Skip to Content
Merck
CN

242489

Bromoacetonitrile

97%

Synonym(s):

2-Bromoacetonitrile, Bromomethyl cyanide, Cyanomethyl bromide

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
BrCH2CN
CAS Number:
590-17-0
Molecular Weight:
119.95
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24854561
EC Number:
209-672-1
Beilstein/REAXYS Number:
956569
MDL number:
MFCD00001884
Assay:
97%
Form:
liquid

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

REXUYBKPWIPONM-UHFFFAOYSA-N

InChI

1S/C2H2BrN/c3-1-2-4/h1H2

SMILES string

BrCC#N

assay

97%

form

liquid

Quality Level

200

bp

60-62 °C/24 mmHg (lit.)

density

1.722 g/mL at 25 °C (lit.)

functional group

bromo, nitrile

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Bromoacetonitrileis an organic compound, generally used as a cyanoalkyl source. It is also used in organic synthesis as a chemical intermediate and an alkylating agent.

Application

Bromoacetonitrile was used in the synthesis of 1-cyanomethyl-1,1-dimethylhydrazinium bromide.

pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SDBB7253
SDBB1192
SDBB1191
STBL2417
STBL1154

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

Synthesis of 4-cyanoethylated benzoxazines by visible-light-promoted radical oxycyanomethylation of olefinic amides with bromoacetonitrile
Sun S, et al.
Tetrahedron Letters, 60(33), 150926-150926 (2019)
The synthesis of three novel pendant armed macrocyclic ligands. The X-ray crystal structure of a cadmium complex derived from the first oxaazamacrocycle bearing two alkylated aromatic amine functions
Valencia L, et al.
Polyhedron, 20(26-27), 3091-3099 (2001)
Carles Miró Sabaté et al.
Chemistry, an Asian journal, 7(5), 1085-1095 (2012-03-03)
1,1-Dimethylhydrazine can be readily alkylated with bromoacetonitrile to form 1-cyanomethyl-1,1-dimethylhydrazinium bromide ([(CH(3))(2)N(CH(2)CN)NH(2)]Br, 1). The metathesis reaction of compound 1 led to the formation of a new family of energetic salts based on the [(CH(3))(2)N(CH(2)CN)NH(2)](+) cation and nitrate (2), perchlorate (3)

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