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Key Documents

714887

Sigma-Aldrich

2,2′-Azobis(2-methylpropionitrile) solution

0.2 M in toluene

Synonym(s):

α,α,′-Azoisobutyronitrile solution, AIBN solution

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About This Item

Empirical Formula (Hill Notation):
C8H12N4
CAS Number:
Molecular Weight:
164.21
MDL number:
UNSPSC Code:
12352102
PubChem Substance ID:
NACRES:
NA.22

form

liquid

concentration

0.2 M in toluene

refractive index

n20/D 1.495

density

0.858 g/mL at 25 °C

storage temp.

2-8°C

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

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Application

2,2′-Azobis(2-methylpropionitrile) (AIBN) is a radical initiator. AIBN solution can be used to initiate radical-induced reactions, specifically free-radical polymerizations. It can be used in:
  • Synthesis of styrene-vinyl pyridine diblock copolymers by reversible addition-fragmentation chain transfer (RAFT) polymerization.
  • Preparation of silicon oxycarbide glasses.
  • Synthesis of poly [N-(p-vinyl benzyl) phthalimide] for the preparation of titanium dioxide composites for electrophoretic displays.

Signal Word

Danger

Hazard Classifications

Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3

Target Organs

Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

39.9 °F

Flash Point(C)

4.4 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Stable titanium dioxide grafted with poly [N-(p-vinyl benzyl) phthalimide] composite particles in suspension for electrophoretic displays.
Dai R, et al.
Colloid and Polymer Science, 289(4), 401-407 (2011)
Optimization of sol?gel/pyrolysis routes to silicon oxycarbide glasses.
Strachota A, et al.
Journal of Non-Crystalline Solids, 358(20), 2771-2782 (2012)
Aspects of the chemistry of azobisisobutyronitrile.
Bevington J C.
Journal of Polymer Science, 10(3), 195-202 (1993)
Styrene?vinyl pyridine diblock copolymers: Synthesis by RAFT polymerization and self?assembly in solution and in the bulk.
Zamfir M, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 50(8), 1636-1644 (2012)
Brandon Lynch et al.
Journal of biomedical materials research. Part B, Applied biomaterials, 105(7), 1863-1873 (2016-05-31)
Cartilage repair presents a daunting challenge in tissue engineering applications due to the low oxygen conditions (hypoxia) affiliated in diseased states. Hence, the use of biomaterial scaffolds with unique variability is imperative to treat diseased or damaged cartilage. Thermosensitive hydrogels

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