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101281

Sigma-Aldrich

3-Bromopropionic acid

97%

Synonym(s):

2-Carboxyethyl bromide, 3-Bromopropanoic acid, beta-bromopropionic acid

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About This Item

Linear Formula:
BrCH2CH2COOH
CAS Number:
590-92-1
Molecular Weight:
152.97
Beilstein/REAXYS Number:
1071333
EC Number:
209-694-1
MDL number:
MFCD00002763
UNSPSC Code:
12352100
PubChem Substance ID:
24846536
NACRES:
NA.22

assay

97%

mp

58-62 °C (lit.)

density

1.48 g/mL at 25 °C (lit.)

SMILES string

OC(=O)CCBr

InChI

1S/C3H5BrO2/c4-2-1-3(5)6/h1-2H2,(H,5,6)

InChI key

DHXNZYCXMFBMHE-UHFFFAOYSA-N

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Application

Quaternization agent in amperometric biosensors. Alkylates mercaptans and other sulfur containing compounds.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

150.8 °F - closed cup

flash_point_c

66 °C - closed cup

ppe

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

Certificates of Analysis (COA)

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R L Brown et al.
Biochemistry, 32(38), 10089-10095 (1993-09-28)
Analogs of cGMP bearing diverse substituents at the C8 position of the guanine ring system have been shown to activate the cGMP-activated channel of retinal rods at concentrations lower than cGMP itself. In an effort to understand this behavior, we
Mona Doshi et al.
Molecular pharmacology, 95(5), 475-489 (2019-03-08)
Near-infrared (NIR) imaging is a promising technique for use as a noninvasive and sensitive diagnostic tool. Although the NIR fluorescently labeled glucose analog glucosamine (cypate-glucosamine) has applications in preclinical imaging, the transport pathways and fate of this probe in tissues
Synthetic Communications, 23, 373-373 (1993)
B A Gregg et al.
Analytical chemistry, 62(3), 258-263 (1990-02-01)
Oxidoreductases, such as glucose oxidase, can be electrically "wired" to electrodes by electrostatic complexing or by covalent binding of redox polymers so that the electrons flow from the enzyme, through the polymer, to the electrode. We describe two materials for
V K Chadha et al.
Biochemistry, 23(2), 216-221 (1984-01-17)
Horse liver alcohol dehydrogenase is inactivated with Michaelis kinetics at pH 7 and 25 degrees C by 3-bromopropionic acid. In the absence of NAD+, the Ki is 2 mM, and the pseudo bimolecular rate constant (k3/Ki) is 0.03 M-1 s-1;
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