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18165

Sigma-Aldrich

(R)-(+)-2-Bromopropionic acid

≥98.0% (sum of enantiomers, GC)

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About This Item

Empirical Formula (Hill Notation):
C3H5BrO2
CAS Number:
10009-70-8
Molecular Weight:
152.97
Beilstein/REAXYS Number:
1720262
MDL number:
MFCD00145205
UNSPSC Code:
12352101
PubChem Substance ID:
57647718
NACRES:
NA.22

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

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H302,H314

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

212.0 °F - closed cup

flash_point_c

100 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

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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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