1808-39-5

Upstream product

• 53313-86-3 Bis-(isobutyronitril-2-azo-3'-isovaleroyl)-peroxid 

Downstream Products

• 62830-53-9 NSC 26654 
• 1260370-23-7 1-(2-methylpropyl)-4-phenyl-1,2,3-triazole 
• 1315275-25-2 N-(4-methyl-1-phenylpentyl)acetamide 
• 75437-07-9 [(1E)-4-methyl-1-penten-1-yl]benzene 
• 54624-34-9 [(1Z)-4-methyl-1-penten-1-yl]benzene 
• 4630-45-9 isobutyl radical 
• 592-13-2 2,5-dimethylhexane 
• 115-11-7 isobutene 

Relevant academic research and scientific papers

Azoperoxides. VI. Selective Decomposition of β-Azoacylperoxides

The selective decomposition of the O-O-groups in the azoperoxides 1 and 2 is possible by reaction with dimethylaniline at 35 deg C.Rate constants were measured and the decomposition products were analyzed.Intermediates are azoalkyl radicals.The radical yield of the amine induced decomposition of 2 in ethylbenzene is 8.2percent at 35 deg C.UV irradiation of the azoperoxides 1 and 2 at 20 deg C in ethylbenzene results in a quantitative and selective decomposition of the azo groups.Intermediates are C-radicals with intact peroxide groups.The reaction of 1 and 2 with triethylstannane yields reduction products of the O-O-groups and the N=N-groups, respectively.