4-Butylbenzene-1,2-diamine

Base Information Edit

Chemical Name:4-Butylbenzene-1,2-diamine
CAS No.:3663-23-8
Molecular Formula:C10H16N2
Molecular Weight:164.25
Hs Code.:2921590090
European Community (EC) Number:222-917-7
UNII:M4GA1B83X0
DSSTox Substance ID:DTXSID3063120
Nikkaji Number:J205.577E
Wikidata:Q27283480
Mol file:3663-23-8.mol

Synonyms:4-Butylbenzene-1,2-diamine;3663-23-8;1,2-Benzenediamine, 4-butyl-;4-n-Butyl-o-phenylenediamine;o-Phenylenediamine, 4-butyl-;HSDB 6269;4-BUTYL-1,2-BENZENEDIAMINE;4-butyl-O-phenylenediamine;UNII-M4GA1B83X0;3,4-Diamino-1-butylbenzene;4-butyl-1,2-phenylenediamine;M4GA1B83X0;EINECS 222-917-7;4-n-butyl-1,2-phenylenediamine;Benzenediamine, 4-butyl-;SCHEMBL7204931;4-butyl-1,2-phenylene-diamine;DTXSID3063120;2-AMINO-4-N-BUTYLANILINE;AKOS006275172;4-BUTYL-1,2-BENZENEDIAMINE [HSDB];FT-0752998;F18184;EN300-1241624;A902678;Q27283480

Suppliers and Price of 4-Butylbenzene-1,2-diamine

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 10 raw suppliers

Chemical Property of 4-Butylbenzene-1,2-diamine Edit

Chemical Property:

Vapor Pressure:0.000998mmHg at 25°C
Refractive Index:1.584
Boiling Point:302.3 °C at 760 mmHg
Flash Point:161.7 °C
PSA：52.04000
Density:1.027 g/cm³
LogP:3.35600
XLogP3:2.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:164.131348519
Heavy Atom Count:12
Complexity:125

Purity/Quality:: 99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Nitrogen Compounds -> Amines, Aromatic
Canonical SMILES:CCCCC1=CC(=C(C=C1)N)N

Technology Process of 4-Butylbenzene-1,2-diamine

There total 9 articles about 4-Butylbenzene-1,2-diamine 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: 87.4%

: iron (III) chloride hexahydrate

: 3663-22-7
4-n-butyl-2-nitroaniline

: 3663-23-8
4-n-butyl-1,2-phenylenediamine

Guidance literature:: With hydrazine hydrate; In methanol; hexane;

Reference yield: 75.0%

: 3663-22-7
4-n-butyl-2-nitroaniline

: 3663-23-8
4-n-butyl-1,2-phenylenediamine

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; for 12h; under 760 Torr; Ambient temperature;

Reference yield:

: 104-13-2
4-Butylaniline

: 3663-23-8
4-n-butyl-1,2-phenylenediamine

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / cc. sulphuric acid / 1 h / 50 °C

2: 70 percent / fuming nitric acid, acetic anhydride / acetic acid / 6 h / -15 °C

3: 76 percent / aq. potassium hydroxide / ethanol; H₂O / 1 h / Heating

4: 75 percent / H₂ / 10percent Pd/C / methanol / 12 h / 760 Torr / Ambient temperature

With potassium hydroxide; hydrogen; nitric acid; acetic anhydride; palladium on activated charcoal; sulfuric acid; In methanol; ethanol; water; acetic acid;