JPH0441774A - Liquid soft finishing agent - Google Patents

Liquid soft finishing agent

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Publication number
JPH0441774A
JPH0441774A JP14350690A JP14350690A JPH0441774A JP H0441774 A JPH0441774 A JP H0441774A JP 14350690 A JP14350690 A JP 14350690A JP 14350690 A JP14350690 A JP 14350690A JP H0441774 A JPH0441774 A JP H0441774A
Authority
JP
Japan
Prior art keywords
compound
finishing agent
formula
hydrocarbon group
dispersibility
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
JP14350690A
Other languages
Japanese (ja)
Inventor
Masaaki Yamamura
正明 山村
Junichi Inokoshi
猪腰 淳一
Kazutaka Shirato
和隆 白土
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.)
Kao Corp
Original Assignee
Kao 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 Kao Corp filed Critical Kao Corp
Priority to JP14350690A priority Critical patent/JPH0441774A/en
Publication of JPH0441774A publication Critical patent/JPH0441774A/en
Pending legal-status Critical Current

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  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

PURPOSE:To obtain a liquid soft finishing agent for domestic use giving excellent softness to various fibers and exhibiting excellent dispersibility in rinsing water containing a quaternary an amide compound obtained by condensation reaction of a specific diamine and fatty acid, as an essential ingredient. CONSTITUTION:Diamine expressed by formula I (R<1> is 8-24C hydrocarbon group; (n) is 2 or 3) is subjected to condensation reaction with a compound expressed by formula II (R<2> is 7-23C hydrocarbon group) to obtain an amine having amide bonding. Next, said amine is made to quaternary compound by methyl chloride, etc., and the resultant compound is mixed with inorganic electrolyte (e.g. sodium chloride) in an amount of 0.3-20wt.% of the above-mentioned amine compound to afford a liquid soft finishing agent having extremely excellent dispersibility. Said finishing agent has excellent dispersibility in rinsing water in domestic washing and also imparts excellent softness and softness with enriched elasticity to various fibers.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、液体柔軟仕上剤に関し、詳しくは各種の繊維
に対して、優れた柔軟性を付与し、かつすすぎ水中への
分散性の良い家庭用液体柔軟仕上剤に関するものである
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a liquid fabric softener that imparts excellent flexibility to various fibers and has good dispersibility in rinsing water. This invention relates to household liquid fabric softeners.

〔従来の技術及び発明が解決しようとする課題〕現在、
家庭用柔軟仕上剤として市販されている商品は殆どがジ
(硬化牛脂アルキル)ジメチルアンモニウムクロライド
に代表されるような1分子中に2個の長鎖アルキル基を
有する第4級アンモニウム塩を主成分とした組成物であ
る。
[Problems to be solved by conventional techniques and inventions] Currently,
Most commercially available household fabric softeners contain quaternary ammonium salts with two long-chain alkyl groups in each molecule, such as di(hardened tallow alkyl)dimethylammonium chloride. It is a composition with

この理由としては第4級アンモニウム塩は少量で各種繊
維に対して良好な柔軟効果を有するからである。
The reason for this is that a small amount of quaternary ammonium salt has a good softening effect on various fibers.

上記の第4級アンモニウム塩を主基割とする柔軟仕上剤
は通常4〜20%の分散液として市販され、使用されて
いる。
The above-mentioned fabric softeners mainly composed of quaternary ammonium salts are commercially available and used as dispersions of 4 to 20%.

第4級アンモニウム塩は疎水性が強いためすすぎ水中に
投入する際、攪拌力が弱い場合は水への分散性が悪く、
そのため衣料に対してムラ付きするおそれがある。市販
の柔軟剤は上記の第4級アンモニウム塩の他に様々な添
加剤を配合し、水への分散性を改良しているが、その効
果は未だ不充分である。
Quaternary ammonium salts are highly hydrophobic, so if the stirring force is weak when adding them to the rinsing water, they will have poor dispersibility in water.
Therefore, there is a possibility that it may become uneven on clothing. Commercially available softeners contain various additives in addition to the above-mentioned quaternary ammonium salt to improve their dispersibility in water, but their effects are still insufficient.

多くの第4級アンモニウム塩を柔軟基剤とする液体柔軟
仕上剤が検討されている0例えば、特開平2−6664
号公報には窒素数が3以上のN−アルキルアミンと高級
脂肪酸の縮合物である部分アミド化物の4級化物を含有
する柔軟仕上剤が、特開昭55−76168号公報には
N、 N’−ジアルキルアルキレンジアミンの4級化物
を含有する柔軟剤が記載されているが、これらの水への
分散性は未だ不充分である。
Liquid softeners using many quaternary ammonium salts as softening bases have been studied. For example, JP-A-2-6664
JP-A-55-76168 discloses a softening agent containing a quaternized partially amidated product which is a condensation product of an N-alkylamine having 3 or more nitrogen atoms and a higher fatty acid; Softeners containing quaternized products of '-dialkylalkylene diamines have been described, but their dispersibility in water is still insufficient.

〔課題を解決するための手段〕[Means to solve the problem]

本発明者らは上記の実情に鑑み、優れた柔軟性を有し、
且つ水への分散性の良好な柔軟仕上剤を提供すべく鋭意
研究した結果、特殊なアミドアミン化合物の4級化物が
柔軟性に優れ、しかもすすぎ水中への分散性が非常に良
好なことを見出し本発明を完成するに至った。
In view of the above circumstances, the present inventors have excellent flexibility,
As a result of intensive research to provide a fabric softener with good dispersibility in water, we discovered that a quaternized product of a special amidoamine compound has excellent flexibility and has very good dispersibility in rinsing water. The present invention has now been completed.

すなわち本発明は、下記の(a)成分を必須成分として
含有することを特徴とする液体柔軟仕上剤を提供するも
のである。
That is, the present invention provides a liquid fabric softener characterized by containing the following component (a) as an essential component.

(a)  一般式(I)で示されるジアミンと一般式(
II)で示される脂肪酸との縮合反応により得られるア
ミドアミン化合物の4級化物。
(a) Diamine represented by general formula (I) and general formula (
A quaternized product of an amidoamine compound obtained by a condensation reaction with a fatty acid represented by II).

R’NHC−Hz−NHz         (I )
j R”−C−OH (II) 〔式中、R1は炭素数8〜24の直鎖又は分岐鎖の飽和
又は不飽和の炭化水素基、R1は炭素数7〜23の直鎖
又は分岐鎖の飽和又は不飽和の炭化水素基、閣は2又は
3、好ましくは3である。〕 本発明で使用するアミドアミン化合物の4級化物はN)
式で示されるジアミン1モルと(II)式で示される脂
肪酸1〜2モルの縮合反応によって得られるアミド結合
を有するアミンを常法によりメチルクロライド、ジメチ
ル硫酸、ジエチル硫酸等で4級化することにより得られ
る。
R'NHC-Hz-NHz (I)
j R''-C-OH (II) [In the formula, R1 is a straight chain or branched saturated or unsaturated hydrocarbon group having 8 to 24 carbon atoms, and R1 is a straight chain or branched chain having 7 to 23 carbon atoms. The saturated or unsaturated hydrocarbon group is 2 or 3, preferably 3.] The quaternized product of the amidoamine compound used in the present invention is N)
Quaternizing an amine having an amide bond obtained by a condensation reaction of 1 mole of the diamine represented by the formula and 1 to 2 moles of the fatty acid represented by the formula (II) with methyl chloride, dimethyl sulfate, diethyl sulfate, etc. by a conventional method. It is obtained by

この反応に用いられる脂肪酸としては、ヤシ油、パーム
油、牛脂、ナタネ油、魚油等の天然油脂由来のものが一
般的であるが、化学的に合成した脂肪酸でも良い。
The fatty acids used in this reaction are generally derived from natural oils such as coconut oil, palm oil, beef tallow, rapeseed oil, and fish oil, but chemically synthesized fatty acids may also be used.

一般式(1)及び(I[)において、R1,R1の少な
くとも1方は炭素数16以上であることが望ましい。
In general formulas (1) and (I[), at least one of R1 and R1 preferably has 16 or more carbon atoms.

本発明において、(→成分は組成物中に1〜30重量%
、好ましくは4〜30重量%、特に好ましくは10〜2
5重量%配合される。
In the present invention, (→ component is 1 to 30% by weight in the composition)
, preferably 4 to 30% by weight, particularly preferably 10 to 2% by weight
It is blended in an amount of 5% by weight.

本発明の組成物は、例えばアミドアミン化合物の4級化
物の溶融物又は濃厚物を攪拌又は剪断混合下に水溶液中
にゆっくり添加することにより得られるが、この方法に
限定されるものではなく、中和物を予め製造する或いは
中和剤を後添加する等の方法によって得ることもできる
The composition of the present invention can be obtained, for example, by slowly adding a melt or concentrate of a quaternized amidoamine compound to an aqueous solution under stirring or shear mixing, but the method is not limited to this method. It can also be obtained by a method such as preparing a hydrate in advance or adding a neutralizing agent afterward.

組成物調製時には減粘及び分散性を更によくするために
無機電解質を(a)成分に対して0.3〜20重量%、
好ましくは0.6〜10重量%、特に好ましくは0.6
〜5重量%添加することが望ましい。無I!電解質とし
ては塩化ナトリウム、臭化ナトリウム、塩化カルシウム
、塩化マグネシウム等が挙げられる。
When preparing the composition, in order to further improve viscosity reduction and dispersibility, 0.3 to 20% by weight of an inorganic electrolyte is added to component (a).
Preferably 0.6 to 10% by weight, particularly preferably 0.6
It is desirable to add up to 5% by weight. No I! Examples of the electrolyte include sodium chloride, sodium bromide, calcium chloride, and magnesium chloride.

また、水への分散性及び好ましい柔軟効果を発現させる
ためには、(a)成分の平均粒子径を0.1〜5−の範
囲にすることが望ましい、平均粒子径をこの範囲に調整
するための最も適切な方法は(a)成分の種類と量に応
じて配合時の攪拌剪断力を調整することである。平均粒
子径が0.1虜未満の場合は柔軟性が低下する傾向があ
り、5虜より大きいと水への分散性が低下する傾向があ
る。
In addition, in order to exhibit dispersibility in water and a preferable softening effect, it is desirable that the average particle size of component (a) be in the range of 0.1 to 5-5, and the average particle size should be adjusted within this range. The most appropriate method for this is to adjust the stirring shear force during blending depending on the type and amount of component (a). If the average particle diameter is less than 0.1 mm, the flexibility tends to decrease, and if it is larger than 5 mm, the dispersibility in water tends to decrease.

本発明の液体柔軟仕上剤には従来一般に使用されている
、例えば以下に示すような第4級アンモニウム塩を配合
することができる。
The liquid softener of the present invention may contain quaternary ammonium salts that have been commonly used, such as those shown below.

〔式中、H2,H4,R@及びR9はそれぞれ炭素数1
0〜24のアルキル基、アルケニル基又はβ−ヒドロキ
シアルキル基であり、R5,R6及びR7はそれぞれ炭
素数1〜3のアルキル基もしくはヒドロキシアルキル基
、ベンジル基又は−(ctn4o) q−n (但し、
qは1〜3である)を示し、Xはハロゲン又は炭素数1
〜3のアルキル基を有するモノアルキル硫酸塩基を示す
、〕一般式(III)で表される化合物の例としては例
えばシタロージメチルアンモニウムクロライド、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ライド、ジステ
アリルジメチルアンモニウムクロライド、ジベヘニルジ
メチルアンモニウムクロライド、ジオレイルジメチルア
ンモニウムクロライド等が挙げられる。
[In the formula, H2, H4, R@ and R9 each have 1 carbon number
0 to 24 alkyl group, alkenyl group, or β-hydroxyalkyl group, and R5, R6, and R7 are each an alkyl group or hydroxyalkyl group having 1 to 3 carbon atoms, a benzyl group, or -(ctn4o)qn (however, ,
q is 1 to 3), and X is halogen or carbon number 1
Examples of the compound represented by the general formula (III), which represents a monoalkyl sulfate group having ~3 alkyl groups, include citalodimethylammonium chloride, citalodimethylammonium methyl sulfate, and di(hydrogenated tallow) dimethyl. Examples include ammonium chloride, distearyldimethylammonium chloride, dibehenyldimethylammonium chloride, dioleyldimethylammonium chloride, and the like.

一般式(TV)で表される化合物の例としては例えばモ
ノクロ−トリメチルアンモニウムクロライド、モノ (
水素添加タロー)トリメチルアンモニウムクロライド等
が挙げられる。
Examples of compounds represented by the general formula (TV) include monochrome-trimethylammonium chloride, mono(
Examples include hydrogenated tallow) trimethylammonium chloride.

一般式(V、)で表される化合物の例としては例えば1
−メチル−1−タローアミド−エチル−2−タローイミ
ダゾリニウムメチルサルフェート、l−メチル−1−(
水素添加タロータローアミドエチル)イミダゾリニウム
メチルサルフェート等が挙げられる。
Examples of compounds represented by the general formula (V,) include 1
-Methyl-1-tallowamido-ethyl-2-tallowimidazolinium methyl sulfate, l-methyl-1-(
Examples include hydrogenated tallow tallow amidoethyl) imidazolinium methyl sulfate.

一般式(Vl)で表される化合物の例としては例えばメ
チルビス(タローイルオキシエチル)(2−ヒドロキシ
エチル)アンモニウムクロライド、メチルビス(ステア
ロイルオキシエチル)(2−ヒドロキシエチル)アンモ
ニウムメチルサルフェート等が挙げられる。
Examples of the compound represented by the general formula (Vl) include methylbis(tallowyloxyethyl)(2-hydroxyethyl)ammonium chloride, methylbis(stearoyloxyethyl)(2-hydroxyethyl)ammonium methylsulfate, etc. .

一般式(■)で表される化合物の例としては例えばメチ
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及びメチルビス(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等が挙げられる。
Examples of compounds represented by the general formula (■) include methylbis(tallowamideethyl)(2-hydroxyethyl)ammonium methylsulfate and methylbis(hydrogenated tallowamideethyl)(2-hydroxyethyl)
Examples include ammonium methyl sulfate.

これらの第4級アンモニウム塩を併用することにより衣
料に弾力性(ふっくら感)のある柔らかさも付与するこ
とができる。
By using these quaternary ammonium salts in combination, it is possible to impart softness with elasticity (fluffiness) to clothing.

更に、本発明の液体柔軟仕上剤には保存安定性の改善の
ためにポリオキシエチレン(5〜50モル)アルキル又
はアルケニル(Cz*〜84)エーテル等のノニオン界
面活性剤、エタノール、プロピレングリコールやエチレ
ングリコールのような溶剤又は尿素、吸水性改善のため
にポリジメチルシロキサン、ポリエーテル変性シリコー
ン、アミノ変性シリコーン等のシリコーン類、製品の外
観のために顔料又は染料を、仕上がりの白さのために螢
光増白剤を、そして使用時及び仕上がり後の趣向を良く
するために香料等を配合することもできる。
Furthermore, the liquid fabric softener of the present invention may contain nonionic surfactants such as polyoxyethylene (5 to 50 mol) alkyl or alkenyl (Cz* to 84) ether, ethanol, propylene glycol, etc. to improve storage stability. Solvents such as ethylene glycol or urea; silicones such as polydimethylsiloxane, polyether-modified silicone, and amino-modified silicone to improve water absorption; pigments or dyes to improve the appearance of the product; and pigments or dyes to improve the whiteness of the finish. A fluorescent brightener and a fragrance can also be added to improve the appearance during use and after finishing.

〔実 施 例〕〔Example〕

次に本発明を実施例をもって詳述するが、本発明はこれ
らの実施例に限定されるものではない。
Next, the present invention will be explained in detail with reference to Examples, but the present invention is not limited to these Examples.

本発明に使用されるアミドアミン化合物の4級化物の製
造方法を合成例によって示す。
A method for producing a quaternized amidoamine compound used in the present invention will be illustrated by a synthesis example.

合成例 ステアリン酸568 g (2モル)にN−ラウリルプ
ロピレンジアミン484 g (2モル)ヲ加工、17
0〜190°Cで3時間反応させ、35gの水を溜出さ
せ、アミドアミン化合物を得た。
Synthesis Example 568 g (2 mol) of stearic acid was processed with 484 g (2 mol) of N-laurylpropylene diamine, 17
The reaction was carried out at 0 to 190°C for 3 hours, and 35 g of water was distilled off to obtain an amidoamine compound.

このアミドアミン化合物を既知の方法により4級化し、
本発明の化合物(a−1)を得た。
This amidoamine compound is quaternized by a known method,
Compound (a-1) of the present invention was obtained.

同様にして表1に示す様な本発明の化合物(a−2)〜
(a−5)を合成した。
Similarly, compounds (a-2) of the present invention as shown in Table 1
(a-5) was synthesized.

表   1(a)成分の組成 実施例1〜13及び比較例1 表2に示す配合の組成物について、以下の方法により柔
軟性、水分散性の評価を行った。
Composition of Table 1 (a) Component Examples 1 to 13 and Comparative Example 1 The compositions having the formulations shown in Table 2 were evaluated for flexibility and water dispersibility by the following methods.

〈柔軟性の評価〉 (1)処理方法 市販の木綿タオル2kg、アクリルシャーシー1kgを
3.5” DH硬水にて市販洗剤アタック(花王株式会
社製、登録商標)にて5回繰り返し洗濯(301洗濯機
)をし、各繊維についていた繊維処理剤を除去した後、
表2の配合組成物の15%分散液10ccにて25°C
,1分間撹拌下で処理した。
<Evaluation of flexibility> (1) Processing method 2 kg of commercially available cotton towels and 1 kg of acrylic chassis were washed 5 times with commercially available detergent Attack (manufactured by Kao Corporation, registered trademark) in 3.5” DH hard water (301 After washing the fabric (washing machine) and removing the fiber treatment agent attached to each fiber,
25°C at 10cc of a 15% dispersion of the blended composition in Table 2.
, under stirring for 1 minute.

(2)評価方法 上記方法で処理した布を室内で風乾後、25℃、65%
RHの恒温恒湿室にて24時間放置した。
(2) Evaluation method After drying the cloth treated with the above method indoors, 25℃, 65%
It was left in a constant temperature and humidity room at RH for 24 hours.

これらの布について柔軟性の評価を行った。The flexibility of these fabrics was evaluated.

柔軟性の評価は、ジ水素添加牛脂アルキルジメチルアン
モニウムクロライド15重量%からなる柔軟剤10cc
で処理した布を対照にして一対比較を行った。評価は次
のように表す。
The softness evaluation was performed using 10cc of a softener made of 15% by weight of dihydrogenated beef tallow alkyldimethylammonium chloride.
Pairwise comparisons were made using the treated fabric as a control. The evaluation is expressed as follows.

+2・対照より柔らかい +l;対照よりやや柔らかい 0 対照と同じ −1・対照がやや柔らかい −2・対照が柔らかい 〈水分散性の評価〉 日立製全自動洗濯II(製品名[静御前forBio 
65J )に高水位まで水を入れソフト水流で2分間運
転をする。運転を止めた後、5秒後に表2の組成物を投
入し、5.10.30秒後の分散性を観察した。評価は
次のように表す。
+2・Softer than the control +l; Slightly softer than the control 0 Same as the control −1・Slightly softer than the control −2・Softer than the control <Evaluation of water dispersibility> Hitachi fully automatic washing II (product name [Shizuka Gozen for Bio
Fill a 65J) with water to a high water level and run it for 2 minutes with a soft water flow. After stopping the operation, the composition shown in Table 2 was added 5 seconds later, and the dispersibility was observed 5.10.30 seconds later. The evaluation is expressed as follows.

+2;5秒後に均一に分散 +1;10秒後に均一に分散 0;30秒後に均一に分散 −1;30秒後では一部不均一 一2i30秒後でも全く分、散しない 表2に示すように、本発明の化合物を使用することによ
り、柔軟性と水への分散性の両者を満足する効果が得ら
れる。
+2; Uniformly dispersed after 5 seconds +1; Uniformly dispersed after 10 seconds 0; Uniformly dispersed after 30 seconds -1; Partially uneven after 30 seconds - 2i Not dispersed or dispersed at all even after 30 seconds Shown in Table 2 Thus, by using the compound of the present invention, an effect that satisfies both flexibility and water dispersibility can be obtained.

表 2 柔軟性、水分散性 注) 率1電解質の配合量;(a)成分に対する重量%本2粒
子径;光散乱法測定器により測定率3a−6;ジ硬化牛
脂アルキルジメチルアンモニウムクロライド 尚、(a)成分の組成物中の配合量は15重量%である
Table 2 Flexibility, water dispersibility (Note) Rate 1 Blend amount of electrolyte; Weight % with respect to component (a) 2 Particle diameter; Rate 3a-6 measured by light scattering measuring instrument; Dihardened beef tallow alkyl dimethyl ammonium chloride; The amount of component (a) in the composition is 15% by weight.

実施例14 下記組成物を調製し、実施例1〜13と同様にして柔軟
性及び水分散性を評価した。その結果、柔軟性は+1、
水分散性は+2であった。
Example 14 The following compositions were prepared and evaluated for flexibility and water dispersibility in the same manner as Examples 1-13. As a result, flexibility is +1,
Water dispersibility was +2.

L金皿爪 a −112重量% 弾力性の評価を行なった。L gold plate claw a -112% by weight Elasticity was evaluated.

〈弾力性の評価〉 実施例1〜13と同様に処理した木綿タオルを8つ折り
にして3枚重ねて積み上げ、5g/dの圧力で5分間加
圧した後、圧力を取り除き、タオルの高さを測定した。
<Evaluation of elasticity> Cotton towels treated in the same manner as in Examples 1 to 13 were folded into 8 and stacked in 3 layers, and after pressurizing at a pressure of 5 g/d for 5 minutes, the pressure was removed and the height of the towel was adjusted. was measured.

タオルの高さが高い程、弾力性は良好である。The higher the height of the towel, the better the elasticity.

その結果、上記組成物で処理した時のタオルの高さは9
.8C11、比較例1の組成物で処理した時のタオルの
高さは8.8CIlであった。
As a result, the height of the towel when treated with the above composition was 9
.. 8C11, the height of the towel when treated with the composition of Comparative Example 1 was 8.8 CIl.

CaC1t                  O,
15香料     0.3 水             バランス尚、分散粒子の
平均粒子径は1.3μである。
CaC1tO,
15 Perfume 0.3 Water Balance Note that the average particle diameter of the dispersed particles is 1.3μ.

Claims (1)

【特許請求の範囲】 1 下記の(a)成分を必須成分として含有することを
特徴とする液体柔軟仕上剤。 (a)一般式( I )で示されるジアミンと一般式(II
)で示される脂肪酸との縮合反応により得られるアミド
アミン化合物の4級化物。 R^1NHC_mH_2_mNH_2( I )▲数式、
化学式、表等があります▼(II) 〔式中、R^1は炭素数8〜24の直鎖又は分岐鎖の飽
和又は不飽和の炭化水素基、R^2は炭素数7〜23の
直鎖又は分岐鎖の飽和又は不飽和の炭化水素基、mは2
又は3である。〕 2 更に無機電解質を(a)成分に対して0.3〜20
重量%含有してなる請求項1記載の液体柔軟仕上剤。
[Scope of Claims] 1. A liquid fabric softener characterized by containing the following component (a) as an essential component. (a) Diamine represented by general formula (I) and general formula (II)
) A quaternized product of an amidoamine compound obtained by a condensation reaction with a fatty acid represented by R^1NHC_mH_2_mNH_2(I)▲Formula,
Chemical formulas, tables, etc. are available▼(II) [In the formula, R^1 is a straight chain or branched saturated or unsaturated hydrocarbon group having 8 to 24 carbon atoms, and R^2 is a straight chain having 7 to 23 carbon atoms. chain or branched saturated or unsaturated hydrocarbon group, m is 2
Or 3. ] 2 Furthermore, the amount of inorganic electrolyte is 0.3 to 20% relative to component (a).
% by weight of the liquid fabric softener according to claim 1.
JP14350690A 1990-06-01 1990-06-01 Liquid soft finishing agent Pending JPH0441774A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14350690A JPH0441774A (en) 1990-06-01 1990-06-01 Liquid soft finishing agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14350690A JPH0441774A (en) 1990-06-01 1990-06-01 Liquid soft finishing agent

Publications (1)

Publication Number Publication Date
JPH0441774A true JPH0441774A (en) 1992-02-12

Family

ID=15340314

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14350690A Pending JPH0441774A (en) 1990-06-01 1990-06-01 Liquid soft finishing agent

Country Status (1)

Country Link
JP (1) JPH0441774A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3312336A1 (en) * 2007-06-15 2018-04-25 Ecolab Inc. Fabric conditioner composition and method of use

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3312336A1 (en) * 2007-06-15 2018-04-25 Ecolab Inc. Fabric conditioner composition and method of use
US10113139B2 (en) 2007-06-15 2018-10-30 Ecolab Usa Inc. Solid fabric conditioner composition and method of use
EP3901357A1 (en) * 2007-06-15 2021-10-27 Ecolab USA Inc. Liquid fabric conditioner composition and method of use

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