CA2024509A1 - Procede de teinture et de permanentage des cheveux - Google Patents

Procede de teinture et de permanentage des cheveux

Info

Publication number: CA2024509A1
Authority: CA; Canada
Prior art keywords: hair; reducing agent; composition; dye; isothiuronium
Prior art date: 1990-08-03
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.): Abandoned

Application number

CA002024509A

Other languages

English (en)

Inventor

Bryan P. Murphy

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.)

Bristol Myers Squibb Co

Original Assignee

Bristol Myers Squibb Co

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.)

1990-08-03

Filing date

1990-09-10

Publication date

1992-02-04

1990-09-10 Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co

1992-02-04 Publication of CA2024509A1 publication Critical patent/CA2024509A1/fr

Status Abandoned legal-status Critical Current

Links

238000000034 method Methods 0.000 title claims description 11
230000008569 process Effects 0.000 title claims description 10
238000004043 dyeing Methods 0.000 title abstract description 14
210000004209 hair Anatomy 0.000 claims abstract description 50
INDZTCRIYSRWOH-UHFFFAOYSA-N undec-10-enyl carbamimidothioate;hydroiodide Chemical compound I.NC(=N)SCCCCCCCCCC=C INDZTCRIYSRWOH-UHFFFAOYSA-N 0.000 claims abstract description 8
239000000203 mixture Substances 0.000 claims description 28
239000003638 chemical reducing agent Substances 0.000 claims description 25
239000007800 oxidant agent Substances 0.000 claims description 15
230000001590 oxidative effect Effects 0.000 claims description 11
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical group NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 11
238000004040 coloring Methods 0.000 claims description 10
150000002978 peroxides Chemical class 0.000 claims description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
CWERGRDVMFNCDR-UHFFFAOYSA-M thioglycolate(1-) Chemical compound [O-]C(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-M 0.000 claims description 4
CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical group OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 claims description 4
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
125000006501 nitrophenyl group Chemical group 0.000 claims description 3
229910052700 potassium Inorganic materials 0.000 claims description 3
239000011591 potassium Substances 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 claims 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group 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 claims 2
229910052708 sodium Inorganic materials 0.000 claims 2
239000011734 sodium Substances 0.000 claims 2
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 2
239000003086 colorant Substances 0.000 abstract description 11
239000000975 dye Substances 0.000 description 28
230000003647 oxidation Effects 0.000 description 12
238000007254 oxidation reaction Methods 0.000 description 12
239000003795 chemical substances by application Substances 0.000 description 9
150000001875 compounds Chemical class 0.000 description 7
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 5
239000002453 shampoo Substances 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 4
-1 isothiuronium salt Chemical class 0.000 description 4
230000002040 relaxant effect Effects 0.000 description 4
125000001424 substituent group Chemical group 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
ZZTCCAPMZLDHFM-UHFFFAOYSA-N ammonium thioglycolate Chemical compound [NH4+].[O-]C(=O)CS ZZTCCAPMZLDHFM-UHFFFAOYSA-N 0.000 description 3
239000003153 chemical reaction reagent Substances 0.000 description 3
230000009467 reduction Effects 0.000 description 3
239000000758 substrate Substances 0.000 description 3
239000008399 tap water Substances 0.000 description 3
235000020679 tap water Nutrition 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
239000000835 fiber Substances 0.000 description 2
239000006260 foam Substances 0.000 description 2
239000000499 gel Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
238000002407 reforming Methods 0.000 description 2
150000003573 thiols Chemical class 0.000 description 2
WAXMTENYNOYEBU-UHFFFAOYSA-N 1-phenylanthracene-9,10-dione Chemical class O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2C1=CC=CC=C1 WAXMTENYNOYEBU-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
230000009471 action Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000005456 alcohol based solvent Substances 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
239000004599 antimicrobial Substances 0.000 description 1
238000013459 approach Methods 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
125000006267 biphenyl group Chemical group 0.000 description 1
238000000861 blow drying Methods 0.000 description 1
SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Chemical class [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 1
230000001680 brushing effect Effects 0.000 description 1
239000000872 buffer Substances 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
230000008859 change Effects 0.000 description 1
230000003750 conditioning effect Effects 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000006184 cosolvent Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
210000004919 hair shaft Anatomy 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
210000003128 head Anatomy 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002791 naphthoquinones Chemical group 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
239000003002 pH adjusting agent Substances 0.000 description 1
239000006072 paste Substances 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
238000002203 pretreatment Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
210000004761 scalp Anatomy 0.000 description 1
GNBVPFITFYNRCN-UHFFFAOYSA-M sodium thioglycolate Chemical compound [Na+].[O-]C(=O)CS GNBVPFITFYNRCN-UHFFFAOYSA-M 0.000 description 1
238000005507 spraying Methods 0.000 description 1
230000007480 spreading Effects 0.000 description 1
230000000153 supplemental effect Effects 0.000 description 1
230000009974 thixotropic effect Effects 0.000 description 1
125000005425 toluyl group Chemical group 0.000 description 1
210000002268 wool Anatomy 0.000 description 1

Landscapes

Cosmetics (AREA)

CA002024509A 1990-08-03 1990-09-10 Procede de teinture et de permanentage des cheveux Abandoned CA2024509A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US56253090A	1990-08-03	1990-08-03
US562,530		1990-08-03

Publications (1)

Publication Number	Publication Date
CA2024509A1 true CA2024509A1 (fr)	1992-02-04

Family

ID=24246654

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA002024509A Abandoned CA2024509A1 (fr)	1990-08-03	1990-09-10	Procede de teinture et de permanentage des cheveux

Country Status (1)

Country	Link
CA (1)	CA2024509A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6989149B2 (en)	2001-01-17	2006-01-24	Glenn Jr Robert Wayne	Delivery of reactive agents via self emulsification for use in shelf-stable products
WO2007110535A2 (fr)	2006-03-24	2007-10-04	L'oréal	Composition de teinture comprenant un colorant fluorescent thiol/disulfure a groupe ortho-pyridinium a chaine alkylene interrompue et a charge cationique interne, procede d'eclaircissement des matieres keratiniques a partir de ce colorant

1990
- 1990-09-10 CA CA002024509A patent/CA2024509A1/fr not_active Abandoned

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6989149B2 (en)	2001-01-17	2006-01-24	Glenn Jr Robert Wayne	Delivery of reactive agents via self emulsification for use in shelf-stable products
WO2007110535A2 (fr)	2006-03-24	2007-10-04	L'oréal	Composition de teinture comprenant un colorant fluorescent thiol/disulfure a groupe ortho-pyridinium a chaine alkylene interrompue et a charge cationique interne, procede d'eclaircissement des matieres keratiniques a partir de ce colorant

Legal Events

Date	Code	Title	Description
1995-03-11	FZDE	Dead

Publication	Publication Date	Title
US4804385A (en)	1989-02-14	Process for dyeing keratinous fibres with 5,6-dihydroxy-indole combined with an iodide and dyeing composition employed
US4840639A (en)	1989-06-20	Agent for dyeing hair
KR100242359B1 (ko)	2000-03-02	특정한 직접 염료를 함유하는 케라틴 섬유의 연조 염료 조성물
US5019130A (en)	1991-05-28	Substituted N-aryl pyrroles in oxidative hair dye compositions
RU2185142C2 (ru)	2002-07-20	Композиция для окраски кератиновых волокон, способы их окраски, упаковка набора для окраски кератиновых волокон
JPH0460580B2 (fr)	1992-09-28
JPH08501322A (ja)	1996-02-13	ケラチン含有繊維を染色するための方法
US5011500A (en)	1991-04-30	Process for dyeing keratinous fibres and dye composition employing indole derivatives and direct nitro dyes
PL204979B1 (pl)	2010-02-26	Kompozycja do farbowania włókien keratynowych, sposób farbowania oraz zestaw do farbowania z wykorzystaniem tej kompozycji
JP2008044959A (ja)	2008-02-28	カチオン性直接着色剤と第４級アンモニウム塩を含有するケラチン繊維の染色用組成物
HU222990B1 (hu)	2004-01-28	Kétlépéses eljárás keratintartalmú rostok direkt festésére bázisos direkt színezékek alkalmazásával
JPH07501062A (ja)	1995-02-02	染毛製剤用の添加剤としての５，６−ジヒドロキシインドリン
US4395262A (en)	1983-07-26	Hair dyeing agent
RU2179843C2 (ru)	2002-02-27	Композиция для крашения кератиновых волокон, способ их крашения, набор для крашения кератиновых волокон
JPS58105909A (ja)	1983-06-24	染毛料
JPH01149708A (ja)	1989-06-12	毛髪処理用組成物
CA2024509A1 (fr)	1992-02-04	Procede de teinture et de permanentage des cheveux
JP3686352B2 (ja)	2005-08-24	毛髪脱色剤
JPH01501003A (ja)	1989-04-06	毛髪の色を永久的に変えるのに使用する組成物
JP3577841B2 (ja)	2004-10-20	毛髪処理剤組成物
JPH09278636A (ja)	1997-10-28	毛髪用染色剤
JPH06145032A (ja)	1994-05-24	粉末状染毛剤
US4832697A (en)	1989-05-23	Hair dye preparations containing substantive nitrodiphenylamine derivatives
JP3572807B2 (ja)	2004-10-06	毛髪処理剤組成物
JPH09278637A (ja)	1997-10-28	酸化毛髪染色剤

CA2024509A1 - Procede de teinture et de permanentage des cheveux - Google Patents

Info

Links

Landscapes

Applications Claiming Priority (2)

Publications (1)

Family

ID=24246654

Family Applications (1)

Country Status (1)

Cited By (2)

Cited By (2)

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Legal Events