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Merck
CN

132691

3-Chloropropionic acid

98%

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About This Item

Linear Formula:
ClCH2CH2COOH
CAS Number:
107-94-8
Molecular Weight:
108.52
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848067
EC Number:
203-534-4
Beilstein/REAXYS Number:
1098495
MDL number:
MFCD00002764

Key Documents

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Product Name

3-Chloropropionic acid, 98%

InChI key

QEYMMOKECZBKAC-UHFFFAOYSA-N

InChI

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

SMILES string

OC(=O)CCCl

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

Quality Level

100

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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.

General description

3-Chloropropionic acid is used in pesticides.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1A

Storage Class

8A - Combustible corrosive hazardous materials

wgk

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

Regulatory Information

危险化学品
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Certificates of Analysis (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
Alba T Macias et al.
Bioorganic & medicinal chemistry, 12(7), 1643-1647 (2004-03-19)
Gamma-Hydroxybutyric acid (GHB) has gained in notoriety in recent years due to its association with sexual assaults. GHB is an endogenous ligand for GHB receptors, but its complete pharmacological mechanism of action in vivo remains unclear due to apparent GABAergic
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
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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