18180
3-Bromopropionic acid
puriss., ≥99.0% (GC)
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About This Item
Linear Formula:
BrCH2CH2COOH
CAS Number:
Molecular Weight:
152.97
EC Number:
209-694-1
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1071333
MDL number:
InChI key
DHXNZYCXMFBMHE-UHFFFAOYSA-N
InChI
1S/C3H5BrO2/c4-2-1-3(5)6/h1-2H2,(H,5,6)
SMILES string
OC(=O)CCBr
grade
puriss.
assay
≥99.0% (GC)
mp
60-64 °C
solubility
H2O: 0.1 g/mL, clear
density
1.48 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Other Notes
Alkylates the ε-amino group of lysine in proteins
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
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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Selective modification of the mitochondrial isozyme of aspartate aminotransferase by -bromopropionate. I. Inactivation process and properties of inactivated enzyme.
M Okamoto et al.
Biochemistry, 11(17), 3188-3195 (1972-08-15)
M A Lea et al.
Anticancer research, 18(4A), 2717-2722 (1998-08-15)
The relationship between histone acetylation and induction of gene expression was studied in Ros 17/2.8 rat osteosarcoma cells transfected with the pCH110 plasmid. This plasmid is commonly used in cotransfections as a measure of transfection efficiency. Cells were incubated for
Iwona Kowałczyk
Acta chimica Slovenica, 61(1), 39-50 (2014-03-26)
3-(3-Dimethylammonio)propylammonio propanoate bromide (1), 4-(3-dimethylammonio)propylammonio butanoate bromide (2), and 5-(3-dimethylammonio)propylammonio pentanoate bromide (3) have been obtained in reaction of 1,1-dimethyl-1,3-propylenediamine with 3-bromopropionic acid, ethyl 4-bromobutyrate and 5-bromovaleric acid, respectively. The products have been characterized by FTIR, Raman and NMR spectroscopy.
Patrick Giraudeau et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 190(2), 339-345 (2007-12-18)
Recent ultrafast techniques enable nD NMR spectra to be obtained in a single scan. However, resolution enhancement in the ultrafast domain leads to important sensitivity losses and lineshape distortions. In order to understand better resolution and spatial encoding aspects of
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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