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11596

Sigma-Aldrich

2,2′-Azobis(2-methylbutyronitrile)

≥98.0%

Sinônimo(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

Fórmula empírica (Notação de Hill):
C10H16N4
Número CAS:
Peso molecular:
192.26
Beilstein:
1710306
Número CE:
Número MDL:
Código UNSPSC:
12352102
ID de substância PubChem:
NACRES:
NA.22

Nível de qualidade

Ensaio

≥98.0%

Formulário

solid

pf

49-52 °C

grupo funcional

azo
nitrile

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

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+

chave InChI

AVTLBBWTUPQRAY-BUHFOSPRSA-N

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Descrição geral

2,2′-Azobis(2-methylbutyronitrile), also known as AIBN, 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).

Aplicação

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.

Armazenamento e estabilidade

Warning: these products are subject to the Explosives Act and must be transported refrigerated - additional costs for transport will apply.

Pictogramas

FlameExclamation mark

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

Acute Tox. 4 Oral - Self-react. D

Código de classe de armazenamento

4.1A - Other explosive hazardous materials

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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The behavior of nanogels in suspension can be dramatically affected by the grafting of a canopy of end-tethered polymer chains. The architecture of the interfacial layer, defined by the grafting density and length of the polymer chains, is a crucial
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An alternative approach for the synthesis of styrene butadiene rubber (SBR) copolymer latexes was explored in order to obtain low gel fractions and high solid contents. The ultra-turrax-assisted miniemulsion stabilized by in situ surfactant generation was adopted as the main

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