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291773

Sigma-Aldrich

Sodium chloroacetate

98%

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Synonym(s):
Chloroacetic acid sodium salt
Linear Formula:
ClCH2COONa
CAS Number:
3926-62-3
Molecular Weight:
116.48
Beilstein:
3597157
EC Number:
223-498-3
MDL number:
MFCD00002684
PubChem Substance ID:
329753318
NACRES:
NA.55

Quality Level

200

Assay

98%

form

powder or chunks

mp

199 °C (dec.) (lit.)

SMILES string

[Na+].[O-]C(=O)CCl

InChI

1S/C2H3ClO2.Na/c3-1-2(4)5;/h1H2,(H,4,5);/q;+1/p-1

InChI key

FDRCDNZGSXJAFP-UHFFFAOYSA-M

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1 of 4

This Item
347795L7022456020
Sodium chloroacetate 98%

Sigma-Aldrich

291773

Sodium chloroacetate

Sodium dichloroacetate 98%

Sigma-Aldrich

347795

Sodium dichloroacetate

Sodium L-lactate ~98%

Sigma-Aldrich

L7022

Sodium L-lactate

Sodium formate 99.998% trace metals basis

Sigma-Aldrich

456020

Sodium formate

form

powder or chunks

form

-

form

powder or crystals

form

powder and chunks

mp

199 °C (dec.) (lit.)

mp

198 °C (dec.) (lit.)

mp

163-165 °C (lit.)

mp

259-262 °C (lit.)

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H301 - H315 - H319 - H400

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

6.1D - Non-combustible, acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 3

Flash Point(F)

518.0 °F

Flash Point(C)

270 °C

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Aliev et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 6(7), 1120-1126 (2000-04-29)
The thermally induced solidstate polymerization reactions in sodium chloroacetate and sodium bromoacetate, leading to poly(hydroxyacetic acid) (polyglycolide) and NaCl and NaBr, respectively, were studied by isothermal in situ solid-state NMR spectroscopy at 120, 130 and 140 degrees C with a
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In this study, a fluorescence resonance energy transfer (FRET) immunoassay based on graphene oxide (GO) and up-converting nanoparticles (UCNPs) was established for rapid detection of imidacloprid, a commonly-used insecticide. Under 980 nm near-infrared light excitation, emission of UCNPs at 542 nm can
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The reaction of 3-(1-adamantyl)-4-substituted-1,2,4-triazoline-5-thiones 3a-g with sodium chloroacetate, in ethanolic sodium hydroxide yielded the corresponding N1-acetic acid derivatives 4a-g. The interaction of 3a-g with ethyl 2-bromopropionate in acetone, in the presence of potassium carbonate, yielded the corresponding N1-ethyl propionate derivatives
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