JPH0718571A - Softening agent composition - Google Patents

Softening agent composition

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Publication number
JPH0718571A
JPH0718571A JP18705093A JP18705093A JPH0718571A JP H0718571 A JPH0718571 A JP H0718571A JP 18705093 A JP18705093 A JP 18705093A JP 18705093 A JP18705093 A JP 18705093A JP H0718571 A JPH0718571 A JP H0718571A
Authority
JP
Japan
Prior art keywords
long
chain
amine
acid
softening agent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP18705093A
Other languages
Japanese (ja)
Inventor
Seiichi Ota
誠一 太田
Hiroshi Imada
浩 今田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lion Corp
Original Assignee
Lion Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Lion Corp filed Critical Lion Corp
Priority to JP18705093A priority Critical patent/JPH0718571A/en
Publication of JPH0718571A publication Critical patent/JPH0718571A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain a softening agent composition, containing a specific di-long-chain amine-based softening base and a specified mono-long-chain amine-based softening base, capable of imparting excellent softness to clothes even in the presence of an anionic surfactant carried from a washing cycle therein and suitable for use especially in fully automatic washing machines. CONSTITUTION:This softening agent composition is obtained by blending a di-long-chain amine-based softening base composed of an amine, expressed by formulas I and/or II [R1, R2, R6 and R7 are each a 1-6C alkyl or hydroxyalkyl; R4, R5 and R9 are expressed by formula III or IV (R8, R11 and R12 are each an 8-22C alkyl or alkenyl; R10 is H, OH, a 1-6C alkyl or hydroxyalkyl); (n) and (m) are each an integer of 2-10; (p) is 0 or 1 to 7; (q) is 1-10], having a long-chain amide or a long-chain ester group and neutralized with an inorganic or an organic acid with (B) a mono-long-chain amine-based softening base composed of the amine, expressed by formulas I and/or II [R5 and R9 are especially a (poly)oxyalkylene group], having the long-chain amide or the long-chain ester group and neutralized with the inorganic or organic acid at (97/3) to (40/60) weight ratio of the components (A)/(B). The softening agent composition is capable of imparting softness to clothes and suitable for use in fully automatic washing machines.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、繊維や衣料に柔軟性を
付与するための柔軟剤組成物に関し、特に、洗濯サイク
ルより持ち込まれるアニオン界面活性剤の存在下でも柔
軟性に優れた柔軟剤組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a softener composition for imparting flexibility to fibers and clothing, and particularly to a softener having excellent flexibility even in the presence of an anionic surfactant brought in from a washing cycle. It relates to a composition.

【0002】[0002]

【従来の技術】従来、家庭用柔軟仕上剤として市販され
ている殆どの商品は、ジ(硬化牛脂アルキル)ジメチル
アンモニウムクロライドに代表される第4級アンモニウ
ム塩を主成分として用いている。しかし、近年全自動洗
濯機が普及するにつれ、洗濯サイクルから持ち込まれる
アニオン界面活性剤により柔軟効果が低下する事、及び
環境対応上の観点から微生物等に強い親和力を有する4
級塩は好ましくないと言われる様になつた。これらの事
は、全て4級塩の強いカチオン性に由来する問題である
為、アミン化合物が見直されつつある。しかしながら従
来のメチルジ(硬化牛脂アルキル)アミンの様な長鎖ア
ルキルアミンでは柔軟効果が低く充分ではなかつた。
2. Description of the Related Art Conventionally, most commercial products as household softening agents use a quaternary ammonium salt represented by di (hardened beef tallow alkyl) dimethylammonium chloride as a main component. However, with the spread of fully automatic washing machines in recent years, the anionic surfactant brought in from the washing cycle reduces the softening effect, and has a strong affinity with microorganisms from the viewpoint of environmental friendliness.
Grade salts came to be said to be unfavorable. Since all of these problems are caused by the strong cationic nature of the quaternary salt, amine compounds are being reviewed. However, conventional long-chain alkylamines such as methyldi (hardened tallow alkyl) amine have a low softening effect and are not sufficient.

【0003】[0003]

【発明が解決しようとする課題】本発明は、衣料に対し
て柔軟性を付与すると同時に、全自動洗濯機に最適な柔
軟剤組成物を提供するものである。
DISCLOSURE OF THE INVENTION The present invention provides a softener composition suitable for a fully automatic washing machine, while imparting flexibility to clothes.

【0004】[0004]

【課題を解決するための手段】本発明者らは、鋭意検討
した結果、特定のジ長鎖型アミンとモノ長鎖アミンの併
用により洗濯サイクルから持ち込まれるアニオン界面活
性剤の存在下でも優れた柔軟効果が得られる事を見出し
本発明をなすに至つた。すなわち、本発明の柔軟剤組成
物は、下記(a)及び(b)成分をその配合重量比が
(a)/(b)=97/3〜40/60の範囲となるよ
うに含有することを特徴とする。
Means for Solving the Problems As a result of diligent investigations, the present inventors have found that they are excellent even in the presence of an anionic surfactant brought in from a washing cycle by using a specific dilong-chain amine and a mono-long-chain amine in combination. The inventors have found that a softening effect can be obtained and have completed the present invention. That is, the softener composition of the present invention contains the following components (a) and (b) such that the compounding weight ratio thereof is (a) / (b) = 97/3 to 40/60. Is characterized by.

【0005】(a) 下記化3の一般式(I)及び/又
は(II)で示されるアミンの無機酸又は有機酸の中和物
からなるジ長鎖アミン系柔軟基剤。
(A) A di-long-chain amine-based soft base comprising a neutralized product of an inorganic acid or an organic acid of an amine represented by the following general formula (I) and / or (II).

【化3】 [Chemical 3]

【0006】(b) 下記化4の一般式(III) 及び/
又は(IV)で示されるアミンの無機酸又は有機酸の中和
物からなるモノ長鎖アミン系柔軟基剤
(B) General formula (III) of the following chemical formula 4 and /
Or a mono-long-chain amine-based soft base consisting of a neutralized product of an amine inorganic acid or organic acid represented by (IV)

【化4】 [Chemical 4]

【0007】[0007]

【発明の実施態様】本発明の(a)成分としては、下記
化5の一般式(I)又は(II)で示されるジ長鎖アミン
の無機酸又は有機酸の中和物からなるジ長鎖アミン系柔
軟基剤の1種または2種以上が用いられる。
BEST MODE FOR CARRYING OUT THE INVENTION As the component (a) of the present invention, a di-long chain comprising a neutralized product of an inorganic acid or an organic acid of a di-long chain amine represented by the following general formula (I) or (II) One or more chain amine type soft bases are used.

【0008】[0008]

【化5】 8 ,R11,R12は、炭素数8〜22の直鎖もしくは分
岐鎖アルキル基又はアルケニル基であり、好ましくは炭
素数13〜19の直鎖もしくは分岐鎖アルキル基又はア
ルケニル基である。n,mは、2〜10の整数であり、
好ましくは2〜4の整数である。pは、0又は1〜7の
整数であり、好ましくは0である。qは、1〜10の整
数であり、好ましくは1〜2の整数である。R10は、
H,OHあるいは炭素数1〜6のアルキル基又はヒドロ
キシアルキル基であり、好ましくはHである。
[Chemical 5] R 8, R 11, R 12 is a linear or branched alkyl or alkenyl group having 8 to 22 carbon atoms, preferably a straight-chain or branched alkyl or alkenyl group having 13 to 19 carbon atoms. n and m are integers of 2 to 10,
It is preferably an integer of 2 to 4. p is 0 or an integer of 1 to 7, preferably 0. q is an integer of 1 to 10, preferably an integer of 1 to 2. R 10 is
H, OH or an alkyl group having 1 to 6 carbon atoms or a hydroxyalkyl group, and preferably H.

【0009】(a)成分のジ長鎖アミン系柔軟基剤の一
般式(I)及び(II)の具体例としては、以下の一般式
で示すものが挙げられる。
Specific examples of the general formulas (I) and (II) of the di-long-chain amine-based soft base material as the component (a) include those represented by the following general formula.

【0010】(1) 一般式(I)の具体例:化6、化
7、化8の(I−1)〜(I−9)
(1) Specific examples of the general formula (I): (I-1) to (I-9) in Chemical formula 6, Chemical formula 7, and Chemical formula 8

【化6】 (上記一連の式中、nは2〜10の整数、qは1〜10
の整数を示す。)
[Chemical 6] (In the above series of formulas, n is an integer of 2 to 10 and q is 1 to 10
Indicates an integer. )

【0011】[0011]

【化7】 (上記一連の式中、nは2〜10の整数、qは1〜10
の整数を示す。)
[Chemical 7] (In the above series of formulas, n is an integer of 2 to 10 and q is 1 to 10
Indicates an integer. )

【0012】[0012]

【化8】 (上記一連の式中、nは2〜10の整数を示す。)[Chemical 8] (In the above series of formulas, n represents an integer of 2 to 10.)

【0013】(2) 一般式(II)の具体例:化9,化
10の(II−1)〜(II−8)
(2) Specific examples of the general formula (II): (II-1) to (II-8) of chemical formulas 9 and 10

【化9】 (上記一連の式中、mは2〜10の整数、qは1〜10
の整数を示す。)
[Chemical 9] (In the above series of formulas, m is an integer of 2 to 10, and q is 1 to 10
Indicates an integer. )

【0014】[0014]

【化10】 (上記一連の式中、mは2〜10の整数を示す。)[Chemical 10] (In the above series of formulas, m represents an integer of 2 to 10.)

【0015】前記の一般式(I),(II)中の脂肪酸残
基−COR8 ,−COR11,−COR12は通常、ステア
リン酸、パルミチン酸等の飽和高級脂肪酸、オレイン
酸、エライジン酸、リノール酸、リノレン酸等の不飽和
高級脂肪酸、牛脂、豚脂、パーム油、パーム核油、大豆
油、サフラワー油、ヒマワリ油、オリーブ油等の天然油
脂を分解、精製して得られる脂肪酸から由来するもので
あるが、この中でも特にオレイン酸、ステアリン酸、牛
脂脂肪酸、硬化牛脂脂肪酸、パーム油脂脂肪酸、硬化パ
ーム油脂脂肪酸、パーム核油脂脂肪酸、硬化パーム核油
脂脂肪酸が好適である。なお、不飽和脂肪酸としては、
立体異性体がシス体またはトランス体であつても、ある
いは両者の混合物であつてもよいが、特にシス体/トラ
ンス体の比率が25/75〜100/0(重量比)であ
ることが好ましい。
The fatty acid residues --COR 8 , --COR 11 and --COR 12 in the above general formulas (I) and (II) are usually saturated higher fatty acids such as stearic acid and palmitic acid, oleic acid and elaidic acid, Derived from fatty acids obtained by decomposing and purifying unsaturated higher fatty acids such as linoleic acid and linolenic acid, natural fats and oils such as beef tallow, lard, palm oil, palm kernel oil, soybean oil, safflower oil, sunflower oil and olive oil. Among them, oleic acid, stearic acid, tallow fatty acid, hardened beef tallow fatty acid, palm fat and oil fatty acid, hardened palm fat and oil fatty acid, palm kernel fat and oil fatty acid, and hardened palm kernel fat and oil fatty acid are particularly preferable. In addition, as the unsaturated fatty acid,
The stereoisomer may be a cis isomer or a trans isomer, or a mixture of the two, and the ratio of the cis isomer / trans isomer is preferably 25/75 to 100/0 (weight ratio). .

【0016】上記一般式(I),(II)のジ長鎖アミン
は、通常用いられる酸で中和されて(a)成分のジ長鎖
アミン系柔軟基剤とされる。酸としては例えば、塩酸、
硫酸、リン酸などの無機塩や安息香酸、クエン酸、高分
子アクリル酸等の有機酸を挙げることができる。(a)
成分のアミン系柔軟基剤は、本発明の柔軟剤組成物中に
3〜30重量%配合するのが好適であり、好ましくは5
〜15重量%配合される。本発明の(b)成分として
は、下記化11の一般式(III) 又は(IV)で示される
モノ長鎖アミンの無機酸又は有機酸の中和物からなるモ
ノ長鎖アミン系柔軟基剤の1種または2種以上が用いら
れる。
The dilong-chain amines represented by the above general formulas (I) and (II) are neutralized with a commonly used acid to prepare the dilong-chain amine-based soft base of the component (a). Examples of the acid include hydrochloric acid,
Examples thereof include inorganic salts such as sulfuric acid and phosphoric acid, and organic acids such as benzoic acid, citric acid and polymeric acrylic acid. (A)
The amine softening agent as a component is preferably incorporated in the softening agent composition of the present invention in an amount of 3 to 30% by weight, preferably 5%.
˜15% by weight. As the component (b) of the present invention, a mono-long-chain amine-based soft base comprising a neutralized product of an inorganic acid or an organic acid of a mono-long-chain amine represented by the following general formula (III) or (IV) 1 type (s) or 2 or more types are used.

【0017】[0017]

【化11】 8 ,R11,R12は、炭素数8〜22の直鎖もしくは分
岐鎖アルキル基又はアルケニル基であり、好ましくは炭
素数13〜19の直鎖もしくは分岐鎖アルキル基又はア
ルケニル基である。n,mは、2〜10の整数であり、
好ましくは2〜4の整数である。pは、0又は1〜7の
整数であり、好ましくは0である。qは、1〜10の整
数であり、好ましくは1〜2の整数である。R10は、
H,OHあるいは炭素数1〜6のアルキル基又はヒドロ
キシアルキル基であり、好ましくはHである。
[Chemical 11] R 8, R 11, R 12 is a linear or branched alkyl or alkenyl group having 8 to 22 carbon atoms, preferably a straight-chain or branched alkyl or alkenyl group having 13 to 19 carbon atoms. n and m are integers of 2 to 10,
It is preferably an integer of 2 to 4. p is 0 or an integer of 1 to 7, preferably 0. q is an integer of 1 to 10, preferably an integer of 1 to 2. R 10 is
H, OH or an alkyl group having 1 to 6 carbon atoms or a hydroxyalkyl group, and preferably H.

【0018】(b)成分のモノ長鎖アミン系柔軟基剤の
一般式(III) 及び(IV)の具体例としては、以下の一
般式で示すものが挙げられる。
Specific examples of the general formulas (III) and (IV) of the mono-long-chain amine-based soft base material as the component (b) include those represented by the following general formula.

【0019】(1) 一般式(III) の具体例:化1
2,化13の(III−1)〜(III−6)
(1) Specific example of the general formula (III):
2, (III-1) to (III-6) of Chemical formula 13

【化12】 (上記一連の式中、nは2〜10の整数、qは1〜10
の整数を示す。)
[Chemical 12] (In the above series of formulas, n is an integer of 2 to 10 and q is 1 to 10
Indicates an integer. )

【0020】[0020]

【化13】 (上記一連の式中、nは2〜10の整数、qは1〜10
の整数を示す。)
[Chemical 13] (In the above series of formulas, n is an integer of 2 to 10 and q is 1 to 10
Indicates an integer. )

【0021】(2) 一般式(IV)の具体例:化14の
(IV−1)〜(IV−3)
(2) Specific examples of the general formula (IV): (IV-1) to (IV-3) of Chemical formula 14

【化14】 (上記一連の式中、mは2〜10の整数、qは1〜10
の整数を示す。)
[Chemical 14] (In the above series of formulas, m is an integer of 2 to 10, and q is 1 to 10
Indicates an integer. )

【0022】前記の一般式(III),(IV)中の脂肪酸残
基−COR8 ,−COR11,−COR12は通常、ステア
リン酸、パルミチン酸等の飽和高級脂肪酸、オレイン
酸、エライジン酸、リノール酸、リノレン酸等の不飽和
高級脂肪酸、牛脂、豚脂、パーム油、パーム核油、大豆
油、サフラワー油、ヒマワリ油、オリーブ油等の天然油
脂を分解、精製して得られる脂肪酸から由来するもので
あるが、この中でも特にオレイン酸、ステアリン酸、牛
脂脂肪酸、硬化牛脂脂肪酸、パーム油脂脂肪酸、硬化パ
ーム油脂脂肪酸、パーム核油脂脂肪酸、硬化パーム核油
脂脂肪酸が好適である。なお、不飽和脂肪酸としては、
立体異性体がシス体またはトランス体であつても、ある
いは両者の混合物であつてもよいが、特にシス体/トラ
ンス体の比率が25/75〜100/0(重量比)であ
ることが好ましい。
The fatty acid residues --COR 8 , --COR 11 and --COR 12 in the above general formulas (III) and (IV) are usually saturated higher fatty acids such as stearic acid and palmitic acid, oleic acid and elaidic acid, Derived from unsaturated fatty acids such as linoleic acid and linolenic acid, beef tallow, lard, palm oil, palm kernel oil, soybean oil, safflower oil, sunflower oil, olive oil and other natural fats and oils, which are obtained by decomposing and refining Among them, oleic acid, stearic acid, tallow fatty acid, hardened beef tallow fatty acid, palm fat and oil fatty acid, hardened palm fat and oil fatty acid, palm kernel fat and oil fatty acid, and hardened palm kernel fat and oil fatty acid are particularly preferable. In addition, as the unsaturated fatty acid,
The stereoisomer may be a cis isomer or a trans isomer, or a mixture of the two, and the ratio of the cis isomer / trans isomer is preferably 25/75 to 100/0 (weight ratio). .

【0023】上記一般式(III),(IV)のモノ長鎖アミ
ンは、通常用いられる酸で中和されて(b)成分のモノ
長鎖アミン系柔軟基剤とされる。酸としては例えば、塩
酸、硫酸、リン酸などの無機塩や安息香酸、クエン酸、
高分子アクリル酸等の有機酸を挙げることができる。
(b)成分は、本発明の柔軟剤組成物中に、0.1〜4
5重量%配合するのが好適であり、好ましくは0.5〜
15重量%配合される。(a)成分と(b)成分とは、
重量比で(a)/(b)=97/3〜40/60、好ま
しくは80/20〜50/50の範囲で柔軟剤組成物中
に配合される。この比率が97/3を越えると、残存ア
ニオン界面活性剤の影響を受けて柔軟性が低下してしま
う。一方60/40未満では、充分な柔軟性付与効果が
得られない。
The mono-long-chain amines represented by the above general formulas (III) and (IV) are neutralized with a commonly used acid to obtain the mono-long-chain amine-based soft base of the component (b). Examples of the acid include inorganic salts such as hydrochloric acid, sulfuric acid and phosphoric acid, benzoic acid, citric acid,
Organic acids such as polymeric acrylic acid can be mentioned.
The component (b) is contained in the softener composition of the present invention in an amount of 0.1 to 4
It is preferable to add 5% by weight, preferably 0.5 to
15 wt% is compounded. The component (a) and the component (b) are
The weight ratio of (a) / (b) = 97/3 to 40/60, preferably 80/20 to 50/50, in the softener composition. If this ratio exceeds 97/3, the flexibility decreases due to the influence of the residual anionic surfactant. On the other hand, if it is less than 60/40, a sufficient flexibility imparting effect cannot be obtained.

【0024】本発明の柔軟剤組成物には、上記成分以外
にその他の任意成分として、通常柔軟剤組成物に配合さ
れる公知の成分を本発明の効果を妨げない範囲で配合す
ることができる。任意成分としては、例えば、ジ長鎖ア
ルキルジ短鎖アルキル第4級アンモニウム塩等の第4級
アンモニウム塩、高級アルコールまたはモノアルキルア
ミンのアルキレンオキシド付加物等の非イオン界面活性
剤、食塩、塩化アンモニウム、塩化カルシウム、塩化マ
グネシウム、塩化カリウム等の水溶性塩、エチルアルコ
ール、イソプロピルアルコール、エチレングリコール、
プロピレングリコール、イソプレングリコール、ヘキシ
レングリコール等の溶剤、尿素、殺菌剤、酸化防止剤、
染料、顔料、シリコーン類、炭化水素、セルロース誘導
体、紫外線吸収剤、蛍光増白剤、香料等が挙げられる。
In addition to the above-mentioned components, the softener composition of the present invention may contain, as other optional components, known components which are usually incorporated in the softener composition, within a range that does not impair the effects of the present invention. . Examples of the optional component include quaternary ammonium salts such as dilong-chain alkyldishort-chain alkyl quaternary ammonium salts, nonionic surfactants such as higher alcohols or alkylene oxide adducts of monoalkylamines, sodium chloride, and ammonium chloride. , Water-soluble salts such as calcium chloride, magnesium chloride, potassium chloride, ethyl alcohol, isopropyl alcohol, ethylene glycol,
Solvents such as propylene glycol, isoprene glycol, hexylene glycol, urea, bactericides, antioxidants,
Examples thereof include dyes, pigments, silicones, hydrocarbons, cellulose derivatives, ultraviolet absorbers, optical brighteners and fragrances.

【0025】[0025]

【発明の効果】本発明によれば、(a)成分のジ長鎖ア
ミン系柔軟基剤と、(b)成分のモノ長鎖アミン系柔軟
基剤とを特定比率で併用して柔軟剤組成物とすることに
より、洗濯サイクルから持ち込まれるアニオン界面活性
剤の存在下でも衣料に対して柔軟性を付与することがで
き、特に全自動洗濯機での使用に好適である。
According to the present invention, the softening agent composition is prepared by using the dilong-chain amine-based softening agent as the component (a) and the mono-long-chaining amine-based softening agent as the component (b) in a specific ratio. By making it a product, it is possible to impart flexibility to clothing even in the presence of an anionic surfactant brought in from the washing cycle, and it is particularly suitable for use in a fully automatic washing machine.

【0026】[0026]

【実施例】以下、実施例により本発明をさらに詳細に説
明するが、それに先立つて実施例で採用した評価方法を
説明する。
EXAMPLES The present invention will be described in more detail with reference to examples below, but prior to that, the evaluation methods adopted in the examples will be described.

【0027】(1) 柔軟化処理方法 木綿として市販の綿タオルを、また、化学繊維としてア
クリルジャージを用い、市販衣料用洗剤「ハイトツプ」
(ライオン(株)製)により電気洗濯機を用いて50℃
で2回繰り返し洗濯後、常温の水道水で1回すすぎ、こ
れを試験布とした。次に、25℃の水道水30リツトル
に対し、(a)成分と(b)成分の合計量として1gに
なるように柔軟剤組成物を加えて均一溶液とした。この
溶液中に浴比30倍で綿タオルとアクリルジャージの比
率を7/3として各試験布を浸し3分間処理した後、2
分間脱水した。このように処理した布を風乾した後、2
5℃、65%RHの条件で24時間放置し、評価試験に
用いた。
(1) Softening treatment method A commercially available cotton towel, and an acrylic jersey as a chemical fiber are used, and a commercial clothing detergent "HITOPUP" is used.
(Lion Co., Ltd.) using an electric washing machine at 50 ℃
After being repeatedly washed twice, the test cloth was rinsed once with room temperature tap water. Next, the softener composition was added to 30 liters of tap water at 25 ° C. so that the total amount of the components (a) and (b) would be 1 g to prepare a uniform solution. Each test cloth was dipped in this solution with a bath ratio of 30 times and the ratio of cotton towel and acrylic jersey was 7/3, and treated for 3 minutes, and then 2
Dehydrated for a minute. After air-drying the thus treated cloth, 2
It was left for 24 hours under the conditions of 5 ° C. and 65% RH and used for the evaluation test.

【0028】(2) 柔軟性評価方法 ジメチルジステアリル第4級アンモニウムクロライドを
柔軟剤基剤として配合した柔軟剤組成物で処理した布を
対照にして一対比較を行い、下記基準にて5名が評価
し、平均値を評価結果とした。 +2:対照より柔らかい +1:対照よりやや柔らかい 0:対照と同じ −1:対照の方がやや柔らかい −2:対照の方が柔らかい
(2) Softness evaluation method A pair of comparisons were carried out with a cloth treated with a softening agent composition containing dimethyl distearyl quaternary ammonium chloride as a softening agent base, and a pair of comparisons were conducted. It evaluated and made the average value the evaluation result. +2: Softer than control +1: Slightly softer than control 0: Same as control -1: Slightly softer control -2: Softer control

【0029】実施例1〜7、比較例1〜5 以下に表1に示した(a)成分と(b)成分とを用い、
表2に示した柔軟基剤を含有する柔軟剤組成物を調製し
て柔軟性を評価し、その結果を表2に示した。
Examples 1 to 7 and Comparative Examples 1 to 5 Using the components (a) and (b) shown in Table 1 below,
The softening agent composition containing the softening agent shown in Table 2 was prepared and the softness was evaluated, and the results are shown in Table 2.

【0030】[0030]

【表1】表1:(a)成分及び(b)成分 記号 化合物名 a成分: a−1 (I−1)式でn=3、q=1の塩酸中和物(ジエステルジアミン) a−2 (I−2)式でn=3、q=1の塩酸中和物(ジエステルジアミン) a−3 (I−6)式でn=3、q=1の塩酸中和物(ジエステルジアミン) a−4 (I−7)式でn=3の塩酸中和物(ジアミドジアミン) a−5 (II−1)式でm=3、q=1の塩酸中和物(アミドエステルアミン) a−6 (II−6)式でm=3の塩酸中和物(ジアミドアミン) a−7 (I−1)式でn=15、q=15の塩酸中和物(比較品) a−8 ジメチルジステアリル第4級アンモニウムクロライド(対照) b成分: b−1 (III−1)式ではn=3、q=1の塩酸中和物 b−2 (III−4)式ではn=3、q=1の塩酸中和物 b−3 (III−5)式ではn=3、q=1の塩酸中和物 b−4 (IV−1)式ではm=3、q=1の塩酸中和物 b−5 (III−1)式ではn=15、q=15の塩酸中和物(比較品) [Table 1]Table 1: (a) component and (b) component symbol Compound name Component a: a-1 (I-1) n = 3, q = 1 hydrochloric acid neutralized product (diesterdiamine) a-2 (I-2) n = 3, q = 1 hydrochloric acid neutralized (Diester diamine) a-3 (I-6) formula, n = 3, q = 1 neutralized hydrochloric acid (diester diamine) a-4 (I-7) formula, n = 3 hydrochloric acid neutralized product ( Diamidediamine) a-5 (II-1) formula, m = 3, q = 1 hydrochloric acid neutralized product (amidoesteramine) a-6 (II-6) formula, m = 3 hydrochloric acid neutralized product (diamine Amidoamine) a-7 (I-1) formula, n = 15, q = 15 hydrochloric acid neutralized product (comparative product) a-8 dimethyl distearyl quaternary ammonium chloride (control) Component b: b-1 (III-1) formula: n = 3, q = 1 hydrochloric acid neutralized product b-2 (III-4) formula: n = 3, q = 1 hydrochloric acid neutralized product b-3 Hydrochloric acid neutralized product of n = 3 and q = 1 in the formula (III-5) b-4 Neutralized hydrochloric acid of m = 3 and q = 1 in the formula (IV-1) In the formula b-5 (III-1), hydrochloric acid neutralized product of n = 15 and q = 15 (comparative product)

【0031】[0031]

【表2】表2:基剤組成及び評価結果 (a)成分 (b)成分 (a)/(b) 評価結果:柔軟性 化合物 化合物 重量比 木綿 アクリル 実施例1 a−1 b−1 60/40 +1.4 +2.0 比較例1 a−1 − 100/0 0 +0.8 比較例2 − b−1 0/100 −2.0 −2.0 比較例3 a−1 b−1 20/80 −1.2 +1.0 比較例4 a−7 b−1 60/40 −0.8 +1.0 比較例5 a−1 b−5 60/40 −1.2 0 実施例2 a−1 b−3 95/5 +1.0 +1.4 実施例3 a−2 b−4 50/50 +1.6 +2.0 実施例4 a−3 b−2 60/40 +1.4 +1.8 実施例5 a−4 b−1 40/60 +0.8 +2.0 実施例6 a−5 b−3 70/30 +2.0 +1.2 実施例7 a−6 b−3 60/40 +1.4 +1.2 対照 a−8 − − 基準 基準 Table 2: Base composition and evaluation results Component (a) Component (b) Component (a) / (b) Evaluation result: Flexible compound Compound weight ratio Cotton acrylic Example 1 a-1 b-1 60 / 40 +1.4 +2.0 Comparative Example 1 a-1 −100/0 0 +0.8 Comparative Example 2 −b−1 0/100 −2.0 −2.0 Comparative Example 3 a−1 b−1 20/80 −1.2 +1 .0 Comparative Example 4 a-7 b-1 60/40 -0.8 +1.0 Comparative Example 5 a-1 b-5 60/40 -1.2 0 Example 2 a-1 b-3 95/5 +1.0 +1 .4 Example 3 a-2 b-4 50/50 +1.6 +2.0 Example 4 a-3 b-2 60/40 +1.4 +1.8 Example 5 a-4 b-1 40/60 +0.8 +2.0 Example 6 a-5 b-3 70/30 +2.0 +1.2 Example 7 a-6 b-3 60/40 +1.4 +1.2 Control a-8 − − Standard Reference

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 D06M 13/372 13/419 D06M 13/40 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification number Office reference number FI technical display location D06M 13/372 13/419 D06M 13/40

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 (a) 下記化1の一般式(I)及び/
又は(II)で示されるアミンの無機酸又は有機酸の中和
物からなるジ長鎖アミン系柔軟基剤 【化1】 (b) 下記化2の一般式(III) 及び/又は(IV)で
示されるアミンの無機酸又は有機酸の中和物からなるモ
ノ長鎖アミン系柔軟基剤 【化2】 を(a)及び(b)成分の配合重量比が(a)/(b)
=97/3〜40/60の範囲で含有することを特徴と
する柔軟剤組成物。
1. (a) General formula (I) and //
Or a di-long-chain amine-based soft base consisting of a neutralized amine or organic acid of amine represented by (II) (B) A mono-long-chain amine-based soft base consisting of a neutralized product of an inorganic acid or an organic acid of an amine represented by the following general formula (III) and / or (IV) The blending weight ratio of the components (a) and (b) is (a) / (b)
= 97/3 to 40/60 in the range of the softening agent composition.
JP18705093A 1993-06-29 1993-06-29 Softening agent composition Pending JPH0718571A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Application Number Priority Date Filing Date Title
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Publication Number Publication Date
JPH0718571A true JPH0718571A (en) 1995-01-20

Family

ID=16199302

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Country Status (1)

Country Link
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US5670472A (en) * 1994-04-19 1997-09-23 Witco Corporation Biodegradable ester diquaternary compounds and compositions containing them
EP0803498A1 (en) * 1996-04-26 1997-10-29 Witco Corporation Polyester, polyquaternary compounds, compositions containing them and their use as fabric softener
WO2000021918A1 (en) * 1998-10-13 2000-04-20 Goldschmidt Chemical Corporation Polyester polyquaternary compounds, compositions containing them, and uses thereof
US6211139B1 (en) 1996-04-26 2001-04-03 Goldschmidt Chemical Corporation Polyester polyquaternary compounds, compositions containing them, and use thereof
US6596685B2 (en) 2000-01-19 2003-07-22 Kao Corporation Softener composition
WO2006040332A1 (en) * 2004-10-13 2006-04-20 Clariant Finance (Bvi) Limited Fatty acid esters of alkanolamines and their use as softening agents
WO2007094388A1 (en) * 2006-02-15 2007-08-23 Nof Corporation Softening agent for paper and method for making paper by using same
JP2007217816A (en) * 2006-02-15 2007-08-30 Nof Corp Paper softener and method for producing paper using the same
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Publication number Priority date Publication date Assignee Title
US5670472A (en) * 1994-04-19 1997-09-23 Witco Corporation Biodegradable ester diquaternary compounds and compositions containing them
EP0803498A1 (en) * 1996-04-26 1997-10-29 Witco Corporation Polyester, polyquaternary compounds, compositions containing them and their use as fabric softener
US6211139B1 (en) 1996-04-26 2001-04-03 Goldschmidt Chemical Corporation Polyester polyquaternary compounds, compositions containing them, and use thereof
WO2000021918A1 (en) * 1998-10-13 2000-04-20 Goldschmidt Chemical Corporation Polyester polyquaternary compounds, compositions containing them, and uses thereof
US6596685B2 (en) 2000-01-19 2003-07-22 Kao Corporation Softener composition
US7202203B2 (en) 2000-01-19 2007-04-10 Kao Corporation Softener composition
WO2006040332A1 (en) * 2004-10-13 2006-04-20 Clariant Finance (Bvi) Limited Fatty acid esters of alkanolamines and their use as softening agents
JP2007217816A (en) * 2006-02-15 2007-08-30 Nof Corp Paper softener and method for producing paper using the same
WO2007094388A1 (en) * 2006-02-15 2007-08-23 Nof Corporation Softening agent for paper and method for making paper by using same
US7947151B2 (en) 2006-02-15 2011-05-24 Nof Corporation Softening agent for paper and method for making paper by using same
JP2007224444A (en) * 2006-02-22 2007-09-06 Nof Corp Paper softener and method for producing paper using the same
US8261785B2 (en) 2008-06-24 2012-09-11 Toyo Jidoki Co., Ltd Gripper for an automatic bag filling apparatus
WO2010108108A3 (en) * 2009-03-20 2011-04-07 Egen, Inc. Polyamine derivatives
US8900621B2 (en) 2009-03-20 2014-12-02 Clsn Laboratories, Inc. Polyamine derivatives
US8932638B2 (en) 2009-03-20 2015-01-13 Clsn Laboratories, Inc. Polyamine derivatives
JP2015147927A (en) * 2009-03-20 2015-08-20 エーゲン、インコーポレイテッド Polyamine derivatives
US9254334B2 (en) 2009-03-20 2016-02-09 Clsn Laboratories, Inc. Polyamine derivatives

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