JPS6129322B2 - - Google Patents

Info

Publication number: JPS6129322B2
Authority: JP; Japan
Prior art keywords: amino acid; salt; equimolar; arginine; basic amino
Prior art date: 1980-05-02
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

Application number

JP55059038A

Other languages

English (en)

Japanese (ja)

Other versions

JPS56155298A (en

Inventor

Kazuharu Shiraki

Kazuki Fujii

Hidefumi Fujita

Nakami Fukuda

Norio Sugihara

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.)

Tanabe Seiyaku Co Ltd

Original Assignee

Tanabe Seiyaku Co Ltd

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.)

1980-05-02

Filing date

1980-05-02

Publication date

1986-07-05

1980-05-02 Application filed by Tanabe Seiyaku Co Ltd filed Critical Tanabe Seiyaku Co Ltd

1980-05-02 Priority to JP5903880A priority Critical patent/JPS56155298A/ja

1981-12-01 Publication of JPS56155298A publication Critical patent/JPS56155298A/ja

1986-07-05 Publication of JPS6129322B2 publication Critical patent/JPS6129322B2/ja

Status Granted legal-status Critical Current

Links

239000000203 mixture Substances 0.000 claims description 57
235000001014 amino acid Nutrition 0.000 claims description 55
239000002453 shampoo Substances 0.000 claims description 42
-1 amino acid salts Chemical class 0.000 claims description 41
150000003839 salts Chemical class 0.000 claims description 40
150000001413 amino acids Chemical class 0.000 claims description 37
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 14
230000002378 acidificating effect Effects 0.000 claims description 14
125000002252 acyl group Chemical group 0.000 claims description 14
125000001931 aliphatic group Chemical group 0.000 claims description 14
239000011593 sulfur Substances 0.000 claims description 14
229910052717 sulfur Inorganic materials 0.000 claims description 14
239000004475 Arginine Substances 0.000 claims description 12
ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims description 9
239000004472 Lysine Substances 0.000 claims description 7
WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 claims description 5
CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims description 5
KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims description 5
235000003704 aspartic acid Nutrition 0.000 claims description 5
OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 claims description 5
235000013922 glutamic acid Nutrition 0.000 claims description 5
239000004220 glutamic acid Substances 0.000 claims description 5
PWKSKIMOESPYIA-BYPYZUCNSA-N L-N-acetyl-Cysteine Chemical compound CC(=O)N[C@@H](CS)C(O)=O PWKSKIMOESPYIA-BYPYZUCNSA-N 0.000 claims description 4
229960004308 acetylcysteine Drugs 0.000 claims description 3
238000002156 mixing Methods 0.000 claims description 3
XUYPXLNMDZIRQH-LURJTMIESA-N N-acetyl-L-methionine Chemical compound CSCC[C@@H](C(O)=O)NC(C)=O XUYPXLNMDZIRQH-LURJTMIESA-N 0.000 claims description 2
229940099459 n-acetylmethionine Drugs 0.000 claims description 2
238000009472 formulation Methods 0.000 description 23
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
239000008213 purified water Substances 0.000 description 20
239000003086 colorant Substances 0.000 description 16
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 12
239000003205 fragrance Substances 0.000 description 12
229940055577 oleyl alcohol Drugs 0.000 description 12
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 12
235000014113 dietary fatty acids Nutrition 0.000 description 11
229930195729 fatty acid Natural products 0.000 description 11
239000000194 fatty acid Substances 0.000 description 11
150000004665 fatty acids Chemical class 0.000 description 11
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 10
SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 10
KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 10
239000011734 sodium Substances 0.000 description 10
229910052708 sodium Inorganic materials 0.000 description 10
AXISYYRBXTVTFY-UHFFFAOYSA-N Isopropyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OC(C)C AXISYYRBXTVTFY-UHFFFAOYSA-N 0.000 description 9
235000019864 coconut oil Nutrition 0.000 description 8
239000003240 coconut oil Substances 0.000 description 8
HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 7
JZKFHQMONDVVNF-UHFFFAOYSA-N dodecyl sulfate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCCCCCCOS(O)(=O)=O JZKFHQMONDVVNF-UHFFFAOYSA-N 0.000 description 6
210000004761 scalp Anatomy 0.000 description 6
SUUWYOYAXFUOLX-ZBRNBAAYSA-N (2s)-2-aminobutanedioic acid;(2s)-2-amino-5-(diaminomethylideneamino)pentanoic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O.OC(=O)[C@@H](N)CCCN=C(N)N SUUWYOYAXFUOLX-ZBRNBAAYSA-N 0.000 description 5
229960003237 betaine Drugs 0.000 description 5
VNUREHWOFQRPGE-UHFFFAOYSA-N 2-[2-dodecyl-1-(2-hydroxyethyl)-4,5-dihydroimidazol-1-ium-1-yl]acetate Chemical compound CCCCCCCCCCCCC1=NCC[N+]1(CCO)CC([O-])=O VNUREHWOFQRPGE-UHFFFAOYSA-N 0.000 description 4
230000003750 conditioning effect Effects 0.000 description 4
239000000796 flavoring agent Substances 0.000 description 4
235000019634 flavors Nutrition 0.000 description 4
238000003756 stirring Methods 0.000 description 4
WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
239000004088 foaming agent Substances 0.000 description 3
CUJDLRZIRYADAB-FPAZSGHZSA-N (2s)-2-acetamido-4-methylsulfanylbutanoic acid;(2s)-2-amino-5-(diaminomethylideneamino)pentanoic acid Chemical compound CSCC[C@@H](C(O)=O)NC(C)=O.OC(=O)[C@@H](N)CCCN=C(N)N CUJDLRZIRYADAB-FPAZSGHZSA-N 0.000 description 2
QZXSMBBFBXPQHI-UHFFFAOYSA-N N-(dodecanoyl)ethanolamine Chemical compound CCCCCCCCCCCC(=O)NCCO QZXSMBBFBXPQHI-UHFFFAOYSA-N 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
239000000654 additive Substances 0.000 description 2
BTBJBAZGXNKLQC-UHFFFAOYSA-N ammonium lauryl sulfate Chemical compound [NH4+].CCCCCCCCCCCCOS([O-])(=O)=O BTBJBAZGXNKLQC-UHFFFAOYSA-N 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
JLGDXLJLBLWEPD-YFKPBYRVSA-N (2r)-2-(butanoylamino)-3-sulfanylpropanoic acid Chemical compound CCCC(=O)N[C@@H](CS)C(O)=O JLGDXLJLBLWEPD-YFKPBYRVSA-N 0.000 description 1
KBBJNRLWAGIQLW-BYPYZUCNSA-N (2r)-2-(propanoylamino)-3-sulfanylpropanoic acid Chemical compound CCC(=O)N[C@@H](CS)C(O)=O KBBJNRLWAGIQLW-BYPYZUCNSA-N 0.000 description 1
CPYVQXAASIFAMD-KNIFDHDWSA-N (2s)-2-aminobutanedioic acid;(2s)-2,6-diaminohexanoic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O.NCCCC[C@H](N)C(O)=O CPYVQXAASIFAMD-KNIFDHDWSA-N 0.000 description 1
NZIOTNYOYJRBSN-UHFFFAOYSA-N 2-(butanoylamino)-4-methylsulfanylbutanoic acid Chemical compound CCCC(=O)NC(C(O)=O)CCSC NZIOTNYOYJRBSN-UHFFFAOYSA-N 0.000 description 1
208000001840 Dandruff Diseases 0.000 description 1
ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical group NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 1
KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical group NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical class CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
RBAAEQRITQHPJM-LURJTMIESA-N N-propanoyl-L-methionine Chemical compound CCC(=O)N[C@H](C(O)=O)CCSC RBAAEQRITQHPJM-LURJTMIESA-N 0.000 description 1
ZXFQDPHJZVBMJZ-UHFFFAOYSA-N OCC[N+]1(CC([O-])=O)CCN=C1 Chemical compound OCC[N+]1(CC([O-])=O)CCN=C1 ZXFQDPHJZVBMJZ-UHFFFAOYSA-N 0.000 description 1
108010009736 Protein Hydrolysates Proteins 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
229940063953 ammonium lauryl sulfate Drugs 0.000 description 1
239000002280 amphoteric surfactant Substances 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
230000003796 beauty Effects 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
238000005238 degreasing Methods 0.000 description 1
239000003599 detergent Substances 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000010696 ester oil Substances 0.000 description 1
239000004872 foam stabilizing agent Substances 0.000 description 1
210000003128 head Anatomy 0.000 description 1
HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
125000000487 histidyl group Chemical group [H]N([H])C(C(=O)O*)C([H])([H])C1=C([H])N([H])C([H])=N1 0.000 description 1
239000003906 humectant Substances 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
150000002632 lipids Chemical class 0.000 description 1
239000002932 luster Substances 0.000 description 1
229930182817 methionine Natural products 0.000 description 1
238000000034 method Methods 0.000 description 1
229940105132 myristate Drugs 0.000 description 1
SKDZEPBJPGSFHS-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)tetradecanamide Chemical compound CCCCCCCCCCCCCC(=O)N(CCO)CCO SKDZEPBJPGSFHS-UHFFFAOYSA-N 0.000 description 1
230000035515 penetration Effects 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
239000002994 raw material Substances 0.000 description 1
210000002374 sebum Anatomy 0.000 description 1
239000000344 soap Substances 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
238000005406 washing Methods 0.000 description 1

Landscapes

Cosmetics (AREA)
Detergent Compositions (AREA)

JP5903880A 1980-05-02 1980-05-02 Shampoo composition Granted JPS56155298A (en)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP5903880A JPS56155298A (en)	1980-05-02	1980-05-02	Shampoo composition

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP5903880A JPS56155298A (en)	1980-05-02	1980-05-02	Shampoo composition

Publications (2)

Publication Number	Publication Date
JPS56155298A JPS56155298A (en)	1981-12-01
JPS6129322B2 true JPS6129322B2 (no)	1986-07-05

Family

ID=13101724

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP5903880A Granted JPS56155298A (en)	1980-05-02	1980-05-02	Shampoo composition

Country Status (1)

Country	Link
JP (1)	JPS56155298A (no)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
LU84095A1 (fr) *	1982-04-19	1983-12-16	Galephar	Sels d'acetylcysteine,leur preparation et leur utilisation
JPS60218309A (ja) *	1984-04-16	1985-11-01	Nippon Oil & Fats Co Ltd	パ−ル状ヘア−リンス
SE9103572D0 (sv)	1991-11-29	1991-11-29	Astra Ab	Organic salts of n,n'-diacetyl cystine
MX9700516A (es) *	1994-07-21	1997-05-31	Minnesota Mining & Mfg	Composiciones limpiadoras concentradas capaces de incrementar su viscosidad despues de la dilucion.
FR2746316B1 (fr) *	1996-03-19	1998-06-12	Guerlain	Nouvelles compositions cosmetologiques ou dermatologiques
US6159485A (en) *	1999-01-08	2000-12-12	Yugenic Limited Partnership	N-acetyl aldosamines, n-acetylamino acids and related n-acetyl compounds and their topical use
US6808716B2 (en) *	1999-01-08	2004-10-26	Ruey J. Yu	N-acetylamino acids, related N-acetyl compounds and their topical use
JP2002047147A (ja) *	2000-07-28	2002-02-12	Hoyu Co Ltd	シャンプー組成物

Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1168591B (de) *	1958-06-28	1964-04-23	Rei Werke Ag	Hautreinigungsmittel

1980
- 1980-05-02 JP JP5903880A patent/JPS56155298A/ja active Granted

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1168591B (de) *	1958-06-28	1964-04-23	Rei Werke Ag	Hautreinigungsmittel

Also Published As

Publication number	Publication date
JPS56155298A (en)	1981-12-01

Publication	Publication Date	Title
US5710114A (en)	1998-01-20	Stable conditioning shampoo containing an anionic surfactant, a fatty alcohol, and polyethyleneimine
JPH0460084B2 (no)	1992-09-25
US4001394A (en)	1977-01-04	Shampoo creme rinse containing a quaternary ammonium saccharinate, cyclamate or phthalimidate
JPH01308218A (ja)	1989-12-12	毛染め相成物
JPS5839805B2 (ja)	1983-09-01	フケボウシザイ
EP0627216A2 (en)	1994-12-07	Stable conditioning shampoo containing an anionic surfactant, a fatty alcohol, a silicone conditioner and polyethyleneimine
JPH05201853A (ja)	1993-08-10	洗浄剤組成物
JPH0238564B2 (no)	1990-08-31
RU95103974A (ru)	1997-02-27	Моющий косметический состав глины в качестве агента для диспергирования нерастворимого кремнийорганического соединения в моющей косметической композиции
JPS60195200A (ja)	1985-10-03	洗浄剤組成物
JPS6129322B2 (no)	1986-07-05
JPH04230614A (ja)	1992-08-19	毛髪化粧料
JPH0621050B2 (ja)	1994-03-23	フケ取りシヤンプ−
US2928772A (en)	1960-03-15	Hair conditioning composition containing n (higher acyl colamino formylmethyl)pyridinium chloride and a fatty acids monoglyceride sulfate anionic detergent
JPH08510464A (ja)	1996-11-05	少なくとも１種のアルキルガラクトシドウロネート型アニオン界面活性剤および少なくとも１種のアルキルポリグリコシド型および／またはポリグリセロール型ノニオン界面活性剤を含有する化粧用組成物
HU193289B (en)	1987-09-28	Cosmetical composition for treating hair and nail containing blood plasma concentrate as active agent
JPH08333598A (ja)	1996-12-17	着色液体洗浄剤
JPH04164018A (ja)	1992-06-09	染毛剤
JP2004284964A (ja)	2004-10-14	固形洗浄剤
JPH06199654A (ja)	1994-07-19	液体身体洗浄剤組成物
KR0182599B1 (ko)	1999-05-01	모발 내부 조직을 강화하는 샴푸조성물
JPH04183797A (ja)	1992-06-30	臭気マスキング塩基性アミノ酸脂肪酸塩組成物
US3803323A (en)	1974-04-09	Isothiouronium salts for reducing the excessively oily appearance of the hair and scalp
TWI691339B (zh)	2020-04-21	洗髮劑組合物
JPS58138799A (ja)	1983-08-17	洗浄剤組成物