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24520

Sigma-Aldrich

Chloroacetic acid

purum, ≥97.0% (T)

Synonym(s):

Monochloroacetic acid

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About This Item

Linear Formula:
ClCH2COOH
CAS Number:
Molecular Weight:
94.50
Beilstein/REAXYS Number:
605438
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

vapor density

3.26 (vs air)

vapor pressure

0.75 mmHg ( 20 °C)

grade

purum

assay

≥97.0% (T)

form

solid

ign. residue

≤0.1%

bp

189 °C (lit.)

mp

60-63 °C (lit.)
61-64 °C

SMILES string

OC(=O)CCl

InChI

1S/C2H3ClO2/c3-1-2(4)5/h1H2,(H,4,5)

InChI key

FOCAUTSVDIKZOP-UHFFFAOYSA-N

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signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

258.8 °F - closed cup

flash_point_c

126 °C - closed cup

ppe

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


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The crystal and molecular structures of trinuclear vanadium and chromium complexes with chloroacetic acid.
Glowiak T, et al.
Bulletin de l'Academie Polonaise des Sciences. Serie des Sciences Chimiques, 25(5), 359-371 (1977)
Yang Yu et al.
Bioorganic & medicinal chemistry letters, 17(12), 3508-3510 (2007-05-11)
A simple and effective synthesis of 3,4-dihydropyrimidin-2(1H)-one derivatives from aldehydes, 1,3-dicarbonyl compounds and urea or thiourea using chloroacetic acid as catalyst under solvent-free conditions is described. Compared with the classical Biginelli reaction conditions, this new method has the advantage of
The use of chloroacetic acid in the mitsunobu reaction.
Saiah M, et al.
Tetrahedron Letters, 33(30), 4317-4320 (1992)
Brendon Y Chua et al.
Molecular pharmaceutics, 9(1), 81-90 (2011-12-14)
It has become increasingly recognized that polymer particle size can have a profound effect on the interactions of particle-based vaccines with antigen presenting cells (APCs) thereby influencing and modulating ensuing immune responses. With the aim of developing chitosan particle-based immunocontraceptive
Maike M Schmidt et al.
Neurotoxicity research, 19(4), 628-637 (2010-07-16)
The chlorinated acetates monochloroacetate (MCA), dichloroacetate (DCA), and trichloroacetate (TCA) are generated in water disinfection processes and are formed during metabolic detoxification of industrial solvents such as trichloroethylene. In order to test for consequences of an exposure of brain cells

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