4-Aminoazobenzene hydrochloride

Base Information

• Chemical Name: 4-Aminoazobenzene hydrochloride
• CAS No.: 3457-98-5
• Molecular Formula: C12H11 N3 . Cl H
• Molecular Weight: 233.7
• Hs Code.: 29215900
• European Community (EC) Number: 222-390-3
• DSSTox Substance ID: DTXSID40883975
• Wikidata: Q26840889
• Mol file: 3457-98-5.mol

Synonyms:3457-98-5;4-Aminoazobenzene hydrochloride;4-(Phenyldiazenyl)aniline hydrochloride;287481-35-0;4-Aminobenzene Hydrochloride;Benzenamine, 4-(phenylazo)-, monohydrochloride;4-phenyldiazenylaniline;hydrochloride;(E)-4-Aminoazobenzene hydrochloride;p-Aminoazobenzene hydrochloride;(E)-4-(phenyldiazenyl)aniline hydrochloride;4-[(1E)-2-phenyldiazen-1-yl]aniline hydrochloride;p-Aminoazobenzene HCl;4-(Phenylazo)aniline Hydrochloride;p-Aminoazobenzolhydrochlorid;4-phenylazoaniline;SCHEMBL2382817;DTXSID40883975;MFCD00012994;4-(Phenyldiazenyl)anilinehydrochloride;AKOS015913151;AKOS028109572;P-AMINODIPHENYLIMIDE HYDROCHLORIDE;AS-64031;A0771;CS-0320548;FT-0689107;W-106726;Q26840889

Chemical Property of 4-Aminoazobenzene hydrochloride

Chemical Property:

• Vapor Pressure: 2.19E-05mmHg at 25°C
• Melting Point: 213 °C
• Boiling Point: 360.7°Cat760mmHg
• Flash Point: 171.9°C
• PSA: 50.74000
• Density: g/cm³
• LogP: 5.06740
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 233.0719751
• Heavy Atom Count: 16
• Complexity: 201

Purity/Quality:

99% ^*data from raw suppliers

4-Aminoazobenzene Hydrochloride >98.0%(T) ^*data from reagent suppliers

Safty Information:

• Hazard Codes: T
• Statements: 45-46-20/21/22-36/37/38
• Safety Statements: 53-22-26-36/37/39-45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)N=NC2=CC=C(C=C2)N.Cl

Technology Process of 4-Aminoazobenzene hydrochloride

There total 2 articles about 4-Aminoazobenzene hydrochloride 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:

aniline yellow (60-09-3) → 4-(phenyldiazenyl)aniline hydrochloride (3457-98-5)

Guidance literature:

With diethyl ether; acetyl chloride;

Reference yield:

4-phenylazoaniline hydrochloride (3457-98-5) → 4-(phenyldiazenyl)aniline hydrochloride (3457-98-5)

Guidance literature:

With water; sodium chloride;

Reference yield: 84.0%

methyl 8-chloro-8-oxooctanoate (41624-92-4) + 4-(phenyldiazenyl)aniline hydrochloride (3457-98-5) → methyl 8-oxo-8-((4-(phenyldiazenyl)phenyl)amino)octanoate

Guidance literature:

With triethylamine; In dichloromethane; at 0 ℃; for 1h;

upstream raw materials:

aniline yellow

Downstream raw materials:

4-cyanoazobenzene

N-sulfinyl-p-(phenylazo)aniline

4-aminoazobenzene-3,4'-disulfonic acid

4'-aminoazobenzene-4-sulfonic acid