Key Documents

View All Documentation

01-7220

2,2′-Azobis(2-methylpropionitrile)

Name: 2,2′-Azobis(2-methylpropionitrile)
Brand: SAJ

SAJ first grade, ≥98.0%

Synonym(s):

α,α′-Azoisobutyronitrile, AIBN, Azobisisobutyronitrile, Free radical initiator

Select a Size

Change View

About This Item

Linear Formula:

(CH₃)₂C(CN)N=NC(CH₃)₂CN

CAS Number:

78-67-1

Molecular Weight:

164.21

EC Number:

201-132-3

UNSPSC Code:

12352102

PubChem Substance ID:

329747353

Beilstein/REAXYS Number:

1708400

MDL number:

MFCD00013808

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

grade

SAJ first grade

assay

≥98.0%

availability

available only in Japan

mp

102-104 °C (dec.) (lit.)

SMILES string

CC(C)(\N=N\C(C)(C)C#N)C#N

InChI

1S/C8H12N4/c1-7(2,5-9)11-12-8(3,4)6-10/h1-4H3/b12-11+

InChI key

OZAIFHULBGXAKX-VAWYXSNFSA-N

Description

Still not finding the right product?

Explore all of our products under 2,2′-Azobis(2-methylpropionitrile)

pictograms

GHS02,GHS07

signalword

Danger

hcodes

H242,H302 + H332,H412

pcodes

P210 - P235 - P273 - P304 + P340 + P312 - P370 + P378 - P403

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Self-react. C

supp_hazards

EUH044

Storage Class

4.1A - Other explosive hazardous materials

wgk

WGK 2

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Azobisisobutyronitrile initiated aerobic oxidative transformation of amines: coupling of primary amines and cyanation of tertiary amines.

Lianghui Liu et al.

Organic letters, 14(22), 5692-5695 (2012-10-31)

In the presence of a catalytic amount of radical initiator AIBN, primary amines are oxidatively coupled to imines and tertiary amines are cyanated to α-aminonitriles. These "metal-free" aerobic oxidative coupling reactions may find applications in a wide range of "green"

A novel urethane acrylate-based root canal sealer with improved degree of conversion, cytotoxicity, bond strengths, solubility, and dimensional stability.

Bor-Shiunn Lee et al.

Journal of endodontics, 37(2), 246-249 (2011-01-18)

We have developed new urethane acrylate-based root canal sealers using polycarbonate (PC) as polyol and 2,2-azobis(2-methyl)butyronitrile (AMBN) as a thermal initiator. The purpose of this study was to compare the properties among a group of seven sealers: (1) polybutyleneadipate (PBA)

Uniform PEO star polymers synthesized in water via free radical polymerization or atom transfer radical polymerization.

Wenwen Li et al.

Macromolecular rapid communications, 32(1), 74-81 (2011-03-25)

Amphiphilic star shaped polymers with poly(ethylene oxide) (PEO) arms and cross-linked hydrophobic core were synthesized in water via either conventional free radical polymerization (FRP) or atom transfer radical polymerization (ATRP) techniques using a simple "arm-first" method. In FRP, PEO based

View All Related Papers

Global Trade Item Number

SKU	GTIN
01-7220-2-25G-J	04061832683362
01-7220-5-500G-J	04061832683379