2,5-Diaminobenzyl alcohol

Base Information

• Chemical Name: 2,5-Diaminobenzyl alcohol
• CAS No.: 73793-80-3
• Molecular Formula: C7H10 N2 O
• Molecular Weight: 138.169
• European Community (EC) Number: 277-611-6
• DSSTox Substance ID: DTXSID40994772
• Nikkaji Number: J291.278C
• Wikidata: Q82985820
• Mol file: 73793-80-3.mol

Synonyms:2,5-Diaminobenzyl alcohol;(2,5-diaminophenyl)methanol;73793-80-3;EINECS 277-611-6;Benzenemethanol, 2,5-diamino-;2,5-Diaminobenzenemethanol;SCHEMBL33604;DTXSID40994772;2-hydroxymethyl-p-phenylenediamine;NKNCGBHPGCHYCQ-UHFFFAOYSA-N;AKOS006340639

Chemical Property of 2,5-Diaminobenzyl alcohol

Chemical Property:

• Vapor Pressure: 4.6E-06mmHg at 25°C
• Boiling Point: 368°Cat760mmHg
• Flash Point: 176.4°C
• PSA: 72.27000
• Density: 1.281g/cm³
• LogP: 1.50570
• XLogP3: 0.2
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 138.079312947
• Heavy Atom Count: 10
• Complexity: 108

Purity/Quality:

98%Min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C=C1N)CO)N

Technology Process of 2,5-Diaminobenzyl alcohol

There total 8 articles about 2,5-Diaminobenzyl alcohol 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:

2-(hydroxymethyl)-4-{(E)-[2-(hydroxymethyl)phenyl]diazenyl}aniline → 2-Aminobenzyl alcohol (5344-90-1) + 2-hydroxymethyl-1,4-diaminobenzene (73793-80-3)

Guidance literature:

With palladium 10% on activated carbon; hydrogen; In water; ethyl acetate; at 20 - 40 ℃; under 1500.15 - 2250.23 Torr;

Reference yield:

(5-amino-2-nitro-phenyl)-methanol (77376-03-5) → 2-hydroxymethyl-1,4-diaminobenzene (73793-80-3)

Guidance literature:

With nickel; Hydrogenation;

Reference yield:

(2-amino-5-nitrophenyl)methanol (77242-30-9) → 2-hydroxymethyl-1,4-diaminobenzene (73793-80-3)

Guidance literature:

With calcium chloride; zinc;

upstream raw materials:

(2-amino-5-nitrophenyl)methanol

(5-amino-2-nitro-phenyl)-methanol

2-Aminobenzyl alcohol

N-(3-formylphenyl)acetamide

Downstream raw materials:

2-(methoxymethyl)-p-phenylenediamine

Refernces

• 1、 -. "1,3-Dihydroxybenzene derivatives and colorants containing said compounds". . . Retrieved 2008/06/13.
• 2、 -. "Methods for dyeing keratinous fibers with compositions which contain aminoindole couplers, oxidation dye precursors, and oxidizing agents at acid pHs". . . Retrieved 2008/06/13.