JPH0254400B2 - - Google Patents
Info
- Publication number
- JPH0254400B2 JPH0254400B2 JP6816882A JP6816882A JPH0254400B2 JP H0254400 B2 JPH0254400 B2 JP H0254400B2 JP 6816882 A JP6816882 A JP 6816882A JP 6816882 A JP6816882 A JP 6816882A JP H0254400 B2 JPH0254400 B2 JP H0254400B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- amino acid
- neutral amino
- soluble
- salt
- 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.)
- Expired
Links
- 150000003839 salts Chemical class 0.000 claims description 20
- 150000001413 amino acids Chemical class 0.000 claims description 17
- 230000007935 neutral effect Effects 0.000 claims description 17
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 14
- 239000000194 fatty acid Substances 0.000 claims description 14
- 229930195729 fatty acid Natural products 0.000 claims description 14
- 150000004665 fatty acids Chemical class 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 14
- 229910017053 inorganic salt Inorganic materials 0.000 claims description 7
- 239000003599 detergent Substances 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- 125000002252 acyl group Chemical group 0.000 claims description 5
- -1 alkanolamines Inorganic materials 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 150000001768 cations Chemical class 0.000 claims description 4
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- VDIPNVCWMXZNFY-UHFFFAOYSA-N N-methyl-beta-alanine Chemical compound CNCCC(O)=O VDIPNVCWMXZNFY-UHFFFAOYSA-N 0.000 claims description 2
- 108010077895 Sarcosine Proteins 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical group 0.000 claims description 2
- 229910021529 ammonia Inorganic materials 0.000 claims description 2
- 150000001450 anions Chemical class 0.000 claims description 2
- 229940043230 sarcosine Drugs 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 2
- 150000004670 unsaturated fatty acids Chemical group 0.000 claims description 2
- 150000008043 acidic salts Chemical class 0.000 claims 1
- 235000002639 sodium chloride Nutrition 0.000 description 18
- 238000000034 method Methods 0.000 description 7
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
- 238000005187 foaming Methods 0.000 description 4
- 230000008719 thickening Effects 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 235000019864 coconut oil Nutrition 0.000 description 3
- 239000003240 coconut oil Substances 0.000 description 3
- 239000012263 liquid product Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 239000005639 Lauric acid Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000000774 hypoallergenic effect Effects 0.000 description 2
- 239000001103 potassium chloride Substances 0.000 description 2
- 235000011164 potassium chloride Nutrition 0.000 description 2
- 239000002453 shampoo Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- 239000004475 Arginine Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000007836 KH2PO4 Substances 0.000 description 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
- 229910000396 dipotassium phosphate Inorganic materials 0.000 description 1
- 235000019797 dipotassium phosphate Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- LOBXNKKFDKXXQW-UHFFFAOYSA-M sodium;3-[dodecanoyl(methyl)amino]propanoate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CCC([O-])=O LOBXNKKFDKXXQW-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 229910000404 tripotassium phosphate Inorganic materials 0.000 description 1
- 235000019798 tripotassium phosphate Nutrition 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Description
本発明はN―アシル中性アミノ酸水溶性塩を含
有する液体洗浄剤に関するものである。
N―アシル中性アミノ酸水溶性塩は、低刺激性
であり、泡立ちにすぐれ、しかも使用後の皮膚の
感触が良好なため、近年になつてシヤンプーや皮
膚洗浄剤に多く用いられるようになつてきた。し
かし、N―アシル中性アミノ酸水溶性塩の水溶液
は粘度が低く、しかも液状製品に配合すると製品
の粘度を低下させる性質があるため、このものを
配合した液状製品を増粘することが困難であつ
た。シヤンプーや皮膚洗浄剤等の液状製品の場
合、使いやすさ商品のイメージから少なくとも
50cp程度の粘度は必要であり、N―アシル中性
アミノ酸水溶性塩を配合した液体洗浄剤は、低刺
激性で泡立ちにすぐれているものの、商品価値は
低いものであつた。
従来、N―アシル中性アミノ酸水溶性塩の水溶
液の増粘方法としては、
(1) メチルセルロース、ヒドロキシメチルセルロ
ース、ポリアクリル酸等の水溶性高分子を配合
する方法、
(2) 脂肪酸アルカノールアミドを配合する方法、
(3) 食塩や塩化カリウム等の無機塩を配合する方
法、
(4) 高級アルコールやグリコール類の脂肪酸エス
テルを配合する方法、
などが知られている。
しかし、これらの方法にはそれぞれ欠点があ
り、いずれも充分な方法とはいえない。すなわ
ち、(1)の方法は使用時ヌルヌル感があつたり、糸
を引く欠点があり、(2)、(3)、(4)の方法は適度な粘
度になるまで配合すると、耐寒性が悪くなり、さ
らに(4)の方法は泡立ちを悪くすることもある等の
欠点を有している。
本発明者らは、耐寒性や泡立ちを低下させず
に、N―アシル中性アミノ酸水溶性塩の水溶液を
増粘する方法について検討を行なつたところ、脂
肪酸ジエタノールアミドと特定の水溶性無機塩を
特定の比率で併用することにより目的が達成され
ることを見いだし、本発明を完成するに至つた。
すなわち本発明は、
a N―アシル中性アミノ酸水溶性塩:35〜
80wt%
b 脂肪酸ジエタノールアミド:5〜60wt%
c 水溶性無機塩:5〜60wt%
を必須成分(ただし、a、bおよびcの合計は
100wt%とする)とすることを特徴とする増粘性
と耐寒性の改良された液体洗浄剤組成物に関する
ものである。
本発明組成物で用いられるN―アシル中性アミ
ノ酸水溶性塩のアシル基は、炭素数10ないし18の
飽和または不飽和の脂肪酸残基からなり、たとえ
ばヤシ油脂肪酸、ラウリン酸、ミリスチン酸およ
びオレイン酸などの脂肪酸の残基をあげることが
できる。N―アシル中性アミノ酸水溶性塩の中性
アミノ酸は、ザルコシン、N―メチル―β―アラ
ニンから選ばれ、水溶性塩を形成するカチオンは
ナトリウム、カリウムなどのアルカリ金属、モノ
エタノールアミン、ジエタノールアミン、トリエ
タノールアミンなどのアルカノールアミン、リジ
ン、アルギニンなどの塩基性アミノ酸およびアン
モニアが用いられる。
本発明組成物の第2の必須成分である脂肪酸ジ
エタノールアミドのアシル基は、炭素数10ないし
18のものが用いることができる。好ましいアシル
基としては、たとえばヤシ油脂肪酸、ラウリン
酸、ミリスチン酸などの脂肪酸の残基があげられ
る。なお、脂肪酸モノエタノールアミドは増粘効
果は認められるが耐寒性が悪くなり好ましくな
い。
本発明組成物の第3の必須成分として用いられ
る水溶性無機塩は、Na+、K+、NH+ 4、からなる
陽イオンと、Cl-、SO2- 4、PO3- 4、CO2- 3からなる
陰イオンから形成される酸性塩を含む無機塩の少
なくとも1種である。これらの水溶性無機塩とし
ては、たとえばNaCl、Na2CO4、NaHSO4、
Na3PO4、Na2HPO4、KCl、K2SO4、KHSO4、
K3PO4、K2HPO4、KH2PO4、NH4Cl、
(NH4)2SO4、(NH4)3PO4、(NH4)2HPO4、
NH4H2PO4などがあげられる。
これらの水溶性無機塩は、単独または2種以上
併用してもよい。
これらの各必須成分の配合割合は、N―アシル
中性アミノ酸水溶性塩35〜80wt%、脂肪酸ジエ
タノールアミド5〜60wt%、水溶性無機塩5〜
60wt%であり、各成分の合計が100wt%になるも
のとする。この範囲外では、得られる液体洗浄剤
の粘度が低くなつたり、耐寒性が低下したりして
好ましくない。
本発明組成物において液体洗浄剤中にしめる上
記3成分の合計量の割合は、使用する目的や必須
成分の種類により異なるが、10ないし35wt%が
好ましい。10wt%以下では泡立ちや洗浄力が不
充分であり、35wt%以上では耐寒性が悪くなり
好ましくない。
本発明組成物の耐寒性と粘度を調べるため、次
のA〜Cの実験を行なつた。
実験A
N―ラウロイル―N―メチル―β―アラニンナ
トリウム塩、ヤシ油脂肪酸ジエタノールアミドお
よび塩化ナトリウムを第1図に示す割合で配合
し、3成分の合計量が25wt%になるように調製
し、クエン酸でPH7.0とした。このようにして得
られたた試料の25℃における粘度と耐寒性を測定
した。ただし、粘度は東京計器(株)製B型粘度計を
使用して測定した。耐寒性試験は、試料を−5℃
に7日間静置後の状態を観察し、次の判定に従が
つて評価した。
―耐寒性の判定基準―
〇……均一透明なもの
△……少し白濁しているもの
×……白濁または分離しているもの
測定した結果を第1表に示す。なお第1表中の
No.は、第1図の三角図表中の番号に対応するもの
である。第1表中の〇でかこまれたNo.は本発明範
囲内にある配合である。
The present invention relates to liquid detergents containing water-soluble N-acyl neutral amino acid salts. In recent years, N-acyl neutral amino acid water-soluble salts have been increasingly used in shampoos and skin cleansers because they are hypoallergenic, foam well, and leave a pleasant feeling on the skin after use. Ta. However, an aqueous solution of N-acyl neutral amino acid water-soluble salt has a low viscosity, and when added to a liquid product, it tends to reduce the viscosity of the product, so it is difficult to thicken a liquid product containing this solution. It was hot. In the case of liquid products such as shampoos and skin cleansers, at least
A viscosity of about 50 cp is required, and although liquid detergents containing N-acyl neutral amino acid water-soluble salts are hypoallergenic and have excellent foaming properties, their commercial value is low. Conventionally, methods for thickening aqueous solutions of N-acyl neutral amino acid water-soluble salts include (1) blending water-soluble polymers such as methylcellulose, hydroxymethylcellulose, and polyacrylic acid, and (2) blending fatty acid alkanolamides. (3) Adding inorganic salts such as common salt or potassium chloride; (4) Adding fatty acid esters of higher alcohols and glycols. However, each of these methods has drawbacks, and none of them can be said to be a sufficient method. In other words, method (1) has the disadvantage that it feels slimy and stringy when used, and methods (2), (3), and (4) have poor cold resistance when blended to a suitable viscosity. Furthermore, method (4) has drawbacks such as poor foaming. The present inventors investigated a method for thickening an aqueous solution of a water-soluble N-acyl neutral amino acid salt without reducing cold resistance or foaming, and found that fatty acid diethanolamide and a specific water-soluble inorganic salt The inventors have discovered that the object can be achieved by using these in combination in a specific ratio, and have completed the present invention. That is, the present invention provides a N-acyl neutral amino acid water-soluble salt: 35-
80wt% b Fatty acid diethanolamide: 5-60wt% c Water-soluble inorganic salt: 5-60wt% as essential components (however, the total of a, b and c is
The present invention relates to a liquid detergent composition with improved thickening properties and cold resistance, characterized in that the composition has a concentration of 100 wt%). The acyl group of the N-acyl neutral amino acid water-soluble salt used in the composition of the present invention consists of a saturated or unsaturated fatty acid residue having 10 to 18 carbon atoms, such as coconut oil fatty acid, lauric acid, myristic acid, and oleic acid. Examples include residues of fatty acids such as acids. The neutral amino acid of the N-acyl neutral amino acid water-soluble salt is selected from sarcosine, N-methyl-β-alanine, and the cation forming the water-soluble salt is alkali metals such as sodium and potassium, monoethanolamine, diethanolamine, Alkanolamines such as triethanolamine, basic amino acids such as lysine and arginine, and ammonia are used. The acyl group of fatty acid diethanolamide, which is the second essential component of the composition of the present invention, has 10 to 10 carbon atoms.
18 can be used. Preferred acyl groups include, for example, residues of fatty acids such as coconut oil fatty acid, lauric acid, and myristic acid. Although fatty acid monoethanolamide has a thickening effect, it has poor cold resistance and is not preferred. The water-soluble inorganic salt used as the third essential component of the composition of the present invention contains cations consisting of Na + , K + , NH + 4 , and Cl - , SO 2- 4 , PO 3- 4 , CO 2 - at least one type of inorganic salt including an acid salt formed from an anion consisting of 3 . Examples of these water-soluble inorganic salts include NaCl, Na 2 CO 4 , NaHSO 4 ,
Na 3 PO 4 , Na 2 HPO 4 , KCl, K 2 SO 4 , KHSO 4 ,
K3PO4 , K2HPO4 , KH2PO4 , NH4Cl ,
(NH 4 ) 2 SO 4 , (NH 4 ) 3 PO 4 , (NH 4 ) 2 HPO 4 ,
Examples include NH 4 H 2 PO 4 . These water-soluble inorganic salts may be used alone or in combination of two or more. The blending ratio of each of these essential components is 35 to 80 wt% N-acyl neutral amino acid water-soluble salt, 5 to 60 wt% fatty acid diethanolamide, and 5 to 5 wt% water-soluble inorganic salt.
60wt%, and the total of each component is 100wt%. Outside this range, the viscosity of the obtained liquid detergent may become low or the cold resistance may deteriorate, which is not preferable. In the composition of the present invention, the total proportion of the above three components contained in the liquid detergent varies depending on the purpose of use and the types of essential components, but is preferably 10 to 35 wt%. If it is less than 10 wt%, foaming and detergency will be insufficient, and if it is more than 35 wt%, cold resistance will be poor, which is not preferable. In order to investigate the cold resistance and viscosity of the composition of the present invention, the following experiments A to C were conducted. Experiment A N-lauroyl-N-methyl-β-alanine sodium salt, coconut oil fatty acid diethanolamide, and sodium chloride were blended in the proportions shown in Figure 1, and the total amount of the three components was adjusted to 25 wt%. The pH was adjusted to 7.0 with citric acid. The viscosity at 25°C and cold resistance of the sample thus obtained were measured. However, the viscosity was measured using a B-type viscometer manufactured by Tokyo Keiki Co., Ltd. For the cold resistance test, the sample was heated to -5°C.
The condition was observed after standing for 7 days and evaluated according to the following judgment. - Criteria for judging cold resistance - 〇... Uniformly transparent △... Slightly cloudy ×... Cloudy or separated The measurement results are shown in Table 1. In addition, in Table 1
No. corresponds to the number in the triangular diagram in FIG. The numbers circled in Table 1 are formulations within the scope of the present invention.
【表】【table】
Claims (1)
液体洗浄剤組成物において、 a N―アシル中性アミノ酸水溶性塩:35〜
80wt% b 脂肪酸ジエタノールアミド:5〜60wt% c 水溶性無機塩:5〜60wt% を必須成分(ただし、a、b、およびcの合計は
100wt%とする)とすることを特徴とする液体洗
浄剤組成物。 2 N―アシル中性アミノ酸水溶性塩の中性アミ
ノ酸が、ザルコシン、N―メチル―β―アラニン
から選ばれる特許請求の範囲第1項記載の組成
物。 3 N―アシル中性アミノ酸水溶性塩のアシル基
が、炭素数10ないし18の飽和または不飽和の脂肪
酸残基である特許請求の範囲第1項記載の組成
物。 4 N―アシル中性アミノ酸水溶性塩の水溶性塩
を形成するカチオンが、アルカリ金属、アルカノ
ールアミン、アンモニア、塩基性アミノ酸から選
ばれる特許請求の範囲第1項記載の組成物。 5 脂肪酸ジエタノールアミドのアシル基が、炭
素数10ないし18の脂肪酸残基である特許請求の範
囲第1項記載の組成物。 6 水溶性無機塩が、Na+、K+、NH4 +からなる
陽イオンと、Cl-、SO2- 4、PO3- 4、CO2- 3からなる
陰イオンから形成される酸性塩を含む無機塩の少
なくとも1種である特許請求の範囲第1項記載の
組成物。[Scope of Claims] 1 A liquid detergent composition containing a N-acyl neutral amino acid water-soluble salt, wherein a N-acyl neutral amino acid water-soluble salt: 35 to
80wt% b Fatty acid diethanolamide: 5-60wt% c Water-soluble inorganic salt: 5-60wt% as essential components (however, the total of a, b, and c is
100wt%). 2. The composition according to claim 1, wherein the neutral amino acid of the water-soluble salt of N-acyl neutral amino acid is selected from sarcosine and N-methyl-β-alanine. 3. The composition according to claim 1, wherein the acyl group of the water-soluble salt of N-acyl neutral amino acid is a saturated or unsaturated fatty acid residue having 10 to 18 carbon atoms. 4. The composition according to claim 1, wherein the cation forming the water-soluble salt of the N-acyl neutral amino acid water-soluble salt is selected from alkali metals, alkanolamines, ammonia, and basic amino acids. 5. The composition according to claim 1, wherein the acyl group of the fatty acid diethanolamide is a fatty acid residue having 10 to 18 carbon atoms. 6 Water-soluble inorganic salts are acidic salts formed from cations consisting of Na + , K + , and NH 4 + and anions consisting of Cl - , SO 2- 4 , PO 3- 4 , and CO 2- 3 . The composition according to claim 1, which contains at least one inorganic salt.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6816882A JPS58185697A (en) | 1982-04-23 | 1982-04-23 | Liquid detergent composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6816882A JPS58185697A (en) | 1982-04-23 | 1982-04-23 | Liquid detergent composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58185697A JPS58185697A (en) | 1983-10-29 |
JPH0254400B2 true JPH0254400B2 (en) | 1990-11-21 |
Family
ID=13365961
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6816882A Granted JPS58185697A (en) | 1982-04-23 | 1982-04-23 | Liquid detergent composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58185697A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5974196A (en) * | 1982-10-20 | 1984-04-26 | 花王株式会社 | Detergent composition |
JPH07116468B2 (en) * | 1986-06-26 | 1995-12-13 | ライオン株式会社 | Detergent composition for washing dishes |
JP2003048823A (en) * | 2001-08-03 | 2003-02-21 | Noevir Co Ltd | Weak-acidic skin detergent |
-
1982
- 1982-04-23 JP JP6816882A patent/JPS58185697A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS58185697A (en) | 1983-10-29 |
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