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Merck
CN

24510

Chloroacetic acid

puriss., ≥99.0% (T)

Synonym(s):

Monochloroacetic acid

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About This Item

Linear Formula:
ClCH2COOH
CAS Number:
Molecular Weight:
94.50
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
201-178-4
Beilstein/REAXYS Number:
605438
MDL number:
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vapor density

3.26 (vs air)

vapor pressure

0.75 mmHg ( 20 °C)

grade

puriss.

assay

≥99.0% (T)

form

solid

ign. residue

≤0.05%

bp

189 °C (lit.)

mp

60-63 °C

SMILES string

CC(C)C[C@@H](N(C)C(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O, OC(=O)CCl

InChI

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

InChI key

FOCAUTSVDIKZOP-UHFFFAOYSA-N

Other Notes

Reagent for the gravimetric det. of zirconium


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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

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

Regulatory Information

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G. Norwitz
Analytica Chimica Acta, 35, 491-491 (1966)
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



Global Trade Item Number

SKUGTIN
515000-5G04061831820546