GB954253A - N:n - disubstituted - nitro - phenylene - diamines and their use in hair dyeing compositions - Google Patents
N:n - disubstituted - nitro - phenylene - diamines and their use in hair dyeing compositionsInfo
- Publication number
- GB954253A GB954253A GB3599561A GB3599561A GB954253A GB 954253 A GB954253 A GB 954253A GB 3599561 A GB3599561 A GB 3599561A GB 3599561 A GB3599561 A GB 3599561A GB 954253 A GB954253 A GB 954253A
- Authority
- GB
- United Kingdom
- Prior art keywords
- nitro
- aminobenzene
- methylamino
- hydroxyethyl
- amino
- 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
- 239000000203 mixture Substances 0.000 title abstract 8
- 238000004043 dyeing Methods 0.000 title abstract 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 12
- 125000004432 carbon atom Chemical group C* 0.000 abstract 12
- 150000001875 compounds Chemical class 0.000 abstract 8
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 8
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 6
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 abstract 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- HVHNMNGARPCGGD-UHFFFAOYSA-N 2-nitro-p-phenylenediamine Chemical group NC1=CC=C(N)C([N+]([O-])=O)=C1 HVHNMNGARPCGGD-UHFFFAOYSA-N 0.000 abstract 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract 4
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 abstract 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- -1 alkylene chlorhydrin Chemical compound 0.000 abstract 3
- 125000003827 glycol group Chemical group 0.000 abstract 3
- 229920001515 polyalkylene glycol Chemical group 0.000 abstract 3
- MYOOTZAUHFEBBL-UHFFFAOYSA-N 1-n,4-n-dimethyl-2-nitrobenzene-1,4-diamine Chemical compound CNC1=CC=C(NC)C([N+]([O-])=O)=C1 MYOOTZAUHFEBBL-UHFFFAOYSA-N 0.000 abstract 2
- SSZWWUDQMAHNAQ-UHFFFAOYSA-N 3-chloropropane-1,2-diol Chemical compound OCC(O)CCl SSZWWUDQMAHNAQ-UHFFFAOYSA-N 0.000 abstract 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 abstract 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 2
- 244000172533 Viola sororia Species 0.000 abstract 2
- 229940100198 alkylating agent Drugs 0.000 abstract 2
- 239000002168 alkylating agent Substances 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 238000009903 catalytic hydrogenation reaction Methods 0.000 abstract 2
- 239000000975 dye Substances 0.000 abstract 2
- 230000007062 hydrolysis Effects 0.000 abstract 2
- 238000006460 hydrolysis reaction Methods 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 2
- 239000000243 solution Substances 0.000 abstract 2
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 2
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 abstract 2
- CUUOESLUUQBFTM-UHFFFAOYSA-N 1-n-methyl-2-nitrobenzene-1,4-diamine Chemical compound CNC1=CC=C(N)C=C1[N+]([O-])=O CUUOESLUUQBFTM-UHFFFAOYSA-N 0.000 abstract 1
- WHJNKCNHEVCICH-UHFFFAOYSA-N 2-nitro-1-n-phenylbenzene-1,4-diamine Chemical compound [O-][N+](=O)C1=CC(N)=CC=C1NC1=CC=CC=C1 WHJNKCNHEVCICH-UHFFFAOYSA-N 0.000 abstract 1
- UOFSMFMNGAKHJO-UHFFFAOYSA-N 4-methyl-3-nitrobenzene-1,2-diamine Chemical compound CC1=CC=C(N)C(N)=C1[N+]([O-])=O UOFSMFMNGAKHJO-UHFFFAOYSA-N 0.000 abstract 1
- ODAHDXUNSYCNRO-UHFFFAOYSA-N 4-methyl-N-[4-(methylamino)-3-nitrophenyl]benzenesulfonamide Chemical compound CNC1=C(C=C(C=C1)NS(=O)(=O)C1=CC=C(C)C=C1)[N+](=O)[O-] ODAHDXUNSYCNRO-UHFFFAOYSA-N 0.000 abstract 1
- XSHZMHVULBOPDY-UHFFFAOYSA-N 4-n-methyl-2-nitrobenzene-1,4-diamine Chemical compound CNC1=CC=C(N)C([N+]([O-])=O)=C1 XSHZMHVULBOPDY-UHFFFAOYSA-N 0.000 abstract 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 abstract 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 abstract 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 abstract 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 abstract 1
- 229920002125 Sokalan® Polymers 0.000 abstract 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 abstract 1
- 235000005811 Viola adunca Nutrition 0.000 abstract 1
- 240000009038 Viola odorata Species 0.000 abstract 1
- 235000013487 Viola odorata Nutrition 0.000 abstract 1
- 235000002254 Viola papilionacea Nutrition 0.000 abstract 1
- 239000012670 alkaline solution Substances 0.000 abstract 1
- 239000000908 ammonium hydroxide Substances 0.000 abstract 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 239000012736 aqueous medium Substances 0.000 abstract 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 abstract 1
- 239000011575 calcium Substances 0.000 abstract 1
- 229910052791 calcium Inorganic materials 0.000 abstract 1
- 235000011116 calcium hydroxide Nutrition 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000003086 colorant Substances 0.000 abstract 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 abstract 1
- 239000002270 dispersing agent Substances 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 abstract 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 239000000499 gel Substances 0.000 abstract 1
- 238000005984 hydrogenation reaction Methods 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical class [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 abstract 1
- 235000012254 magnesium hydroxide Nutrition 0.000 abstract 1
- IQEJEZOCXWJNKR-UHFFFAOYSA-N n-methyl-2,4-dinitroaniline Chemical compound CNC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O IQEJEZOCXWJNKR-UHFFFAOYSA-N 0.000 abstract 1
- 239000001005 nitro dye Substances 0.000 abstract 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 1
- 239000004584 polyacrylic acid Substances 0.000 abstract 1
- 235000011118 potassium hydroxide Nutrition 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 abstract 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 1
- 229910000029 sodium carbonate Inorganic materials 0.000 abstract 1
- 235000011121 sodium hydroxide Nutrition 0.000 abstract 1
- URLJMZWTXZTZRR-UHFFFAOYSA-N sodium myristyl sulfate Chemical compound CCCCCCCCCCCCCCOS(O)(=O)=O URLJMZWTXZTZRR-UHFFFAOYSA-N 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 229960004418 trolamine Drugs 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/418—Amines containing nitro groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US6716660A | 1960-11-04 | 1960-11-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB954253A true GB954253A (en) | 1964-04-02 |
Family
ID=22074146
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3599561A Expired GB954253A (en) | 1960-11-04 | 1961-10-06 | N:n - disubstituted - nitro - phenylene - diamines and their use in hair dyeing compositions |
Country Status (3)
| Country | Link |
|---|---|
| CH (1) | CH450633A (enrdf_load_stackoverflow) |
| DE (1) | DE1299002C2 (enrdf_load_stackoverflow) |
| GB (1) | GB954253A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1569807A1 (de) * | 1964-11-19 | 1970-07-09 | Oreal | Haarfaerbemittel |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3442861A1 (de) * | 1984-11-24 | 1986-05-28 | Wella Ag, 6100 Darmstadt | 4-(n-ethyl, n-2'-hydroxyethyl)-amino-1-(2"-hydroxyethyl)-amino-2-nitro-benzol und mittel zur faerbung von haaren |
| DE4240684A1 (de) * | 1992-12-03 | 1994-06-09 | Henkel Kgaa | Allylamino-nitroaromaten |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE928909C (de) * | 1951-02-07 | 1955-06-13 | Kleinol Produktion G M B H | Verfahren zum Faerben von tierischen Fasern, insbesondere von menschlichen Haaren, ohne Zuhilfenahme von Oxydationsmitteln |
| DE1017750B (de) * | 1954-05-31 | 1957-10-17 | Kleinol Produktion G M B H | Verfahren und Mittel zum Faerben von tierischen Fasern, insbesondere von menschlichem Haar |
-
1961
- 1961-10-06 GB GB3599561A patent/GB954253A/en not_active Expired
- 1961-10-30 DE DE1961B0064591 patent/DE1299002C2/de not_active Expired
- 1961-11-03 CH CH1276461A patent/CH450633A/de unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1569807A1 (de) * | 1964-11-19 | 1970-07-09 | Oreal | Haarfaerbemittel |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1299002B (enrdf_load_stackoverflow) | 1969-07-10 |
| CH450633A (de) | 1968-01-31 |
| DE1299002C2 (de) | 1980-05-08 |
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