Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

More Documents

B81204

Sigma-Aldrich

Bromosuccinic acid

98%

Synonym(s):

2-Bromobutanedioic acid, 2-Bromosuccinic acid, DL-Bromosuccinic acid, Monobromosuccinic acid

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
HOOCCH2CHBrCOOH
CAS Number:
923-06-8
Molecular Weight:
196.98
Beilstein:
1723556
EC Number:
213-087-7
MDL number:
MFCD00004213
UNSPSC Code:
12352100
PubChem Substance ID:
24892047
NACRES:
NA.22

Quality Level

100

Assay

98%

form

powder

mp

161-163 °C (lit.)

SMILES string

OC(=O)CC(Br)C(O)=O

InChI

1S/C4H5BrO4/c5-2(4(8)9)1-3(6)7/h2H,1H2,(H,6,7)(H,8,9)

InChI key

QQWGVQWAEANRTK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315 - H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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

M Blumrich et al.
Biochimica et biophysica acta, 1029(1), 1-12 (1990-11-02)
The present study indicates that SH-groups are essential for the uptake of [3H]taurocholate and [14C]cholate into isolated rat hepatocytes. Several sulfhydryl-modifying reagents viz. p-chloromercuribenzenesulfonate (PCMBS), N-ethylmaleimide (NEM), dithio-bis(5-nitropyridine) (DTNP), bromosuccinimide and HgCl2 inhibited uptake of bile acids in a concentration-dependent
R H Yamada et al.
Biochimica et biophysica acta, 801(1), 151-154 (1984-09-07)
DL-Hydrazinosuccinic acid was synthesized by the reaction of DL-bromosuccinic acid with hydrazine. The compound strongly inhibited aspartate aminotransferase and gave 50% inhibition at 1.3 microM when added simultaneously with L-aspartate to an assay mixture containing enzyme. Incubation of the enzyme
Contact dermatitis from alpha-bromomethylparotolylsulfone.
S Kerre et al.
Contact dermatitis, 33(2), 130-130 (1995-08-01)
Modification of three active site lysine residues in the catalytic subunit of aspartate transcarbamylase by D- and L-bromosuccinate.
A M Lauritzen et al.
The Journal of biological chemistry, 257(3), 1312-1319 (1982-02-10)
Hyangmi Kim et al.
Archives of microbiology, 199(4), 597-603 (2016-12-29)
A Gram-negative, aerobic, non-motile, rod-shaped bacterial strain, designated MAB-07

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