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101281

Sigma-Aldrich

3-Bromopropionic acid

97%

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Synonym(s):
2-Carboxyethyl bromide, 3-Bromopropanoic acid, beta-bromopropionic acid
Linear Formula:
BrCH2CH2COOH
CAS Number:
Molecular Weight:
152.97
Beilstein/REAXYS Number:
1071333
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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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1 of 4

This Item
B78300B56307282456
3-Bromopropionic acid 97%

101281

3-Bromopropionic acid

2-Bromopropionic acid 99%

B78300

2-Bromopropionic acid

Bromoacetic acid reagent grade, 97%

B56307

Bromoacetic acid

2-Bromopropionic acid-1-13C 99 atom % 13C

282456

2-Bromopropionic acid-1-13C

density

1.48 g/mL at 25 °C (lit.)

density

1.7 g/mL at 25 °C (lit.)

density

-

density

1.7 g/mL at 25 °C (lit.)

mp

58-62 °C (lit.)

mp

-

mp

47-49 °C (lit.)

mp

-

Application

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

pictograms

Corrosion

signalword

Danger

hcodes

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


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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
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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
B A Gregg et al.
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Synthetic Communications, 23, 373-373 (1993)
V K Chadha et al.
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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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