 場合は qは 2である。〕。 Wherein R 24 is an alkyl group or an alkenyl group having 10 to 18 carbon atoms, preferably 12 to 18 carbon atoms, and R 25 is an alkylene group having 2 or 3 carbon atoms, preferably an ethylene group. It is. p represents a number of 2 to 100, preferably 5 to 80, more preferably 1 to 80, and particularly preferably 20 to 60. U is one O—, one CON— or —N—, q is 1 when U is —〇 one, and q is two when U is one CON— or one N—. ].
一般式 (6) の化合物の具体例として以下の化合物を挙げることができる。 R2 -0-(C2H,0)r-H Specific examples of the compound represented by the general formula (6) include the following compounds. R 2 -0- (C 2 H, 0) rH
〔式中、 R24は前記の意味を示す。 rは、 (c) 成分を含む場合は 8〜1 00、 ( d ) 成分を含む場合は 5〜 100、 好ましくは 1 0〜 80、 更に好ましくは 2 0〜80の数である。〕 R2 -0-(C2H40) s (C3H60)t-H [Wherein, R 24 has the meaning described above. r is 8 to 100 when the component (c) is included, When the component (d) is contained, the number is 5 to 100, preferably 10 to 80, and more preferably 20 to 80. ] R 2 -0- (C 2 H 4 0) s (C 3 H 6 0) tH
〔式中、 R24は前記の意味を示す。 s及び tはそれぞれ独立に 2〜40、 好まし くは 5〜 40の数であり、 好ましくは s + tは 1 0〜 80の数であり、 エチレン ォキシドとプロピレンォキシドはランダムあるいはブロック付加体であってもよ い。〕
Figure imgf000010_0001
[Wherein, R 24 has the meaning described above. s and t are each independently 2 to 40, preferably 5 to 40, preferably s + t is a number from 10 to 80, and ethylene oxide and propylene oxide are random or block adducts. It may be. ]
Figure imgf000010_0001
(C2H40)u— H (C 2 H 4 0) u — H
R24-N R 24 -N
ヽ (C2H40)v—H ヽ (C 2 H 4 0) v —H
[式中 R 24は前記の意味を示す。 u及び Vの合計は、 (c) 成分を含む場合は 5~1 00、 (d) 成分を含む場合は 10〜80、 好ましくは 5〜80の数である。 ] 上記非イオン界面活性剤の配合量は安定性の点から 0. 5〜 1 0重量%、 好まし くは:!〜 8重量%である。 本発明では繊維製品の風合いを向上させる目的で ( f ) 炭素数 8〜22の脂肪 酸又はその塩を 0. 1〜5重量%、 特に 0. 5〜3重量%が好ましい。 脂肪酸又はその塩類としては力プリル酸、 力プリン酸、 ラウリン酸、 ミリスチ ン酸、 ノ ノレミチン酸、 ステアリン酸、 ォレイン酸、 あるいはこれらの混合物であ り、 特にラウリン酸、 ステアリン酸、 ォレイン酸から選ばれる 1種以上が良好で ある。 また、 ヤシ油、 パーム油、 パーム核油、 牛脂から誘導されるアルキル組成 を有する脂肪酸も好ましい。 本発明では、 貯蔵安定性の点から、 炭素数 8〜22の飽和又は不飽和脂肪酸と 多価アルコールとのエステル化合物を組成物中 0. 1〜1 0重量%、 特に 0. 5 〜 5重量%配合することが好ましい。 エステル化合物としては、 トリグリセライ ド、 ジグリセライ ド、 モノダリセライ ド、 ペンタエリスリ トールのモノ、 ジ、 ト リエステル、 ソルビタンエステルが好ましレ、。 [Wherein R 24 has the above-mentioned meaning. The sum of u and V is 5 to 100 when the component (c) is included, 10 to 80 when the component (d) is included, and preferably 5 to 80. ] The amount of the nonionic surfactant is 0.5 to 10% by weight from the viewpoint of stability, preferably:! ~ 8% by weight. In the present invention, (f) a fatty acid having 8 to 22 carbon atoms or a salt thereof is preferably 0.1 to 5% by weight, particularly preferably 0.5 to 3% by weight for the purpose of improving the texture of the textile product. Fatty acids or salts thereof are power prillic acid, power pric acid, lauric acid, myristic acid, nonoremitic acid, stearic acid, oleic acid, or a mixture thereof, particularly selected from lauric acid, stearic acid, and oleic acid. One or more types are good. Further, fatty acids having an alkyl composition derived from coconut oil, palm oil, palm kernel oil, and tallow are also preferable. In the present invention, from the viewpoint of storage stability, an ester compound of a saturated or unsaturated fatty acid having 8 to 22 carbon atoms and a polyhydric alcohol is contained in the composition in an amount of 0.1 to 10% by weight, especially 0.5 to 10% by weight. It is preferable that the content be 5 to 5% by weight. As the ester compound, triglyceride, diglyceride, monodalicelide, and pentaerythritol mono, di, triester, and sorbitan esters are preferred.
本発明では、 無機塩、 例えば塩化カルシウムなどを 0〜1 000 p pm、 好ま しくは:!〜 1 0 00 p pm、 更に好ましくは 1 0〜500 p p m添加することが 貯蔵安定性の点で望ましい。 但し、 脂肪酸塩類などの界面活性剤にはナトリウム 塩や力リゥム塩が含まれているが、 このような界面活性剤の使用によって組成物 に混入する無機塩は上記制限を受けるものではない。  In the present invention, an inorganic salt, for example, calcium chloride, is used at 0 to 1 000 ppm, preferably:! ~ 100 ppm, more preferably from 10 to 500 ppm is desirable from the viewpoint of storage stability. However, surfactants such as fatty acid salts include sodium salts and magnesium salts, but inorganic salts mixed into the composition by use of such surfactants are not subject to the above restrictions.
さらに本発明では、 エタノール、 イソプロパノール、 グリセリン、 エチレング リコ一ノレ、 プロピレンダリコーノレ、 ジエチレングリコーノレ、 ジプロピレンダリコ ール及びポリオキシエチレンフエニルエーテルから選ばれる溶媒成分を配合する ことが貯蔵安定性の点から好ましい。 これら溶媒成分は、 組成物中に 0〜2 0重 量%、 更に 0. 1〜 20重量%、 特に 0. 5〜 1 0重量%配合することが好まし レ、。 なお、 エタノールを使用する場合は、 ポリオキシエチレンアルキルエーテル 硫酸塩変性エタノ一ルゃ 8—ァセチル化蔗糖変性エタノールを使用することが望 ましい。  Furthermore, in the present invention, storage stability can be achieved by blending a solvent component selected from ethanol, isopropanol, glycerin, ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, and polyoxyethylene phenyl ether. It is preferable from the viewpoint of properties. These solvent components are preferably incorporated in the composition in an amount of 0 to 20% by weight, more preferably 0.1 to 20% by weight, and particularly preferably 0.5 to 10% by weight. When ethanol is used, it is preferable to use polyoxyethylene alkyl ether sulfate-modified ethanol 8- 8-acetylated sucrose-modified ethanol.
本発明の柔軟剤組成物には、通常繊維処理剤に配合されるシリコーン、香料(特 に好ましくは特開平 8— 1 1 3 8 7号公報記載の成分 (c) 及び (d) にて示さ れた香気成分の組み合わせ) あるいは色素等の成分を配合しても差し支えない。 実施例  The softener composition of the present invention contains a silicone and a fragrance (particularly preferably those represented by components (c) and (d) described in Japanese Patent Application Laid-Open No. Or a combination of components such as pigments. Example
く配合成分〉 Ku ingredients>
以下に実施例に用いた成分を示す。  The components used in the examples are shown below.
(a - 1)
Figure imgf000012_0001
(a-1)
Figure imgf000012_0001
R ;炭素数 1 8及び 1 6が混合した飽和アルキル基 (炭素数 1 8 :炭素数 1 6  R: a saturated alkyl group in which C18 and C16 are mixed (C18: C16
= 6 0/4 0 重量比) = 6 0/4 0 weight ratio)
(a - 2) (a-2)
RCOOCつ \ CH3 RCOOC tsu \ CH 3
cr  cr
RCOOC2H4'/" CH2CH2OH RCOOC 2 H 4 ' / "CH 2 CH 2 OH
R ;炭素数 1 8及び 1 6が混合した飽和アルキル基 (炭素数 1 8 :炭素数 1 6  R: a saturated alkyl group in which C18 and C16 are mixed (C18: C16
= 6 0/4 0 重量比) = 6 0/4 0 weight ratio)
(a— 3) (a— 3)
RCOOC2 , CH3 RCOOC 2 , CH 3
ノ\ ci- ノ \ ci-
RCONHC3¾ CH3 RCONHC 3 ¾ CH 3
R ;炭素数 1 7及び 1 5が混合した飽和アルキル基 (炭素数 1 7 :炭素数 1 5  R: a saturated alkyl group in which C17 and C15 are mixed (C17: C15
= 6 0/4 0 重量比) = 6 0/4 0 weight ratio)
(a— 4)
Figure imgf000012_0002
(a— 4)
Figure imgf000012_0002
R ;炭素数 1 7及び 1 5が混合した飽和アルキル基 (炭素数 1 7 :炭素数 1 5  R: a saturated alkyl group in which C17 and C15 are mixed (C17: C15
= 6 0/4 0 重量比) = 6 0/4 0 weight ratio)
(a— 5) ジォレオイルヒ ドロキシェチルジメチルアンモニゥムメチルサルフエ ート (a—5) Dioleoyl hydroxethyl dimethyl ammonium methyl sulfate
(a— 6) (a— 6)
RCOOCつ H4 RCOOC2H4
Figure imgf000012_0003
RCOOC H 4 RCOOC 2 H 4
Figure imgf000012_0003
R ;炭素数 1 7及び 1 5が混合した飽和アルキル基 (炭素数 1 7 :炭素数 1 5 = 60/40 重量比) (a' - l) ジォ ニゥムクロリ ド R: a saturated alkyl group in which C17 and C15 are mixed (C17: C15 = 60/40 weight ratio) (a '-l) dionium chloride
(b - 1) (b-1)
HOC2¾i、 CH3 HOC 2 ¾i, CH 3
: N C1  : N C1
RCONHC3H6z Η3 RCONHC 3 H6z Η 3
R ;炭素数 18および 1 6が混合した飽和アルキル基 (炭素数 18 Z炭素数 1 6 = 60 Z 40 重量比)  R: saturated alkyl group in which C18 and C16 are mixed (C18ZC16 = 60Z40 weight ratio)
(b - 2)
Figure imgf000013_0001
(b-2)
Figure imgf000013_0001
R ;炭素数 1 7および 1 5が混合した飽和アルキノレ基 (炭素数 1 7 /炭素数 1 5 = 60 Z 4◦ 重量比 重量比)  R: Saturated alkynole group in which 17 and 15 carbon atoms are mixed (17 carbon atoms / 15 carbon atoms = 60 Z 4◦ weight ratio weight ratio)
(c一 1)
Figure imgf000013_0002
(c-1)
Figure imgf000013_0002
(c-2)
Figure imgf000013_0003
(c-2)
Figure imgf000013_0003
(c -3)  (c -3)
Ci H. ■N z Ci H. ■ N z
(d— 1) ジデシルジメチルアンモニゥムクロリ ド (d-1) Didecyldimethylammonium chloride
(e— 1) 炭素数 12の飽和アルコールにエチレンォキサイ ドを平均 2 1モル付 加させたもの (e-1) An average of 21 moles of ethylene oxide added to a saturated alcohol having 12 carbon atoms.
(e— 2) ラウリン酸のジエタノールアミ ドにエチレンォキシドを平均 20モル 付加させたもの (e-2) Average of 20 moles of ethylene oxide in lauric acid diethanolamide Added
(f 一 1) ルナック S— 50 (ステアリン酸、 花王 (株) 製)  (f-1) Lunac S-50 (stearic acid, manufactured by Kao Corporation)
(f 一 2) ラウリン酸  (f-1 2) Lauric acid
(f 一 3) ミリスチン酸  (f-1 3) myristic acid
( f - 4) パルミチン酸  (f-4) palmitic acid
( g— 1 ) ェキセル 1 50 〔ステアリン酸モノ、 ジ、 トリグリセリ ド混合物 (モ ノ : ジ: トリ = 60 : 35 : 5 ) 花王 (株) 製〕 ( g -1) exel 150 [Mono, di, triglyceride mixture (mono: di: tri = 60: 35: 5) manufactured by Kao Corporation]
(g— 2) 塩化カルシウム  (g-2) Calcium chloride
(g - 3) エチレングリコール  (g-3) Ethylene glycol
(h- 1) 色素 (ァシッ ドブルー 9 )  (h-1) Dye (acid blue 9)
(h— 2)香料〔へキシルシンナミックアルデヒ ド(1 8)、ネロリンャラャラ(4)、 トリシクロデセニルアセテート (4)、 ベンジルアセテート (1 0)、 ムスクケト ン (5)、 ァニシルアセトン (2)、 サンダルマイソールコア (2)、 アルデヒ ド C 14ピーチ ( 1 )、 リナロール (18 )、 ジヒ ドロキシミルセノ一ノレ ( 8 )、 ボルネ オール (4)、 セドローノレ (4)、 ムゴーノレ (5)、 ベンジルアルコール (5)、 ジ プロピレンダリコール (1 0) の混合物:カツコ内は香料中の重量0 /0(h-2) Fragrance [Hexylcinnamic aldehyde (18), nerolinalalara (4), tricyclodecenyl acetate (4), benzyl acetate (10), musketone (5), anisylacetone (2) , Sandal Mysore Core (2), Aldehyde C14 Peach (1), Linalool (18), Dihydroxymilsenomono (8), Borneol (4), Cedro Nole (4), Mgonole (5), Benzyl Alcohol (5) ), dipropylene da recall (1 0) mixture of: weight 0/0 in Katsuko during perfumes]
(h— 3) シリ コーン (東芝シリ コーン製、 TSA 730)。  (h-3) Silicone (Toshiba Silicone, TSA 730).
実施例 1  Example 1
上記化合物を用いて表 1に示す柔軟剤組成物を調製した (本発明品 1〜 6及び 比較品 1〜 3)。セーター(コットン 100%) 2枚を市販の弱アルカリ性洗剤(花 王製アタック) を用いて洗濯機で洗浄した (東芝製 2槽式洗濯機 VH— 360 S 1、 洗剤濃度 0. 0667重量。/。、 水道水 30 L使用、 水温 20°C, 1 0分間)。 その後洗浄液を排出し、 1分間脱水後、 30 Lの水道水を注水して 5分間すすぎ を行い、 排水後 1分間脱水を行った。 その後再度 30 Lの水道水を注水した後、 表 1の柔軟剤組成物 5 gを添カ卩し 5分間攪拌した。 その後、 脱水し、 湿度 70 %、 2 5°Cの恒温室で 1 2時間乾燥した。 The softener compositions shown in Table 1 were prepared using the above compounds (Products 1 to 6 of the present invention and Comparative products 1 to 3). Two sweaters (100% cotton) were washed in a washing machine using a commercially available weak alkaline detergent (Kao Attack) (Toshiba 2-tub washing machine VH-360 S1, detergent concentration 0.0667 weight / , 30 L of tap water, water temperature 20 ° C, 10 minutes). After that, the washing liquid was drained, and after dehydration for 1 minute, 30 L of tap water was injected, rinsed for 5 minutes, and dewatered for 1 minute after drainage. After injecting 30 L of tap water again, 5 g of the softener composition shown in Table 1 was added to the mixture and stirred for 5 minutes. Then, it was dehydrated and dried for 12 hours in a constant temperature room at 70% humidity and 25 ° C.
(柔軟性能の評価)  (Evaluation of flexible performance)
表 1の柔軟剤組成物及び対応する組成物から抗菌成分 〔(c) 成分又は (d) 成 分〕 を除いた組成物を用いて上記柔軟処理を行い、 1 0人のパネラーに 1対比較 で下記の基準で評価し、 平均点を求めた。  The above softening treatment was performed using the softener composition shown in Table 1 and the corresponding composition excluding the antibacterial component [(c) component or (d) component], and 10 panelists were compared with each other. The evaluation was performed according to the following criteria, and the average score was obtained.
(c) 又は (d) 成分の有る方が柔らかく仕上がる… + 1  (c) or (d) The one with the component is finished softer ... + 1
(c) 又は (d) 成分の有り無しで仕上がりに差はない…… 0  (c) or (d) There is no difference in the finish with or without the ingredients ... 0
(c) 又は (d) 成分の無い方が柔らかく仕上がる……一 1。  (c) or (d) The one without the component is softer and finished.
(臭い評価)  (Smell evaluation)
恒温室で乾燥させた衣料の臭いと、 それら衣料を 20代男性 5人に 1 2時間着 用させた後の衣料の臭いを、 それぞれ 1 0人のパネラー (30代男性 1 0人) に より下記の基準で判定し、 それぞれ平均点を求めた。  The smell of the clothes dried in the constant temperature room and the smell of the clothes after putting them on five men in their twenties for 12 hours was determined by 10 panelists (10 men in their 30s). Judgment was made according to the following criteria, and the average score was determined for each.
ほとんど臭いを感じない…… 0 Almost no smell ... 0
かすかに臭いを感じるが気にならない程度である…… 1 Feel the smell faintly but don't mind ... 1
臭いがする ··…- 2 Smells ... 2
顕著に臭いがする…… 3 It smells noticeably ... 3
表 1 table 1
Figure imgf000016_0001
Figure imgf000016_0001
* p Hは N/10硫酸水溶液又は NZlO水酸化ナトリゥム水溶液により調整した 実施例 2 * pH was adjusted with N / 10 sulfuric acid aqueous solution or NZlO sodium hydroxide aqueous solution Example 2
表 2に記載の組成の柔軟剤組成物 (本発明品 7 1 1 ) を実施例 1と同様にし て調製した。 なお、 香料は表 3の組成のもの 1 0 0重量部に対しジプロピレング リ コ一ノレ 1 0重量部を混合したものを用いた。 それらについて実施例 1同様に評 価したところ、 何れも優れた臭い抑制効果と柔軟性能が認められた。 表 2 A softener composition having the composition shown in Table 2 (product 7111 of the present invention) was prepared in the same manner as in Example 1. The fragrance used was a mixture of 100 parts by weight of the composition shown in Table 3 and 10 parts by weight of dipropylene glycol. When they were evaluated in the same manner as in Example 1, excellent odor control effect and softness were recognized in all cases. Table 2
Figure imgf000017_0001
Figure imgf000017_0001
* p Hは NZ10硫酸水溶液又は N/10水酸化ナトリゥム水溶液により調整した c * P H was adjusted by NZ10 aqueous sulfuric acid or N / 10 Natoriumu hydroxide solution c
表 3 Table 3
^ &枓成分 {M vo) 科 1 杳枓 杳抖 4 杳抖 5 へキンノレンンナ ックァノレァヒ ト 0 0 1 3 0 0 才、ロリンャラャラ 0 0 3 0 0 ― _ - トリンクロアセニノレアセァート 0 0 3 0 0 ベンンノレ セァ ト 0 0 7 0 0 ムスクケトン 0 0 3 0 0 ァニシノレアで トン 0 0 1 0 0 サンダノレマイソーノレコア 0 0 1 0 0 ァノレデヒ ド C 1 4ピ一テ 0 0 1 0 0 メチノレイオノン一ガンマ 7 0 0 3 0 ィソィ一ス一パー 7 0 0 3 0 テンタローム 1 4 0 0 7 0 ^ & 枓 component (M vo) Family 1 枓 枓 抖 4 5 抖 5 へ 1 ロ 0 0 1 3 0 0 years old, Lorinjala Lara 0 0 3 0 0 ― _- Bennoure Sat 0 0 7 0 0 Musk Ketone 0 0 3 0 0 Tons at Vanishinorea 0 0 1 0 0 Sandanore Maisone Recoa 0 0 1 0 0 0 0 3 0 Issuer 7 7 0 0 3 0 Tentarom 1 4 0 0 7 0
4— tーブチノレンクロ^ "シノレア ト 1 4 0 0 7 0 リ リアール 2 0 0 0 1 0 0 へソォナ—ノレ 3 0 0 2 0 クマリン 3 0 0 1 0 アン:、 'ロキサン 1 0 0 0 0 ターピニノレアセテート 0 1 2 0 0 2 0 セドリノレァセテ ト 0 8 0 0 1 3 リラ一ル 0 8 0 0 1 3 ノヽ0—ノレライ ド 0 4 0 0 7 サンダノレシンス 0 4 0 0 7 フェニノレアセ トセノレデヒ ド 5 0 % P E A 0 0 0 0 1 テノレデヒ ド C 1 2 MN A 0 0 0 0 1 シンナミノレシンナメ一ト 0 2 0 0 3 ベンシノレイソオイケノーノレ 0 2 0 0 3 リナ Π—ル 0 0 0 0 1 3 ジヒ ドロキシミノレセノ—ノレ 0 0 0 0 7 ボノレネ才ーノレ 0 0 0 0 3 セ ドロール 0 0 0 0 3 ムゴール 0 0 0 0 3 ベンジノレアノレコーノレ 0 0 0 0 3 フエニノレエチノレアノレコーノレ 1 2 0 2 9 0 0 シ卜ロネ Π—ル 6 0 1 3 0 0 ターピ.ネオ ノレ 6 0 1 3 0 0 フエニノレエチノレンメチノレカノレビノ——ノレ 3 0 7 0 0 スナフリノレ/ノレコ^ ~ノレ 2 0 3 0 0 ノノ"ノ" ~、' 、ノノ ノ 1 ;1 9 π υ υ π υ4—t-Buchinorenkuro ^ “Sinoreto 1 4 0 0 7 0 Lilyar 2 0 0 0 1 0 0 Hesona-Nore 3 0 0 2 0 Coumarin 3 0 0 1 0 An :, 'Loxane 1 0 0 0 0 Tarpi Nino Les acetate 0 1 2 0 0 2 0 Sedorinoreasete DOO 0 8 0 0 1 3 lira Ichiru 0 8 0 0 1 3 Nono 0 - Norerai de 0 4 0 0 7 Sandanoreshinsu 0 4 0 0 7 Feninorease Tosenoredehi de 5 0% PEA 0 0 0 0 1 Tenored C 1 2 MN A 0 0 0 0 1 Cinnaminorecin Cinnament 0 2 0 0 3 Bencinoreisoenanoen 0 2 0 0 3 Lina Pole 0 0 0 0 1 3 Dihydro Kisminoreseno-Nore 0 0 0 0 7 Bonolene Nono 0 0 0 0 3 Cedorol 0 0 0 0 3 Mugol 0 0 0 0 3 Benzinorea Noreconore 0 0 0 0 3 Fueninole Etinorea Noreno 1 2 0 2 9 0 0 Cytrone 6 0 1 3 0 0 Tarpi Neo Neo 6 0 1 3 0 0 Phenoinoletinolene Mechinorekanorebino-Nore 3 0 7 0 0 Snafle / Noreco ~ ~ Nore 2 0 3 0 0 Nono "No" ~, ', Nono 1; 1 9 π υ υ π υ
1—メント—ノレ 0 2 4 0 2 7 0 ゲラニオール 0 1 2 0 1 3 0 ジヒ .ドロミノレセノ——ノレ 0 1 2 0 1 3 0 フエ二ノレへキサノーノレ 0 6 〇 7 0 ジメチルベンジルカノレビノール 0 6 0 7 0 合計 (重量。/。) 1 0 0 1 0 0 1 0 0 1 0 0 1 0 0 実施例 3 1-mento-nore 0 2 4 0 2 7 0 geraniol 0 1 2 0 1 3 0 dihidro-dominoreseno-nore 0 1 2 0 1 3 0 feninolenohexanonore 0 6 〇 7 0 dimethylbenzylcanolevinol 0 6 0 7 0 Total (weight./.) 1 0 0 1 0 0 1 0 0 1 0 0 1 0 0 Example 3
上記化合物を用いて表 4に示す柔軟剤組成物を調製した。 ワイシャッ (木綿 1 00 %) 5枚及びタオル (木綿 100 %) 5枚 (衣料の全重量 1. 5 k g) を巿 販の弱アルカリ性洗剤 (花王製アタック) を用いて洗濯機で洗浄した (東芝製 2 槽式洗濯機 VH_ 360 S 1、 洗剤濃度 0. 0667重量%、 水道水 30 L使用、 水温 20°G、 1 0分間)。 その後、 洗浄液を排出し、 1分間脱水後、 30 Lの水道 水を注水して 5分間すすぎを行い、 排水後 1分間脱水を行った。 その後、 再度 3 0 Lの水道水を注水した後、 表 1の組成物 7 m 1を添加し 5分間攪拌した。 その 後、 脱水し自然乾燥した。  Using the above compounds, softener compositions shown in Table 4 were prepared. Five pieces of Wishash (100% cotton) and five pieces of towel (100% cotton) (total weight of clothing: 1.5 kg) were washed in a washing machine using a commercially available weak alkaline detergent (Kao Attack) (Toshiba 2-tub washing machine VH_360 S1, detergent concentration 0.0667% by weight, tap water 30L used, water temperature 20 ° G, 10 minutes). After that, the washing solution was drained, and after dehydration for 1 minute, 30 L of tap water was injected, rinsed for 5 minutes, and dewatered for 1 minute after drainage. Thereafter, 30 L of tap water was injected again, and then 7 ml of the composition shown in Table 1 was added thereto, followed by stirring for 5 minutes. After that, it was dehydrated and air-dried.
(消臭効果の評価)  (Evaluation of deodorant effect)
上記の処理をしたワイシャツを 20代男性 5人に 1 2時間着用してもらい、 着 用後のワイシャツから発生する汗由来の臭いを 10人のパネラー (30代男性 1 0人) により下記の基準で判定し、 平均点を求めた。 平均点が 0. 8未満を〇、 0. 8以上 1. 2未満を口、 1. 2以上 1. 7未満を△、 1. 7以上を Xとして 評価し表 1に示した。  Five men in their twenties wear the treated shirt for 12 hours, and the sweat-derived odor generated by the shirt after wearing is judged by 10 panelists (10 men in their 30s) according to the following criteria: The average score was determined. Table 1 shows the average score of less than 0.8 as “〇”, 0.8 or more and less than 1.2 as mouth, 1.2 or more and less than 1.7 as “△”, and 1.7 or more as “X”.
ほとんど臭いを感じない…… 0  Almost no smell ... 0
かすかに臭いを感じるが気にならない程度である…… 1  Feel the smell faintly but don't mind ... 1
臭いがする…… 2  It smells ... 2
顕著に臭いがする…… 3  It smells noticeably ... 3
(柔軟性評価)  (Flexibility evaluation)
上記の処理をしたタオルと表 4の組成物を用いずに同様の処理を行ったタオル (対照) を 10人のパネラー (30代男性 1 0人) により下記の基準で判定し、 平均点を求めた。 平均点が 2以上を〇、 1以上 1. 5未満を口、 0. 5以上 1未 満を△、 0. 5未満を Xとして評価し表 1に示した。 + 3 :対照より非常に柔らかい + 2 ;対照より柔らかい + 1 ;対照よりやや柔らかい 0 ;対照と同等である 10 panelists (10 males in their 30s) judged the towels treated as described above and the towels (control) treated in the same manner without using the composition in Table 4 according to the following criteria, and the average score was calculated. I asked. Table 1 shows the results when the average score was 2 or more, rated as 〇, 1 or more, but less than 1.5, as mouth, 0.5 or more, but less than 1 as △, and X, less than 0.5. +3: very soft than the control + 2; softer than the control + 1; slightly softer than the control 0; equivalent to the control
表 4 Table 4
Figure imgf000021_0001
Figure imgf000021_0001
* p H調製は、 10 N塩酸水溶液及び 0 N水酸化ナトリゥム水溶液  * pH is adjusted by 10 N hydrochloric acid aqueous solution and 0 N sodium hydroxide aqueous solution.

Claims

請求の範囲 The scope of the claims
1、 (a ) 下記一般式 (1 ) の 4級アンモニゥム化合物、 及び (b) 下記一般 式(2) の 4級アンモニゥム化合物を含有し、 さらに下記(c )成分又は下記(d) 成分から選ばれる化合物を含有する柔軟剤組成物。 Z- ( 1 )1, containing (a) a quaternary ammonium compound of the following general formula (1), and (b) a quaternary ammonium compound of the following general formula (2), and further selected from the following component (c) or the following component (d) Softener composition containing the compound to be prepared. Z- (1)
Figure imgf000022_0001
Figure imgf000022_0001
〔式中、 R R2は、 それぞれ独立に、 炭素数 1 2〜2 2のアルキル基又はアル ケニル基を示し、 X、 Yは、 それぞれ独立に、 一 COO—、 一 CONR 7—、 一 OCO—、 _NR7CO—であり、 少なくともいずれか一方は一 COO—、 一 O CO—である。 ここで R7は水素原子、 炭素数 1〜 3のアルキル基又はヒ ドロキ シアルキル基を示す。 R3、 R4は、 それぞれ独立に、 炭素数 1〜5のアルキレン 基であり、 R5、 R6は炭素数 1〜3のアルキル基もしくはヒ ドロキシアルキル基 又は R 1— X— R3—であり、 Z-は陰イオン基である。〕
Figure imgf000022_0002
Wherein, RR 2 each independently represents a number 1 2-2 2 alkyl group or an alkenyl group having a carbon, X, Y are each independently one COO-, One CONR 7 - one OCO- , _NR 7 CO—, at least one of which is one COO— and one O CO—. Here, R 7 represents a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group. R 3 and R 4 are each independently an alkylene group having 1 to 5 carbon atoms, and R 5 and R 6 are an alkyl group or a hydroxyalkyl group having 1 to 3 carbon atoms or R 1 — X—R 3 — And Z- is an anionic group. ]
Figure imgf000022_0002
[式中、 R8は炭素数 1 2〜2 2のアルキル基又はアルケニル基を示し、 Wは—C ◦ 0—、 一 CONR7—、 一 OCO—、 一 NR7 C〇一から選ばれる基である。 こ こで R7は水素原子、 炭素数 1〜 3のアルキル基又はヒ ドロキシアルキル基、 好 ましくは水素原子である。 また、 R 9は炭素数 1〜 5のアルキレン基であり、 R ' °、 R 11は炭素数 1〜 3のアルキル基又はヒ ドロキシアルキル基であり、 R 1 2は 炭素数 1〜 3のアルキル基又は一 R26—〇Hである。 ここで R26は炭素数 1〜 5 のアルキレン基である。 Z—は陰イオン基である。 ] [Wherein, R 8 represents an alkyl group or an alkenyl group having 12 to 22 carbon atoms, and W represents a group selected from —C ◦ 0—, one CONR 7 —, one OCO—, and one NR 7 C}. It is. Here, R 7 is a hydrogen atom, an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group, preferably a hydrogen atom. Also, R 9 is an alkylene group having 5 to several carbon atoms, R '°, R 11 is an alkyl group or hydroxycarboxylic alkyl group 1-3 carbon atoms, R 1 2 is of 1-3 carbon atoms An alkyl group or one R 26 —〇H. Here, R 26 is an alkylene group having 1 to 5 carbon atoms. Z— is an anionic group. ]
( c ) 下記一般式 (3) の化合物及び/又は一般式 (4) の化合物を 0. 1〜 1
Figure imgf000023_0001
(c) The compound of the following general formula (3) and / or the compound of the general formula (4) is 0.1 to 1
Figure imgf000023_0001
〔式中 R13、 R18は、 それぞれ独立に、 炭素数 5〜1 9のアルキル基又はアルケ ニル基であり、 R14、 R15は、 それぞれ独立に、 炭素数 1〜3のアルキル基又は ヒ ドロキシアルキル基である。 Tは一 CO〇_、 _〇C〇一、 一 CONH—、 - NHCO—、
Figure imgf000023_0002
Wherein R 13 and R 18 are each independently an alkyl group having 5 to 19 carbon atoms or an alkenyl group, and R 14 and R 15 are each independently an alkyl group having 1 to 3 carbon atoms or It is a hydroxyalkyl group. T is one CO〇_, _〇C〇 one, one CONH—,-NHCO—,
Figure imgf000023_0002
あるいは連結手である。 R 16は炭素数 1〜3のアルキレン基であり、 R 17は炭素 数 1〜6のアルキレン基又は一(0_R19)n—である。 ここで R 19はエチレン基 又はプロピレン基であり、 nは 1〜10の数である。 W—は陰イオン基である。〕Or a connecting hand. R 16 is an alkylene group having 1 to 3 carbon atoms, and R 17 is an alkylene group having 1 to 6 carbon atoms or one (0_R 19 ) n—. Here, R 19 is an ethylene group or a propylene group, and n is a number of 1 to 10. W— is an anionic group. ]
(d) 下記一般式 (5) の化合物を 0. 01〜] W" (5)(d) A compound represented by the following general formula (5) is converted to 0.01-] W "(5)
Figure imgf000023_0003
Figure imgf000023_0003
〔式中、 R2°、 R2\ R22、 R23の 2又は 3個が炭素数 8〜1 2のアルキル基 であり、 残りが炭素数 1〜 3のアルキル基、 炭素数 1〜3のヒ ドロキシアルキル 基又は総炭素数 7〜1 5のァリールアルキル基であり、 Z—は陰イオン基であ る。〕 (In the formula, two or three of R 2 °, R 2 \ R 22 , and R 23 are an alkyl group having 8 to 12 carbon atoms, and the rest is an alkyl group having 1 to 3 carbon atoms, and 1 to 3 carbon atoms. Is a hydroxyalkyl group or an arylalkyl group having a total carbon number of 7 to 15, and Z— is an anionic group. ]
2、 さらに (e) 非イオン界面活性剤を含有する請求項 1記載の柔軟剤組成物。 2. The softener composition according to claim 1, further comprising (e) a nonionic surfactant.
3、 さらに ( f ) 炭素数 8〜22の脂肪酸又はその塩ひ. 1〜5重量%を含有 する請求項 1又は 2記載の柔軟剤組成物。 3. The softener composition according to claim 1, further comprising (f) a fatty acid having 8 to 22 carbon atoms or a salt thereof. 1 to 5% by weight.
PCT/JP2000/007897 1999-11-12 2000-11-09 Softener composition WO2001036737A1 (en)

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EP0022555A1 (en) * 1979-07-12 1981-01-21 Hoechst Aktiengesellschaft Fabric softener
JPH03287867A (en) * 1990-03-30 1991-12-18 Kao Corp Flexibilizing finish
JPH0598571A (en) * 1991-10-04 1993-04-20 Lion Corp Liquid softener composition
JPH09137379A (en) * 1995-11-13 1997-05-27 Kao Corp Softening and finishing agent
JPH1161640A (en) * 1997-08-06 1999-03-05 Nof Corp Softening agent composition

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US5399272A (en) * 1993-12-17 1995-03-21 The Procter & Gamble Company Clear or translucent, concentrated biodgradable quaternary ammonium fabric softener compositions
IL121037A0 (en) * 1997-06-09 1997-11-20 Innoscent Ltd Laundry fabric softener which inhibits bacterial growth and odor formation

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EP0022555A1 (en) * 1979-07-12 1981-01-21 Hoechst Aktiengesellschaft Fabric softener
JPH03287867A (en) * 1990-03-30 1991-12-18 Kao Corp Flexibilizing finish
JPH0598571A (en) * 1991-10-04 1993-04-20 Lion Corp Liquid softener composition
JPH09137379A (en) * 1995-11-13 1997-05-27 Kao Corp Softening and finishing agent
JPH1161640A (en) * 1997-08-06 1999-03-05 Nof Corp Softening agent composition

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See also references of EP1154068A4 *

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ES2260065T3 (en) 2006-11-01
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