Skip to Content
Merck
CN
All Photos(1)

Documents

Safety Information

11596

Sigma-Aldrich

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

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C10H16N4
CAS Number:
13472-08-7
Molecular Weight:
192.26
Beilstein:
1710306
EC Number:
236-740-8
MDL number:
MFCD00080408
UNSPSC Code:
12352102
PubChem Substance ID:
57646935
NACRES:
NA.22

Quality Level

200

Assay

≥98.0%

form

solid

mp

49-52 °C

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

Looking for similar products? Visit Product Comparison Guide

General description

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).

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.

Storage and Stability

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

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H242,H302

Hazard Classifications

Acute Tox. 4 Oral - Self-react. D

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Young-Gon Kim et al.
Polymers, 12(8) (2020-08-23)
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
Julius Müller et al.
Acta biomaterialia, 71, 420-431 (2018-03-11)
The interaction of nanocarriers with blood plasma components influences the biological response, and therefore, it needs to be controlled. Whereas protein adsorption to nanocarriers has been investigated to a large extent, the role of lipid interaction for drug delivery and
Anderson M S Medeiros et al.
Polymers, 12(7) (2020-07-08)
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
Lisa Landgraf et al.
Scientific reports, 7(1), 4341-4341 (2017-07-01)
All over the world, different types of nanomaterials with a diversified spectrum of applications are designed and developed, especially in the field of nanomedicine. The great variety of nanoparticles (NPs), in vitro test systems and cell lines led to a

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service