Skip to Content
Merck
All Photos(1)

Documents

109231

Sigma-Aldrich

3-Bromopropionitrile

≥98.0% (GC)

Synonym(s):

3-Bromopropanenitrile

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
BrCH2CH2CN
CAS Number:
Molecular Weight:
133.97
Beilstein:
1738565
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

≥98.0% (GC)

refractive index

n20/D 1.481 (lit.)

bp

76-78 °C/10 mmHg (lit.)

density

1.615 g/mL at 25 °C (lit.)

SMILES string

BrCCC#N

InChI

1S/C3H4BrN/c4-2-1-3-5/h1-2H2

InChI key

CQZIEDXCLQOOEH-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

3-Bromopropionitrile was used as the initiator in the atom transfer radical polymerization of acrylonitrile. 3-Bromopropionitrile was used in coupling reactions of a number of aromatic and heteroaromatic phenols with alkyl, acyl or benzoyl halides in acetonitrile with cesium fluoride-Celite.

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 2 Oral

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

206.6 °F - closed cup

Flash Point(C)

97 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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

Cesium fluoride-Celite: a solid base for efficient syntheses of aromatic esters and ethers.
Shah STA, et al.
Tetrahedron, 61(27), 6652-6656 (2005)
Preparation of polyacrylonitrile with improved isotacticity and low polydispersity.
Jiang J, et al.
Journal of Applied Polymer Science, 116(5), 2610-2616 (2010)

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