Sigma-Aldrich 402923 Chloroacetic acid ACS reagent, ≥99.0% CAS No.: 79-11-8 2 kg
Category
Brand
Stock Code
LB.SA.402923-2KG
Kısa Bilgi
Synonym(s): Monochloroacetic acid Linear Formula: ClCH2COOH CAS Number: 79-11-8 Molecular Weight: 94.50 Beilstein: 605438 EC Number: 201-178-4 MDL number: MFCD00002683
| Sigma-Aldrich 402923 Chloroacetic acid ACS reagent, ≥99.0% 2 kg |
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Synonym(s): Monochloroacetic acid
Linear Formula: ClCH2COOH
CAS Number: 79-11-8
Molecular Weight: 94.50
Beilstein: 605438
EC Number: 201-178-4
MDL number: MFCD00002683
PubChem Substance ID: 24865140
NACRES: NA.21
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PROPERTIES
grade ACS reagent
Quality Level 200
vapor density 3.26 (vs air)
vapor pressure 0.75 mmHg (20 °C)
assay ≥99.0%
form solid
impurities
≤0.01% Carbonyl compounds (as acetone)
≤0.01% Carbonyl compunds (other than acetone)
≤0.01% insolubles
ign. residue <0.02%
bp 189 °C (lit.)
mp 60-63 °C (lit.)
solubility water: soluble 3170 g/L at 10 °C
anion traces
chloride (Cl-): ≤0.01%
sulfate (SO42-): ≤0.02%
cation traces
Fe: ≤0.002%
heavy metals: ≤0.001% (by ICP)
SMILES string OC(=O)CCl
InChI 1S/C2H3ClO2/c3-1-2(4)5/h1H2,(H,4,5)
InChI key FOCAUTSVDIKZOP-UHFFFAOYSA-N
DESCRIPTION
General description
Chloroacetic acid (CAA, monochloroacetic acid, MCAA) is a halogenated aliphatic carboxylic acid generally used as herbicide and preservative. Its mutagenic effects have been studied in Rattus norvegicus.[1] The rate of degradation of MCA by photocatalysis using TiO2 at pH3 is reported to be enhanced under the influence of ozone.[2] CAA is an irritant that hydrolyzes proteins resulting in degradation of the cells. This property has been applied in treating plantar warts.[3]
Application
Chloroacetic acid may be used to synthesize the following:
Thiocarbamoylthioacetic acid derivatives.[4]
4-Thiazolone derivatives.[5]
Triazinothiazolone derivatives.[6]
Water soluble carboxymethyl chitosan.[7]
Packaging
100, 500 g in poly bottle
2 kg in poly bottle
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