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About This Item
Fórmula empírica (notación de Hill):
C8H12N4
Número CAS:
Peso molecular:
164.21
UNSPSC Code:
12162002
PubChem Substance ID:
MDL number:
Nombre del producto
Azobisisobutyronitrile, 12 wt. % in acetone
InChI
1S/C8H12N4/c1-7(2,5-9)11-12-8(3,4)6-10/h1-4H3/b12-11+
SMILES string
CC(C)(\N=N\C(C)(C)C#N)C#N
InChI key
OZAIFHULBGXAKX-VAWYXSNFSA-N
form
liquid
concentration
12 wt. % in acetone
refractive index
n20/D 1.368
density
0.808 g/mL at 25 °C
storage temp.
2-8°C
Quality Level
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Categorías relacionadas
Application
- Used as an initiator in the synthesis of highly cross-linked Poly(divinylbenzene) (PDVB) polymers.
- Used as an initiator in the polymerization process of 2-hydroxyethyl methacrylate (HEMA).
Features and Benefits
Decomposes unimolecularly at good rates without much variation from one solvent to another.
General description
Azobisisobutyronitrile (AIBN) is an azo-compound and is widely used as a free radical initiator. This compound has labile carbon-nitrogen covalent bond which undergoes homolytic scission under thermal, chemical or photochemical conditions producing free radicals. They are useful in many reactions like halogenation, polymerisation of vinyl monomers, grafting reactions, curing of rubbers and unsaturated polymers and cross-linking of polyolefins.
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
target_organs
Respiratory system
supp_hazards
Clase de almacenamiento
3 - Flammable liquids
wgk
WGK 2
flash_point_f
1.4 °F
flash_point_c
-17 °C
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Biomaterials based on 2-hydroxyethyl methacrylate: the influence of the initiator type
Nita, L. E., Chiriac, A. P., Nistor, M. T., & Stoica, I.
Rev. Roum. Chim., 56(5), 537-543 (2011)
Initiator efficiency in radical polymerization
Walling, C.
Journal of Polymer Science, 14(74), 214-217 (1954)
Synthesis of highly cross-linked polymers in supercritical carbon dioxide by heterogeneous polymerization.
Cooper, A. I., Hems, W. P., & Holmes, A. B.
Macromolecules, 32(7), 2156-2166 (1999)
Selected radical azoinitiators in the synthesis of solvent-borne acrylic pressure-sensitive adhesives
Pabin-Szafko, B., Wisniewska, E., & Czech, Z.
Chemistry and Chemical Technology, 3(2), 101-106 (2009)
E K Efthimiadou et al.
International journal of pharmaceutics, 428(1-2), 134-142 (2012-03-10)
In the current study, poly lactic acid (PLA) modified hollow crosslinked poly(hydroxyethyl methacrylate) (PHEMA) microspheres have been prepared, in order to obtain a stimulus-responsive, biocompatible carrier with sustained drug release properties. The synthetical process consisted of the preparation of poly(methacrylic
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