C.I. Basic Violet 14, carbinol

Base Information

• Chemical Name: C.I. Basic Violet 14, carbinol
• CAS No.: 76-82-4
• Molecular Formula: C20H21 N3 O
• Molecular Weight: 319.406
• DSSTox Substance ID: DTXSID90226898
• Wikidata: Q83106472
• Mol file: 76-82-4.mol

Synonyms:C.I. Basic Violet 14, carbinol;76-82-4;Triamino-diphenyl-tolylcarbinol;Methanol, bis(p-aminophenyl)(4-amino-m-tolyl)-;C20H21N3O;4-Amino-alpha,alpha-bis(4-aminophenyl)-3-methylbenzenemethanol;Benzenemethanol, 4-amino-alpha,alpha-bis(4-aminophenyl)-3-methyl-;SCHEMBL3355114;DTXSID90226898;Benzenemethanol, 4-amino-.alpha.,.alpha.-bis(4-aminophenyl)-3-methyl-

Chemical Property of C.I. Basic Violet 14, carbinol

Chemical Property:

• Vapor Pressure: 3.92E-15mmHg at 25°C
• Boiling Point: 597.7°C at 760 mmHg
• Flash Point: 315.3°C
• PSA: 98.29000
• Density: 1.26g/cm³
• LogP: 4.76940
• XLogP3: 2.2
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 319.168462302
• Heavy Atom Count: 24
• Complexity: 378

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(C=CC(=C1)C(C2=CC=C(C=C2)N)(C3=CC=C(C=C3)N)O)N

Technology Process of C.I. Basic Violet 14, carbinol

There total 20 articles about C.I. Basic Violet 14, carbinol 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:

p-toluidine (106-49-0,12221-03-3) + aniline (62-53-3) + o-toluidine (95-53-4) → pararosaniline (467-62-9) + (4-Amino-3-methyl-phenyl)-bis-(4-amino-phenyl)-methanol (76-82-4)

Guidance literature:

entsteht in Form von Farbsalzen;

Reference yield:

p-toluidine (106-49-0,12221-03-3) + aniline (62-53-3) + o-toluidine (95-53-4) → (4-Amino-3-methyl-phenyl)-bis-(4-amino-phenyl)-methanol (76-82-4) + diphenylamine (122-39-4)

Guidance literature:

entsteht in Form von Farbsalzen;

Reference yield:

aniline hydrochloride (142-04-1,36663-09-9) + aniline (62-53-3) + 2,4-Xylidine (95-68-1) → (4-Amino-3-methyl-phenyl)-bis-(4-amino-phenyl)-methanol (76-82-4)

Guidance literature:

With nitrobenzene; iron(II) chloride; at 185 ℃; das Chlorid entsteht;

DOI:10.1021/ja01308a029

upstream raw materials:

(4-amino-3-methyl-phenyl)-bis-(4-amino-phenyl)-methane

Fuchsin

p-toluidine

aniline

Downstream raw materials:

(4-amino-3-methyl-phenyl)-bis-(4-amino-phenyl)-acetonitrile

4,4'-Dihydroxybenzophenone

4-(4,4'-dihydroxy-3-methyl-benzhydrylidene)-cyclohexa-2,5-dienone

4,4'-diamino-3-methyl-benzophenone