11596
2,2′-Azobis(2-methylbutyronitrile)
≥98.0%
Synonym(s):
2,2′-(1,2-Diazenediyl)bis[2-methylbutanenitrile], 2,2′-(Diazene-1,2-diyl)bis(2-methylbutanenitrile), 2,2′-Azobis(2-cyanobutane), 2,2′-Dimethyl-2,2′-azodibutyronitrile, 2-[2-(1-Cyano-1-methylpropyl)diazen-1-yl]-2-methylbutanenitrile, Azobisisoamylonitrile, Azocatalyst M
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About This Item
Empirical Formula (Hill Notation):
C10H16N4
CAS Number:
Molecular Weight:
192.26
UNSPSC Code:
12352102
NACRES:
NA.22
PubChem Substance ID:
EC Number:
236-740-8
Beilstein/REAXYS Number:
1710306
MDL number:
Assay:
≥98.0%
Form:
solid
Quality Segment
assay
≥98.0%
form
solid
mp
49-52 °C
functional group
azo, nitrile
storage temp.
2-8°C
SMILES string
CCC(C)(\N=N\C(C)(CC)C#N)C#N
InChI
1S/C10H16N4/c1-5-9(3,7-11)13-14-10(4,6-2)8-12/h5-6H2,1-4H3/b14-13+
InChI key
AVTLBBWTUPQRAY-BUHFOSPRSA-N
General description
2,2′-Azobis(2-methylbutyronitrile), also known as AMBN, is a free radical initiator that is widely used in organic synthesis for a variety of reactions. It is often used as an initiator in the synthesis of various polymers, such as polystyrene, polyacrylamide, and poly(methyl methacrylate).
Application
2,2′-Azobis(2-methylbutyronitrile) can be used as a radical initiator in the synthesis of bibenzo[b][1,4]thiazine derivatives by a free-radical condensation reaction 2,2′-dithiodianiline and methyl aryl ketones. It is also used in the synthesis of polyacrylonitrile nanoparticles via semi-continuous emulsion polymerization.
Preparation Note
Warning: these products are subject to the Explosives Act and must be transported refrigerated - additional costs for transport will apply.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Self-react. D
Storage Class
4.1A - Other explosive hazardous materials
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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