4-Amino-4'-hydroxy-3-methyldiphenylamine

Base Information

• Chemical Name: 4-Amino-4'-hydroxy-3-methyldiphenylamine
• CAS No.: 6219-89-2
• Molecular Formula: C13H14 N2 O
• Molecular Weight: 214.267
• Hs Code.: 2922299090
• European Community (EC) Number: 215-483-5,228-294-8,617-726-4
• NSC Number: 37093
• UNII: 7YB07WHF8N
• DSSTox Substance ID: DTXSID9024483
• Nikkaji Number: J70.172F
• Wikidata: Q81983887
• ChEMBL ID: CHEMBL1430204
• Mol file: 6219-89-2.mol

Synonyms:Ursol Blue Grey OM;6219-89-2;4-Amino-4'-hydroxy-3-methyldiphenylamine;Kayaku Sulphur Blue RP;Thional Indone Blue RN;4-(4-Amino-3-methylanilino)phenol;Phenol, p-(4-amino-m-toluidino)-;1327-57-7;3'-Methyl-4'-amino-4-hydroxydiphenylamine;C.I. 76565;C.I. Sulphur Blue 7;4-((4-Amino-3-methylphenyl)amino)phenol;NSC 37093;CCRIS 5960;p-(4-Amino-m-toluidino)phenol;p-(4-Amino-3-toluidino)phenol;Phenol, 4-((4-amino-3-methylphenyl)amino)-;4-[(4-Amino-m-tolyl)amino]phenol;EINECS 228-294-8;4-AMINO-4'-HYDROXY-3-METHYL-DIPHENYLAMINE;BRN 3531234;7YB07WHF8N;DTXSID9024483;Phenol, 4-[(4-amino-3-methylphenyl)amino]-;4-((4-Amino-m-tolyl)amino)phenol;NSC-37093;3-13-00-01162 (Beilstein Handbook Reference);4-[(4-amino-3-methylphenyl)amino]phenol;Diresul Blue 8RS;Fenoxyl Blue L;Fenoxyl Blue LC;Sulphur Blue 7;Fenoxyl Blue 9R;Dark Blue Z;Fenoxyl Blue LCR;Diresul Blue 9RS;Immedial Indone RR;CI Sulfur Blue 7;CI Sulphur Blue 7;Eclipse Dark Blue B;Atul Sulfur Navy Blue;Mitsui Sulphur Blue R;Calcogene Blue 2B-CF;Calcogene Blue 2R-CF;Calcogene Blue 6R-CF;Diresul Navy Blue GIS;Kayaku Sulphur Blue BK;Kayaku Sulphur Blue BN;Kayaku Sulphur Blue BP;Kayaku Sulphur Blue RC;Kayaku Sulphur Blue RN;Kayaku Sulphur Blue RS;Mitsui Sulphur Blue BC;Mitsui Sulphur Blue FB;Mitsui Sulphur Blue LC;Mitsui Sulphur Blue RC;C.I. Sulfur Blue 7;Acco Sulfur Blue B-CF;Acco Sulfur Blue R-CF;Kayaku Indone Violet BC;Kayaku Sulphur Blue 4R;Mitsui Sulphur Blue 4R;Immedial Indone Violet B;Kayaku Sulphur Blue FBB;Kayaku Sulphur Blue TFB;Kayaku Sulphur Blue TFR;Mitsui Sulphur Blue LCR;Mitsui Sulphur Blue RCP;Mitsui Sulphur Blue TFA;Mitsui Sulphur Blue TFB;Mitsui Sulphur Blue 3BN;Acco Sulfur Blue 2R-CF;Acco Sulfur Blue 4R-CF;Acco Sulfur Blue 6R-CF;Acco Sulfur Blue GLP-CF;Acco Sulfur Blue GLR-CF;UNII-7YB07WHF8N;Katigen Blue BCR Conc CF;Kayaku Sulphur Indone Violet;Color Index No. 53440;Color Index Number 53440;Katigen Blue BC3R Conc CF;Katigen Blue BC8R Conc CF;Calcogene Navy Blue 2GS-CF;Colour Index No. 53440;MLS002415702;Colour Index Number 53440;DTXCID804483;SCHEMBL8092870;CHEMBL1430204;HSDB 5811;NSC37093;EINECS 215-483-5;Tox21_200344;AKOS022506291;4-(4-Amino-3-methylanilino)phenol #;LS-1490;NCGC00091825-01;NCGC00091825-02;NCGC00091825-03;NCGC00257898-01;CI 53440;SMR001370890;CAS-6219-89-2;4-(4-AMINO-META-TOLUIDINO)-PHENOL;C.I.76565;C.I. 53440;AMINO-4'-HYDROXY-3-METHYLDIPHENYLAMINE, 4-

Chemical Property of 4-Amino-4'-hydroxy-3-methyldiphenylamine

Chemical Property:

• Vapor Pressure: 1.39E-06mmHg at 25°C
• Refractive Index: 1.6450 (estimate)
• Boiling Point: 388.2°C at 760 mmHg
• Flash Point: 188.6°C
• PSA: 58.28000
• Density: 1.242g/cm³
• LogP: 3.68060
• XLogP3: 2.4
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 214.110613074
• Heavy Atom Count: 16
• Complexity: 214

Purity/Quality:

99.0% Min. ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Dyes -> Other Dyes
• Canonical SMILES: CC1=C(C=CC(=C1)NC2=CC=C(C=C2)O)N

Technology Process of 4-Amino-4'-hydroxy-3-methyldiphenylamine

There total 2 articles about 4-Amino-4'-hydroxy-3-methyldiphenylamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ 4-(4-Amino-3-methyl-anilino)-phenol (6219-89-2)

Guidance literature:

With hydrogen sulfide;

Reference yield:

4-amino-phenol (123-30-8) + o-toluidine (95-53-4) → 4-(4-Amino-3-methyl-anilino)-phenol (6219-89-2)

Guidance literature:

in saurer Loesung und reduziert man das so entstandene Indophenol mit Schwefelnatrium;

upstream raw materials:

4-amino-phenol

o-toluidine