Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C10H16N4
CAS Number:
Molecular Weight:
192.26
UNSPSC Code:
12352102
NACRES:
NA.22
PubChem Substance ID:
EC Number:
236-740-8
Beilstein/REAXYS Number:
1710306
MDL number:
Assay:
≥98.0%
Form:
solid
Quality Level
assay
≥98.0%
form
solid
mp
49-52 °C
functional group
azo, nitrile
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
General description
2,2′-Azobis(2-methylbutyronitrile), also known as AMBN, 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.
Preparation Note
Warning: these products are subject to the Explosives Act and must be transported refrigerated - additional costs for transport will apply.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Self-react. D
Storage Class
4.1A - Other explosive hazardous materials
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 277908-1KG | 04061833366080 |
| 277908-20G | 04061826202197 |
| 277908-5G | 04061835561964 |
| 277908-100G | 04061826202180 |
| 11596-250G | 04061833554289 |
| 11596-50G | 04061833554296 |

