18180
3-Bromopropionic acid
puriss., ≥99.0% (GC)
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About This Item
Linear Formula:
BrCH2CH2COOH
CAS Number:
Molecular Weight:
152.97
Beilstein:
1071333
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
grade
puriss.
Assay
≥99.0% (GC)
mp
58-62 °C (lit.)
60-64 °C
solubility
H2O: 0.1 g/mL, clear
density
1.48 g/mL at 25 °C (lit.)
storage temp.
2-8°C
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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Other Notes
Alkylates the ε-amino group of lysine in proteins
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
150.8 °F - closed cup
Flash Point(C)
66 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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
Patrick Giraudeau et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 186(2), 352-357 (2007-04-03)
Recent ultrafast techniques enable 2D NMR spectra to be obtained in a single scan. A modification of the detection scheme involved in this technique is proposed, permitting the achievement of 2D 1H J-resolved spectra in 500 ms. The detection gradient
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;
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.
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