JPH07165691A - New ammonium salt and surfactant composition containing the same salt - Google Patents

New ammonium salt and surfactant composition containing the same salt

Info

Publication number
JPH07165691A
JPH07165691A JP26004294A JP26004294A JPH07165691A JP H07165691 A JPH07165691 A JP H07165691A JP 26004294 A JP26004294 A JP 26004294A JP 26004294 A JP26004294 A JP 26004294A JP H07165691 A JPH07165691 A JP H07165691A
Authority
JP
Japan
Prior art keywords
ammonium salt
hair
formula
alkyl
carbon atoms
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.)
Granted
Application number
JP26004294A
Other languages
Japanese (ja)
Other versions
JP2547313B2 (en
Inventor
Koshiro Sotodani
孝四郎 外谷
Uichiro Nishimoto
宇一郎 西本
Yoshifumi Nishimoto
吉史 西本
Osamu Tatezawa
修 立澤
Toru Kato
徹 加藤
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 JP26004294A priority Critical patent/JP2547313B2/en
Publication of JPH07165691A publication Critical patent/JPH07165691A/en
Application granted granted Critical
Publication of JP2547313B2 publication Critical patent/JP2547313B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/62Quaternary ammonium compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

PURPOSE:To obtain a new ammonium salt capable of imperting sufficient softness, antistatic property and elasticity to the fiber and excellent softness, smoothness and moistened feeling to hair in washing or drying hair. CONSTITUTION:An ammonium salt of formula I or formula II (R<1> is a 1-4C alkyl or a hydroxyalkyl; R<2> and R<3> are each an 11-21C alkyl or an alkenyl; R<4> is H or a 1-4C alkyl, with the proviso that both of two R<4>s are not H; R<5> is a 12-22C alkyl or an alkenyl; X is a halogen, a sulfate or a 1-4C alkylsulfate) and a surfactant composition containing the ammonium salt, e.g. a compound of formula III or formula IV. This compound is obtained by quaternalizing a tert-amine of formula V, etc., as a precursor with an R<4>-Y (Y is a halogen), etc., or neutralizing the tert-amine with a hydrohalogenic acid, etc.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は新規アンモニウム塩に関
し、詳しくは繊維に対して優れた柔軟性を付与し、毛髪
に対しては優れた柔軟性と平滑性を付与できるアンモニ
ウム塩及びこれを含む界面活性剤組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a novel ammonium salt, and more particularly, an ammonium salt capable of imparting excellent flexibility to fibers and excellent flexibility and smoothness to hair, and an ammonium salt containing the same. It relates to a surfactant composition.

【0002】[0002]

【従来の技術及び発明が解決しようとする課題】現在、
繊維用柔軟仕上剤又は毛髪処理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。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又は毛髪に対して良好な柔軟効果
又は平滑効果を有するからである。しかしながら、上記
の第4級アンモニウム塩は、木綿類に対しては著しい柔
軟効果を有しているが、アクリル系、ポリエステル系、
ポリアミド系等の合成繊維に対しては効果が十分とは言
いがたく、更に高濃度で処理すると衣料の弾力性が低下
し、風合いが損なわれてしまうことがある。
2. Description of the Related Art Currently,
Most of the commercially available products as a softening agent for fibers or a hair treatment agent are quaternary ammonium having two long-chain alkyl groups in one molecule as represented by di (cured tallow alkyl) dimethylammonium chloride. It is a composition whose main component is salt. The reason for this is that the quaternary ammonium salt has a good softening effect or smoothing effect on various fibers or hair in a small amount. However, although the above quaternary ammonium salt has a remarkable softening effect on cotton, it is acrylic, polyester,
It is hard to say that the effect is sufficient for synthetic fibers such as polyamide-based fibers, and if the treatment is carried out at a higher concentration, the elasticity of clothing may be reduced and the texture may be impaired.

【0003】更に、上記第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。また、特に低温で長期保存をする場
合は、増粘したりゲル状になったり、分離することがあ
る。従来、市販されている繊維用柔軟剤は、上記第4級
アンモニウム塩の他にポリオキシエチレン系の非イオン
界面活性剤、電解質及び溶剤等の添加剤を配合し、水へ
の分散性及び長期保存安定性を改良しているが、その効
果は未だ不十分であった。
Further, since the above quaternary ammonium salt has a strong hydrophobicity, when it is poured into rinsing water when the stirring force is weak, the dispersibility in water is poor and, therefore, there is a possibility that the garment may be uneven. Further, particularly when it is stored for a long period of time at a low temperature, it may thicken, form a gel, or separate. Conventionally, a commercially available softener for textiles contains polyoxyethylene-based nonionic surfactant, an additive such as an electrolyte and a solvent in addition to the above quaternary ammonium salt, and dispersibility in water and long-term Although it improved storage stability, its effect was still insufficient.

【0004】また、従来より各種アミンを柔軟基剤とす
る液体柔軟仕上剤が知られている。例えば、特開昭52−
59796 号公報にはメチルジ(硬化牛脂アルキル)アミン
のような長鎖アルキルアミンを含有する繊維に柔軟性を
付与する組成物が、特開昭58−60070 号公報にはアシル
化アルカノールアミン、水溶性第4級アンモニウム塩及
び脂肪酸エステルを含有する繊維に平滑性、快適な手触
りを与える繊維材料仕上剤が、特開昭61−167083号公報
には第4級アンモニウム化合物、高級脂肪酸とヒドロキ
シ低級アルキルポリアミンとの縮合反応物及びアルキル
アミンポリグリコールエーテルを含有する分散性の良い
柔軟剤が、特開昭61−275474号公報にはジ(高級アルキ
ル)環式アミン及びブレンステッド酸を含有する繊維処
理用の安定な水性分散液が、特開昭64−85368 号公報に
はジ長鎖アルキルアミン−陰イオン性界面活性剤イオン
複合体、非シリコーンロウ及び液体担体を含む柔軟化組
成物が、特開平2−6662号公報にはヒドロキシ低級アル
キルアルキレンジアミンと高級脂肪酸の縮合物等のアミ
ン及び両性の布地コンディショニング剤を含有する布地
コンディショニング組成物が、特開平2−14076 号公報
にはジ長鎖アルキルアミン−多官能カルボン酸錯体を含
有する柔軟性、帯電防止性を付与する布類コンディショ
ニング組成物が記載されている。更に、特開昭52−5394
号公報にはモノ又はジアルキルアルキレンジアミン静電
気抑制剤及び第4級アンモニウム系柔軟剤を含有する布
類状態調節組成物が記載されている。しかしながら、こ
れらアミンを含有する柔軟剤は分散性、保存安定性は第
4級アンモニウム塩を含有する柔軟剤に比べ比較的良い
が、柔軟性能は十分でなかった。
Further, liquid softening finishes having various amines as softening bases have been conventionally known. For example, Japanese Patent Laid-Open No. 52-
59796 discloses a composition for imparting flexibility to a fiber containing a long-chain alkylamine such as methyldi (cured tallow alkyl) amine, and JP-A-58-6070 discloses an acylated alkanolamine, a water-soluble composition. A fiber material finishing agent that imparts smoothness and comfortable feel to a fiber containing a quaternary ammonium salt and a fatty acid ester is disclosed in JP-A-61-167083. Quaternary ammonium compound, higher fatty acid and hydroxy lower alkyl polyamine. A softening agent containing a condensation reaction product with an alkylamine polyglycol ether and having good dispersibility is disclosed in Japanese Patent Laid-Open No. 275474/1986 for treating fibers containing a di (higher alkyl) cyclic amine and a Bronsted acid. A stable aqueous dispersion of JP-A-64-85368 discloses a di-long chain alkylamine-anionic surfactant ionic complex, a non-silicone wax and JP-A-2-6662 discloses a fabric conditioning composition containing an amine such as a condensate of hydroxy lower alkylalkylene diamine and a higher fatty acid and an amphoteric fabric conditioning agent. 2-14076 describes a fabric conditioning composition containing a dilong-chain alkylamine-polyfunctional carboxylic acid complex, which imparts flexibility and antistatic properties. Furthermore, JP-A-52-5394
The publication describes a fabric conditioning composition containing a mono or dialkyl alkylenediamine static suppressant and a quaternary ammonium softener. However, the softening agents containing these amines have relatively good dispersibility and storage stability as compared with the softening agents containing the quaternary ammonium salt, but the softening performance was not sufficient.

【0005】更に、一般に毛髪用処理剤は、カチオン活
性剤を非イオン乳化剤又は脂肪族アルコールと一緒に水
溶性溶液又は懸濁液の形で使用し、毛髪に使用後、毛髪
と毛髪又は毛髪とブラシ間の摩擦の減少による湿潤時の
くし通り性を改良し、更に一連の特別な性質、例えば光
沢、静電気防止及び乾燥時のくし通り性を向上させてい
る。この目的のため、ジ長鎖アルキルアンモニウム塩、
例えばジステアリルジメチルアンモニウムクロライド、
ジ(硬化牛脂アルキル)ジメチルアンモニウム塩などが
使用されてきた。しかしながら、これらの第4級アンモ
ニウム塩では、毛髪の洗髪時及び乾燥時の両方の柔軟
性、平滑性、油性感をすべて満足するものはなかった。
Furthermore, in general, a hair treatment agent uses a cationic active agent in the form of an aqueous solution or suspension together with a nonionic emulsifier or an aliphatic alcohol, and after the application to the hair, the hair and the hair or the hair are treated. It improves combability when wet by reducing friction between the brushes and also enhances a series of special properties such as gloss, antistatic and combability when dry. To this end, dilong-chain alkyl ammonium salts,
For example, distearyl dimethyl ammonium chloride,
Di (hardened tallow alkyl) dimethylammonium salt and the like have been used. However, none of these quaternary ammonium salts satisfies the softness, smoothness, and oily feel of the hair both during washing and drying.

【0006】従って、本発明の課題は、繊維に対して極
めて良好な柔軟性を付与し、毛髪に対して極めて良好な
柔軟性、平滑性等を付与するアンモニウム塩及びこれを
含有する界面活性剤組成物を提供することにある。
Therefore, an object of the present invention is to provide an ammonium salt that imparts extremely good flexibility to fibers and extremely good flexibility and smoothness to hair, and a surfactant containing the same. To provide a composition.

【0007】[0007]

【課題を解決するための手段】本発明者らは、上記課題
を解決するために鋭意検討した結果、新規な特定のアン
モニウム塩が、繊維に対しては柔軟性に優れしかも衣類
に弾力性(ふっくら感)を付与でき、毛髪に対しては乾
燥時に十分な柔軟性と洗髪時、乾燥時にも平滑性を与え
ることを見出し、本発明を完成するに至った。即ち、本
発明は、下記一般式(A) 又は(B) で表されるアンモニウ
ム塩、及びこれを含有する界面活性剤組成物を提供する
ものである。
Means for Solving the Problems As a result of intensive studies for solving the above problems, the present inventors have found that a novel specific ammonium salt has excellent flexibility for fibers and elasticity for clothing ( It has been found that it can impart a fluffy feeling to the hair, and that it imparts sufficient flexibility to hair during drying and smoothness during washing and drying. That is, the present invention provides an ammonium salt represented by the following general formula (A) or (B), and a surfactant composition containing the same.

【0008】[0008]

【化3】 [Chemical 3]

【0009】〔式中、R2,R3;炭素数11〜21の直鎖又は
分岐鎖のアルキル基又はアルケニル基を示す。R4;H 又
は炭素数1〜4のアルキル基を示す。但し、2個のR4
双方共、H である場合を除く。X ;ハロゲン原子、サル
フェート又は炭素数1〜4のアルキルサルフェートを示
す。〕
[In the formula, R 2 and R 3 represent a linear or branched alkyl group or alkenyl group having 11 to 21 carbon atoms. R 4 ; H or an alkyl group having 1 to 4 carbon atoms is shown. However, the case where both two R 4 are H is excluded. X represents a halogen atom, a sulfate or an alkyl sulfate having 1 to 4 carbon atoms. ]

【0010】[0010]

【化4】 [Chemical 4]

【0011】〔式中、R1;炭素数1〜4のアルキル基又
はヒドロキシアルキル基を示す。R3;炭素数11〜21の直
鎖又は分岐鎖のアルキル基又はアルケニル基を示す。
R4;H 又は炭素数1〜4のアルキル基を示す。R5;炭素
数12〜22の直鎖又は分岐鎖のアルキル基又はアルケニル
基を示す。X ;ハロゲン原子、サルフェート又は炭素数
1〜4のアルキルサルフェートを示す。〕 本発明が提供するアンモニウム塩において、具体例とし
て例えば、次の化合物が挙げられる。
[In the formula, R 1 represents an alkyl group or a hydroxyalkyl group having 1 to 4 carbon atoms. R 3 represents a linear or branched alkyl group or alkenyl group having 11 to 21 carbon atoms.
R 4 ; H or an alkyl group having 1 to 4 carbon atoms is shown. R 5 represents a linear or branched alkyl group or alkenyl group having 12 to 22 carbon atoms. X represents a halogen atom, a sulfate or an alkyl sulfate having 1 to 4 carbon atoms. In the ammonium salt provided by the present invention, specific examples include the following compounds.

【0012】[0012]

【化5】 [Chemical 5]

【0013】これらの化合物は、前駆体である下記式
(A')又は(B')で表される3級アミンを通常の方法、すな
わちR4−Y(式中、Y はハロゲン原子を示す。)或いは(R
4)2SO4で4級化するか、あるいはハロゲン化水素酸又は
硫酸で中和することで得ることができる。
These compounds are precursors of the following formula
The tertiary amine represented by (A ′) or (B ′) can be prepared by a conventional method, that is, R 4 —Y (wherein Y represents a halogen atom) or (R
4 ) It can be obtained by quaternization with 2 SO 4 or neutralization with hydrohalic acid or sulfuric acid.

【0014】[0014]

【化6】 [Chemical 6]

【0015】〔式中のR1〜R5は前記と同じ意味を示
す。〕 上記化合物のうち、式(A')で表される化合物は、 N−低
級アルキルジエタノールアミンの分子内脱水素環化反応
により得られる下式(A−1)
[In the formula, R 1 to R 5 have the same meanings as described above. Among the above compounds, the compound represented by the formula (A ′) is a compound represented by the following formula (A-1) obtained by an intramolecular dehydrocyclization reaction of N-lower alkyldiethanolamine:

【0016】[0016]

【化7】 [Chemical 7]

【0017】〔式中、R4は前記と同じ意味を示す。〕で
表される化合物を脂肪族アミンと開環アミド化反応させ
た後、その反応生成物と炭素数12〜22の脂肪酸ハライド
とを反応させることにより得ることができる。更に式
(B')で表される化合物は N−長鎖アルキル又はアルケニ
ルジエタノールアミンの分子内脱水素環化反応により得
られる下式(B−1)
[In the formula, R 4 has the same meaning as described above. ] The compound represented by the above can be obtained by subjecting the compound to a ring-opening amidation reaction with an aliphatic amine and then reacting the reaction product with a fatty acid halide having 12 to 22 carbon atoms. Further formula
The compound represented by (B ') is represented by the following formula (B-1) obtained by the intramolecular dehydrocyclization reaction of N-long-chain alkyl or alkenyldiethanolamine.

【0018】[0018]

【化8】 [Chemical 8]

【0019】〔式中、R5は前記と同じ意味を示す。〕で
表される化合物を低級アルキルアミンと反応させた後、
その反応生成物と炭素数12〜22の脂肪酸ハライドとを反
応させることにより得ることができる。式(A')又は(B')
で表される化合物より本発明の式(A) 又は(B) で表され
るアンモニウム塩を得るためには、低級アルキルハライ
ドやジ低級アルキル硫酸等を用いた公知の方法を用いる
ことができる。また、中和物は式 (A') 又は(B')で表さ
れる化合物を酸水溶液中に投入するか、酸と同時に水へ
投入して得ることができる。
[In the formula, R 5 has the same meaning as described above. ] After reacting the compound represented by
It can be obtained by reacting the reaction product with a fatty acid halide having 12 to 22 carbon atoms. Formula (A ') or (B')
In order to obtain the ammonium salt represented by the formula (A) or (B) of the present invention from the compound represented by, a known method using a lower alkyl halide or dilower alkylsulfate can be used. The neutralized product can be obtained by adding the compound represented by the formula (A ′) or (B ′) to the aqueous acid solution, or by adding the compound to water at the same time as the acid.

【0020】本発明に係る新規アンモニウム塩を用いて
繊維用柔軟仕上剤を製品化する際、製品の粘性及びハン
ドリング性を考慮すると本発明に係る新規アンモニウム
塩の総量は4〜40重量%、好ましくは6〜30重量%、特
に好ましくは10〜30重量%である。さらに、この新規ア
ンモニウム塩は、従来公知のジ(長鎖アルキル)第4級
アンモニウム塩と併用してもよい。
When a softening agent for fibers is manufactured using the novel ammonium salt according to the present invention, the total amount of the novel ammonium salt according to the present invention is preferably 4 to 40% by weight, considering the viscosity and handling property of the product. Is 6 to 30% by weight, particularly preferably 10 to 30% by weight. Furthermore, this novel ammonium salt may be used in combination with a conventionally known di (long-chain alkyl) quaternary ammonium salt.

【0021】また、繊維用柔軟仕上剤中に、更にジメチ
ルポリシロキサン、部分的にアミノ基又はポリオキシア
ルキレン基で変性されたジメチルポリシロキサン等のシ
リコーン化合物、特に好ましくは部分的にポロオキシア
ルキレン基で変性されたジメチルポリシロキサンを配合
することによりさらに肌ざわりを改良できる。これらの
シリコーン化合物は本発明に係わる新規アンモニウム塩
の総量に対し 0.3〜5重量%配合されるのが好ましい。
本発明の新規アンモニウム塩を用いた繊維用柔軟仕上剤
は、従来広く用いられているジ(硬化牛脂アルキル)ジ
メチルアンモニウムクロライドに比較すると柔軟効果は
ほぼ同等であるが、驚くべきことに弾力性のある柔かさ
が得られることが分かった。
Further, in the softening agent for fibers, a silicone compound such as dimethylpolysiloxane, dimethylpolysiloxane partially modified with an amino group or a polyoxyalkylene group, particularly preferably a partially poloxyalkylene group. By blending dimethylpolysiloxane modified with, the skin feel can be further improved. These silicone compounds are preferably added in an amount of 0.3 to 5% by weight based on the total amount of the novel ammonium salt according to the present invention.
The softening agent for fibers using the novel ammonium salt of the present invention has almost the same softening effect as that of the widely used di (cured tallow alkyl) dimethylammonium chloride, but surprisingly has elasticity. It turns out that a certain softness can be obtained.

【0022】本発明のアンモニウム塩を水系液体繊維用
柔軟仕上剤とする際には、粘度調整のために塩化ナトリ
ウム、塩化カルシウム、塩化マグネシウム等の無機電解
質を0.05〜0.4 重量%添加するのが望ましい。また、長
期保存での高度な安定性を得るために、ポリオキシエチ
レンアルキルエーテルやポリオキシエチレンアルキルア
ミン等のノニオン活性剤、エタノール、イソプロパノー
ル、プロピレングリコールやエチレングリコールのよう
な溶剤又は尿素などを配合することができる。また、柔
軟基剤として既知のエステル、非イオンあるいはカチオ
ン化合物、長鎖アルコール等を併用してもよい。
When the ammonium salt of the present invention is used as a softening finish for aqueous liquid fibers, it is desirable to add 0.05 to 0.4% by weight of an inorganic electrolyte such as sodium chloride, calcium chloride or magnesium chloride for viscosity adjustment. . Also, in order to obtain a high degree of stability during long-term storage, nonionic activators such as polyoxyethylene alkyl ether and polyoxyethylene alkylamine, ethanol, isopropanol, solvents such as propylene glycol and ethylene glycol, or urea are added. can do. Also, known esters, nonionic or cationic compounds, long-chain alcohols, etc. may be used in combination as the softening base.

【0023】また、本発明に係わる新規アンモニウム塩
を毛髪処理剤として使用する場合は、本発明に係わる新
規アンモニウム塩の配合量は、従来使用されている第4
級アンモニウム化合物を使用する場合と同じ量でよく、
0.1〜20重量%が好ましく、更に好ましくは 0.1〜10重
量%である。本発明の新規アンモニウム塩を用いた毛髪
処理剤を使用した場合、従来使用されている第4級アン
モニウム塩を使用した毛髪処理剤と比べ湿潤時及び乾燥
時共に毛髪に対し極めて優れた柔軟性や平滑性、油っぽ
さのないしっとり感を与える。本発明の新規アンモニウ
ム塩を使用した毛髪処理剤の剤型としては、ヘアリン
ス、ヘアコンディショナー、ヘアトリートメント、ヘア
パック、ヘアクリーム、スタイリングローション、スタ
イリングムース、コンディショニングムース、ヘアムー
ス、ヘアスプレー等が挙げられる。更に、これらの毛髪
処理剤を構成する併用成分としては、従来型のモノ若し
くはジ(長鎖アルキル)第4級アンモニウム塩の様なカ
チオン活性剤やノニオン活性剤、高級アルコール、高級
エステル、炭化水素、脂肪酸、シリコンオイルなどの油
類、グリセリン、尿素などの保湿剤、カチオン性ポリマ
ー、高分子多糖類、ポリペプタイドなどの高分子物質、
低級アルコール、プロピレングリコール、ジエチレング
リコールなどの溶剤を本発明の新規アンモニウム塩の効
果を損なわない範囲で用いることができる。
When the novel ammonium salt according to the present invention is used as a hair treatment agent, the compounding amount of the novel ammonium salt according to the present invention is 4
The same amount as when using a primary ammonium compound,
The amount is preferably 0.1 to 20% by weight, more preferably 0.1 to 10% by weight. When the hair treatment agent using the novel ammonium salt of the present invention is used, compared to the hair treatment agent using a quaternary ammonium salt which has been conventionally used, the hair has excellent flexibility and wetness both in wet and dry conditions. Gives a smooth, oily or moist feeling. Examples of the dosage form of the hair treatment agent using the novel ammonium salt of the present invention include hair rinse, hair conditioner, hair treatment, hair pack, hair cream, styling lotion, styling mousse, conditioning mousse, hair mousse, and hair spray. Further, as a combined component constituting these hair treatment agents, cationic activators such as conventional mono- or di (long-chain alkyl) quaternary ammonium salts, nonionic activators, higher alcohols, higher esters, hydrocarbons, etc. , Fatty acids, oils such as silicone oil, humectants such as glycerin and urea, cationic polymers, polymeric polysaccharides, polymeric substances such as polypeptide,
Solvents such as lower alcohols, propylene glycol and diethylene glycol can be used as long as the effects of the novel ammonium salt of the present invention are not impaired.

【0024】[0024]

【実施例】次に本発明を実施例をもって詳細に説明する
が、本発明はこれら実施例に限定されるものではない。
EXAMPLES The present invention will now be described in detail with reference to examples, but the present invention is not limited to these examples.

【0025】実施例1 特願平3−20709 号の実施例2の方法を用いて、 N−メ
チルモルフォロンの合成を行った。すなわち、触媒とし
てCu:Ni:Pd=5:1:0.01組成の触媒を用い、 N−メ
チルジエタノールアミンの脱水素環化反応を行い目的物
である N−メチルモルフォロンを得た。攪拌機、温度計
のついた4つ口フラスコに N−メチルモルフォロン 115
gとステアリルアミン 269gを仕込み、 100℃まで昇温
し、その温度で2時間反応させた。得られた生成物に更
にアセトンを350g加え、ステアリン酸クロライド303.5
gを攪拌しながら滴下した。白色沈澱物が目的物である
下記構造式(1) で表される化合物であり、アセトンを濾
過にて除去し乾燥後 560gを得た。NMR 、IRスペクトル
から以下の構造を確認した。
Example 1 N-methylmorpholone was synthesized by the method of Example 2 of Japanese Patent Application No. 3-20709. That is, using a catalyst having a composition of Cu: Ni: Pd = 5: 1: 0.01 as a catalyst, a dehydrocyclization reaction of N-methyldiethanolamine was performed to obtain N-methylmorpholone which was a target product. N-methylmorpholone 115
g and stearylamine 269 g were charged, the temperature was raised to 100 ° C., and the reaction was carried out at that temperature for 2 hours. To the product obtained, 350 g of acetone was added, and stearic acid chloride 303.5 was added.
g was added dropwise with stirring. The white precipitate is the target compound represented by the following structural formula (1), and acetone was removed by filtration to obtain 560 g after drying. The following structures were confirmed from NMR and IR spectra.

【0026】[0026]

【化9】 [Chemical 9]

【0027】IRスペクトル(KBr 錠剤) 1745cm-1,1675cm-1,1475cm-1,1158cm-1 実施例2 実施例1と同様な方法で、 N−ステアリルジエタノール
アミンを原料に用いて、 N−ステアリルモルフォロンを
得た。N −ステアリルモルフォロンを 353gとブチルア
ミン73gを、攪拌機、温度計、圧力計のついたオートク
レーブに仕込み、 100℃に昇温し、その温度で2時間反
応した。その生成物を攪拌機、温度計、冷却管のついた
4つ口フラスコに 400gと、溶媒としてアセトン 800g
を仕込んだ。50℃に昇温し、ここにステアリルクロライ
ド 285gと48%NaOH78gを同時に滴下し反応を行った。
この温度で3時間熟成後、生成したNaClを濾過で除去
し、残りの生成物をオートクレーブに移し、メチルクロ
ライド57gを圧入した。 100℃で約8時間反応した後、
取り出した。白色沈澱物を濾過し、乾燥後目的物である
下記構造式(2) で表される化合物を605 g得た。NMR 、
IRスペクトルから以下の構造を確認した。
IR spectrum (KBr tablets) 1745 cm -1 , 1675 cm -1 , 1475 cm -1 , 1158 cm -1 Example 2 In the same manner as in Example 1, N-stearyl diethanolamine was used as a raw material, and N-stearylmorpho Got Ron. 353 g of N-stearylmorpholone and 73 g of butylamine were charged into an autoclave equipped with a stirrer, a thermometer and a pressure gauge, the temperature was raised to 100 ° C., and the reaction was carried out at that temperature for 2 hours. 400 g of the product in a four-necked flask equipped with a stirrer, a thermometer, and a condenser, and 800 g of acetone as a solvent.
Was charged. The temperature was raised to 50 ° C., and 285 g of stearyl chloride and 78 g of 48% NaOH were simultaneously added dropwise thereto to carry out a reaction.
After aging at this temperature for 3 hours, the produced NaCl was removed by filtration, the remaining product was transferred to an autoclave, and 57 g of methyl chloride was injected under pressure. After reacting at 100 ℃ for about 8 hours,
I took it out. The white precipitate was filtered and dried to obtain 605 g of the target compound represented by the following structural formula (2). NMR,
The following structure was confirmed from the IR spectrum.

【0028】[0028]

【化10】 [Chemical 10]

【0029】IRスペクトル(KBr 錠剤) 1735cm-1,1673cm-1,1473cm-1,1160cm-1 試験例1 繊維用柔軟剤 本発明の新規アンモニウム塩について、以下の方法によ
り柔軟性、弾力性の評価を行った。
IR spectrum (KBr tablets) 1735 cm -1 , 1673 cm -1 , 1473 cm -1 , 1160 cm -1 Test Example 1 Softener for textiles The novel ammonium salt of the present invention was evaluated for flexibility and elasticity by the following methods. I went.

【0030】<柔軟性、弾力性の評価> (1) 処理方法 市販の木綿タオル2kg、アクリルジャージ1kgを 3.5°
DH硬水にて市販洗剤アタック(花王(株)製、登録商
標)にて5回繰り返し洗濯(30リットル洗濯機)をし、
各繊維についていた繊維処理剤を除去した後、表1の配
合組成物を有効成分として 1.5gを投入し、25℃、1分
間攪拌下で処理した。なおいずれの配合の場合もポリオ
キシエチレン変性ジメチルポリシロキサンを本発明に係
わる化合物総量に対して1重量%配合した。
<Evaluation of flexibility and elasticity> (1) Treatment method Commercially available cotton towel 2 kg, acrylic jersey 1 kg 3.5 °
Repeatedly wash 5 times (30 liter washing machine) with commercial detergent attack (registered trademark, manufactured by Kao Corporation) with DH hard water,
After removing the fiber treating agent attached to each fiber, 1.5 g of the compounded composition of Table 1 was added as an active ingredient and treated under stirring at 25 ° C. for 1 minute. In each case, 1% by weight of polyoxyethylene-modified dimethylpolysiloxane was added to the total amount of the compounds according to the present invention.

【0031】(2) 評価方法 上記方法で処理した布を室温で風乾後、25℃、65%RHの
恒温恒湿にて24時間放置した。これらの布について柔軟
性、弾力性の評価を行った。柔軟性及び弾力性の評価
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。 +2;対照より柔らかい又は弾力性が高い +1;対照よりやや柔らかい又は弾力性がやや高い 0;対照と同じ −1;対照の方がやや柔らかい又は対照より弾力性がや
や低い −2;対照の方が柔らかい又は対照より弾力性が低い また比較品として用いた化合物(D) 、(E) を以下に示
す。 (D) ;ジステアリルジメチルアンモニウムクロライド
(2) Evaluation method The cloth treated by the above method was air-dried at room temperature, and then allowed to stand for 24 hours at a constant temperature and humidity of 25 ° C. and 65% RH. The softness and elasticity of these cloths were evaluated. For the evaluation of softness and elasticity, pairwise comparison was carried out by using a cloth treated with 10 cc of a softening agent containing 15% by weight of di (hardened beef tallow alkyl) dimethylammonium chloride as a control. The evaluation is expressed as follows. +2; softer or more elastic than the control +1; slightly softer or more elastic than the control 0; same as the control -1; slightly softer than the control or slightly less elastic than the control -2: the control Is softer or less elastic than the control. The compounds (D) and (E) used as comparative products are shown below. (D) ; Distearyl dimethyl ammonium chloride

【0032】[0032]

【化11】 [Chemical 11]

【0033】[0033]

【表1】 [Table 1]

【0034】表1に示すように、本発明の化合物を使用
することにより、繊維に対する柔軟性と弾力性の付与効
果において双方を満足する結果が得られた。
As shown in Table 1, by using the compound of the present invention, the results that satisfy both the effect of imparting flexibility and elasticity to the fiber were obtained.

【0035】試験例2 毛髪用処理剤 本発明の新規アンモニウム塩について毛髪処理剤として
の効果を、以下の組成で調べた。 <組成> アンモニウム塩 1% (本発明のアンモニウム塩又は対照化合物(D)) オクタデシルトリメチルアンモニウムクロライド 1% セチルアルコール 3% 水 バランス 上記の組成の毛髪リンス組成物を毛束に対し、それぞれ
10%塗布し、塗布後3分間放置した後、30℃の温水で一
定時間すすぎ、タオルドライをしてWET時の髪の評価
を行った。その後、ドライヤーで毛束を乾燥し、DRY
時の髪の評価を行った。評価は10人のパネラーにより、
手による触感で行い、下記の基準で評価した。この結果
を表2にまとめて示した。
Test Example 2 Hair Treatment Agent The effect of the novel ammonium salt of the present invention as a hair treatment agent was examined with the following composition. <Composition> Ammonium salt 1% (ammonium salt of the present invention or control compound (D)) Octadecyltrimethylammonium chloride 1% Cetyl alcohol 3% Water balance The hair rinse composition having the above composition is applied to each hair bundle.
After applying 10% and leaving for 3 minutes after application, the hair was rinsed with warm water at 30 ° C. for a certain period of time, towel-dried, and the hair at WET was evaluated. After that, the hair bundle is dried with a dryer and DRY
The hair at that time was evaluated. Evaluation is by 10 panelists,
It was touched by the hand and evaluated according to the following criteria. The results are summarized in Table 2.

【0036】<柔軟性> 3:やわらかい感じがする 2:やわらかい感じが不足する 1:やわらかい感じに欠ける <平滑性> 3:すべすべする 2:ややすべすべしない 1:すべすべしない <しっとり感> 3:しっとりする 2:ややしっとりしない 1:しっとりしない <油性感> 3:べとつきがない 2:ややべとつく 1:べとつく<Flexibility> 3: Feeling soft 2: Lacking softness 1: Lacking softness <Smoothness> 3: Smooth 2: No smoothness 1: Non-smooth <Moisture> 3: Moisture Yes 2: Somewhat moist 1: No moist <oiliness> 3: No stickiness 2: Some stickiness 1: Sticky

【0037】[0037]

【表2】 [Table 2]

【0038】以上のように、本発明のアンモニウム塩を
用いた場合には、毛髪の洗髪時及び乾燥時の両方におい
て、柔軟性、平滑性、しっとり感、油性感のすべてにお
いて、きわめて優れた効果を示すことがわかった。
As described above, when the ammonium salt of the present invention is used, a very excellent effect is obtained in all of the softness, smoothness, moisturizing feeling and oily feeling both during washing and drying of hair. Was found to show.

【0039】[0039]

【発明の効果】本発明の新規アンモニウム塩は、柔軟仕
上剤として用いた場合、各繊維に対して十分な柔軟性、
帯電防止性を与え、且つ優れた弾力性を付与する。ま
た、毛髪処理剤として使用した場合、毛髪の洗髪時及び
乾燥時の両方において、柔軟性、平滑性、油っぽさのな
いしっとり感において極めて優れた効果を付与する。
The novel ammonium salt of the present invention, when used as a softening agent, has sufficient flexibility for each fiber,
It provides antistatic properties and excellent elasticity. Further, when used as a hair treatment agent, it imparts an extremely excellent effect in terms of flexibility, smoothness, and oily or moisturizing feeling both when washing and drying hair.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 下記一般式(A) で表されるアンモニウム
塩。 【化1】 〔式中、R2,R3;炭素数11〜21の直鎖又は分岐鎖のアル
キル基又はアルケニル基を示す。R4;H 又は炭素数1〜
4のアルキル基を示す。但し、2個のR4が双方共、H で
ある場合を除く。X ;ハロゲン原子、サルフェート又は
炭素数1〜4のアルキルサルフェートを示す。〕
1. An ammonium salt represented by the following general formula (A): [Chemical 1] [In the formula, R 2 and R 3 represent a linear or branched alkyl group or alkenyl group having 11 to 21 carbon atoms. R 4 ; H or 1 to 1 carbon atoms
4 represents an alkyl group. However, the case where both two R 4 are H is excluded. X represents a halogen atom, a sulfate or an alkyl sulfate having 1 to 4 carbon atoms. ]
【請求項2】 下記一般式(B) で表されるアンモニウム
塩。 【化2】 〔式中、R1;炭素数1〜4のアルキル基又はヒドロキシ
アルキル基を示す。R3;炭素数11〜21の直鎖又は分岐鎖
のアルキル基又はアルケニル基を示す。R4;H 又は炭素
数1〜4のアルキル基を示す。R5;炭素数12〜22の直鎖
又は分岐鎖のアルキル基又はアルケニル基を示す。X ;
ハロゲン原子、サルフェート又は炭素数1〜4のアルキ
ルサルフェートを示す。〕
2. An ammonium salt represented by the following general formula (B): [Chemical 2] Wherein, R 1; represents an alkyl group or hydroxyalkyl group having 1 to 4 carbon atoms. R 3 represents a linear or branched alkyl group or alkenyl group having 11 to 21 carbon atoms. R 4 ; H or an alkyl group having 1 to 4 carbon atoms is shown. R 5 represents a linear or branched alkyl group or alkenyl group having 12 to 22 carbon atoms. X ;
A halogen atom, a sulfate, or an alkyl sulfate having 1 to 4 carbon atoms is shown. ]
【請求項3】 請求項1又は2記載のアンモニウム塩を
含有する界面活性剤組成物。
3. A surfactant composition containing the ammonium salt according to claim 1.
JP26004294A 1994-10-25 1994-10-25 Novel ammonium salt and surfactant composition containing the same Expired - Fee Related JP2547313B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26004294A JP2547313B2 (en) 1994-10-25 1994-10-25 Novel ammonium salt and surfactant composition containing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26004294A JP2547313B2 (en) 1994-10-25 1994-10-25 Novel ammonium salt and surfactant composition containing the same

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP4031818A Division JPH0749402B2 (en) 1992-02-19 1992-02-19 Novel ammonium salt and surfactant composition containing the same

Publications (2)

Publication Number Publication Date
JPH07165691A true JPH07165691A (en) 1995-06-27
JP2547313B2 JP2547313B2 (en) 1996-10-23

Family

ID=17342500

Family Applications (1)

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Country Link
JP (1) JP2547313B2 (en)

Also Published As

Publication number Publication date
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