21371-44-8

Basic information

• Product Name: Benzenamine, 3,3'-azobis-
• CAS NO: 21371-44-8
• Molecular Formula: C12H12N4
• Molecular Weight: 212.254
• Mol File: 21371-44-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenamine, 3,3'-azobis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 3,3'-azobis-(21371-44-8)
• EPA Substance Registry System: Benzenamine, 3,3'-azobis-(21371-44-8)

Safety Data

• Hazardous Substances Data: 21371-44-8(Hazardous Substances Data)

Upstream product

• 108-45-2 m-phenylenediamine 
• 98-95-3 nitrobenzene 
• 99-09-2 3-nitro-aniline 
• 95766-63-5 N,N'-bis-(3-amino-phenyl)-hydrazine 
• 7664-93-9 sulfuric acid 
• 64-17-5 ethanol 
• 6283-26-7 2-hydroxy-5-(3-nitro-phenylazo)-benzoic acid 
• 69-72-7 salicylic acid 
• 16278-29-8 3-nitrobenzenediazonium 
• 99-65-0 meta-dinitrobenzene 
• 111-42-2 2,2'-iminobis[ethanol] 
• 102-71-6 triethanolamine 
• 101-13-3 3,3'-diaminoazoxybenzene 

Downstream Products

• 859951-92-1 N¹-[3-(3-amino-phenylazo)-phenyl]-4-nitro-o-phenylenediamine 
• 132466-20-7 bis-(3-acetoxy-phenyl)-diazene 
• 70894-13-2 4,4'-diamino-[1,1'-biphenyl] -2,2'-diol 
• 140661-76-3 3,3'-Bisazobenzol 
• 140676-46-6 7,22-Bis(4-methoxyphenylsulfonyl)-7,14,15,22-tetraaza<7.2.7.1>(1,3)(1,3)(1,4)(1,4)cyclophan-14-en 
• 140676-45-5 6,21-Bis(4-methoxyphenylsulfonyl)-6,13,14,21-tetraaza<6.2.6.1>(1,3)(1,3)(1,4)(1,4)cyclophan-13-en 
• 140661-55-8 5,20-Bis(4-methoxyphenylsulfonyl)-5,12,13,20-tetraaza<5.2.5.1>(1,3)(1,3)(1,4)(1,4)cyclophan-12-en 
• 140661-54-7 4,19-Bis(4-methoxyphenylsulfonyl)-4,11,12,19-tetraaza<4.2.4.1>(1,3)(1,3)(1,4)(1,4)cyclophan-11-en 
• 140661-73-0 3,3'-Bis<(4-methoxyphenylsulfonyl)octylamino>azobenzol 
• 140661-75-2 3,3'-Bisazobenzol 
• 140661-74-1 3,3'-Bis(octylamino)azobenzol 
• 140661-45-6 13,37-Bis(methoxycarbonyl)-9,18,33,42-tetrakis(4-methoxyphenylsulfonyl)-1,2,9,18,25,26,33,42-octaaza<2.2.2.2.2.2>(1,3)cyclophan-1,25-dien 
• 140661-33-2 3,3'-Bis<(4-methoxyphenylsulfonyl)amino>azobenzol 
• 55631-07-7 bis-(3-phenylazo-phenyl)-diazene 

Relevant articles and documents

Reduction of Aromatic Nitro Compounds by Ethylenediamine. A New Selective Reagent for the Synthesis of Symmetric Azo Compounds

Ethylenediamine selectively reduces aromatic nitro compounds RC6H4NO2 (R = H, m-CH3, p-CH3, and m-Ph) at 150 deg C to symmetric azo compounds RC6H4N=NC6H4R in good yield but does not reduce their ortho-substituted analogues.The diamine does not react with o- or p-nitroanilines but reduces the meta isomer to 1,3-diaminobenzene and 3,3'-diaminoazobenzene.Its reaction with o- and p-halonitrobenzenes gives substitution products H2NCH2CH2NHC6H4NO2.Nitrosobenzene is reduced to aniline and azobenzene, while α-nitroso-β-naphthol is converted to 1,4-phenanthroline.Among a variety of other amines tested, only 1,3-propylenediamine reduces nitrobenzene to azobenzene.A mechanism for the reaction is proposed.

Evaporator system comprising a stabilized pesticidal phosphoric acid ester and method for stabilizing such ester enclosed in an evaporator

An evaporator system adapted for emitting insect killing vapors of an insecticide therefrom and comprising a liquid or solid composition enclosed therein, said insecticide consisting in at least one volatile phosphoric acid ester which is stabilized by at least one diazene compound.