18165
(R)-(+)-2-Bromopropionic acid
≥98.0% (sum of enantiomers, GC)
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About This Item
Empirical Formula (Hill Notation):
C3H5BrO2
CAS Number:
Molecular Weight:
152.97
Beilstein:
1720262
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
≥98.0% (sum of enantiomers, GC)
form
liquid
optical activity
[α]20/D +26±2°, neat
refractive index
n20/D 1.475
density
1.692 g/mL at 20 °C (lit.)
storage temp.
2-8°C
SMILES string
C[C@@H](Br)C(O)=O
InChI
1S/C3H5BrO2/c1-2(4)3(5)6/h2H,1H3,(H,5,6)/t2-/m1/s1
InChI key
MONMFXREYOKQTI-UWTATZPHSA-N
Related Categories
Caution
may discolor to brownish on storage
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
WGK
WGK 3
Flash Point(F)
212.0 °F
Flash Point(C)
100 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Eugénie Grigorian et al.
Frontiers in microbiology, 12, 725997-725997 (2021-10-09)
L-2-halocid dehalogenases (L-2-HADs) have been mainly characterized from terrestrial polluted environments. By contrast, knowledge is still scarce about their role in detoxification of predominant halocarbons in marine environments. Here, phylogenetic analyses showed a wide diversity of homologous L-2-HADs, especially among
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