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132691

Sigma-Aldrich

3-Chloropropionic acid

98%

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About This Item

Fórmula lineal:
ClCH2CH2COOH
Número de CAS:
107-94-8
Peso molecular:
108.52
Beilstein/REAXYS Number:
1098495
EC Number:
203-534-4
MDL number:
MFCD00002764
UNSPSC Code:
12352100
PubChem Substance ID:
24848067
NACRES:
NA.22

Quality Level

100

assay

98%

form

solid

bp

203-205 °C (lit.)

mp

35-40 °C (lit.)

solubility

H2O: soluble 50 mg/mL, clear, colorless

functional group

carboxylic acid
chloro

SMILES string

OC(=O)CCCl

InChI

1S/C3H5ClO2/c4-2-1-3(5)6/h1-2H2,(H,5,6)

InChI key

QEYMMOKECZBKAC-UHFFFAOYSA-N

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General description

3-Chloropropionic acid is used in pesticides.

Application

3-Chloropropionic acid was used to study the degradation of 3-chloropropionic acid by Pseudomonas sp. strain isolated from rice paddy fields. It was also used in determination of 3-bromopropionic acid, biomarker for the exposure to 1-bromopropane in human urine by gas chromatography.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1A

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 1

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificados de análisis (COA)

Lot/Batch Number
STBB0440V
STBB0440
STBB0160V
STBB0160
S88704

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Degradation of 3-chloropropionic acid (3CP) byPseudomonas sp. B6P isolated from a rice paddy field.
Mesri S, et al.
Annals of Microbiology, 59(3), 447-451 (2009)
Gang Cheng et al.
International journal of nanomedicine, 7, 3991-4006 (2012-08-21)
The reduction-sensitive cationic polymer is a promising nonviral carrier for gene delivery. Until now, disulfide bonds have been the only golden standard for its design. The aim of this research was to develop a novel reduction-responsive cationic polymer as a
S J Armfield et al.
Biodegradation, 6(3), 237-246 (1995-09-01)
Rhodococcus erythropolis Y2 produced two types of dehalogenase: a hydrolytic enzyme, that is an halidohydrolase, which was induced by C3 to C6 1-haloalkane substrates, and at least one oxygenase-type dehalogenase induced by C7 to C16 1-haloalkanes and n-alkanes. The oxygenase-type
Wanwen Chen et al.
International journal of biological macromolecules, 173, 504-512 (2021-01-19)
Synthetic selenium polysaccharides with potential bioactivity have drawn great interest due to the SeO bonds existing in the structure. Herein, N, O-selenized N-(2-carboxyethyl) chitosan (sNCCS) was synthesized through carboxyethylation and selenylation. Various characterizations were performed to identify the structure of
C Rottleb et al.
International journal of cancer, 67(5), 724-729 (1996-09-04)
Terminal differentiation of hematopoietic cells in vivo and in vitro is almost invariably accompanied by down-regulated expression of the c-myc proto-oncogene. Constitutive expression of c-myc in tumor cells inhibits terminal differentiation and maintains proliferation. In Burkitt's lymphoma, chromosomal translocations cause
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