Skip to Content
MilliporeSigma

17000

Sigma-Aldrich

Bromoacetic acid

ReagentPlus®, ≥99.0%

Synonym(s):

α-Bromoacetic acid, Monobromoacetic acid

Sign Into View Organizational & Contract Pricing

Select a Size

About This Item

Linear Formula:
BrCH2COOH
CAS Number:
79-08-3
Molecular Weight:
138.95
Beilstein/REAXYS Number:
506167
EC Number:
201-175-8
MDL number:
MFCD00002678
UNSPSC Code:
12352106
PubChem Substance ID:
329751436
NACRES:
NA.22

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

Quality Level

200

product line

ReagentPlus®

assay

≥99.0% (GC)
≥99.0%

form

solid

impurities

≤1% dibromoacetic acid (1H-NMR)

bp

208 °C (lit.)

mp

46-49 °C
47-49 °C (lit.)

solubility

chloroform: 10%, clear, colorless

functional group

bromo
carboxylic acid

SMILES string

NC(=O)C=C
OC(=O)CBr

InChI

1S/C2H3BrO2/c3-1-2(4)5/h1H2,(H,4,5)

InChI key

KDPAWGWELVVRCH-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Bromoacetic acid is mainly used for the N-terminal bromoacylation of resin bound peptides.
It can also be used:
  • To synthesize (Z)-2-(cyclooct-4-en-1-yloxy)acetic acid.
  • To synthesize α-bromo-phenylacetamide.
  • To convert aromatic thiosemicarbazones to thiazolylhydrazones.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Aquatic Acute 1 - Eye Dam. 1 - Skin Corr. 1A - Skin Sens. 1

Storage Class

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

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCN1047
BCCM0401
BCCM5643
BCCH8627
BCCH7021

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

Efficient method for the preparation of peptoids [oligo (N-substituted glycines)] by submonomer solid-phase synthesis.
Zuckermann R N, et al.
Journal of the American Chemical Society, 114(26), 10646-10647 (1992)
Peptide ligation through click chemistry for the generation of assembled and scaffolded peptides.
Franke R, et al.
Tetrahedron Letters, 46(26), 4479-4482 (2005)
Amandine M N Caruana et al.
Marine environmental research, 160, 105014-105014 (2020-09-11)
Alexandrium minutum and Alexandrium pacificum are representatives of the dinoflagellate genus that regularly proliferate on the French coasts and other global coastlines. These harmful species may threaten shellfish harvest and human health due to their ability to synthesize neurotoxic alkaloids
Ryo Kato et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 228, 117656-117656 (2019-11-22)
To sense hydrophilic anions in protic solvents, we fabricated polymethylmethacrylate (PMMA) nanofibers incorporating 4-nitrophenyl azo thiourea polymer as a chromoionophore. When methanol solutions containing anions contacted the PMMA nanofiber, a bathochromic shift from 386 nm was observed in the absorption maximum
Tetrazine?trans-cyclooctene ligation for the rapid construction of 18F labeled probes.
Li Z, et al.
Chemical Communications (Cambridge, England), 46(42), 8043-8045 (2010)
View All Related Papers

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