291773
Sodium chloroacetate
98%
Synonym(s):
Chloroacetic acid sodium salt
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About This Item
Linear Formula:
ClCH2COONa
CAS Number:
Molecular Weight:
116.48
Beilstein/REAXYS Number:
3597157
EC Number:
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.55
Quality Level
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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Related Categories
Application
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- Effective extraction of fluoroquinolones from water using facile modified plant fibers.: This article investigates the use of modified plant fibers for the efficient extraction of fluoroquinolones from water, highlighting the utility of sodium chloroacetate in the modification process (Zhang et al., 2022).
- Sodium Chloroacetate Modified Polyethyleneimine/Trimesic Acid Nanofiltration Membrane to Improve Antifouling Performance.: The study details the improvement of antifouling performance in nanofiltration membranes through modification with sodium chloroacetate (Gu et al., 2021).
- Preparation of BiOCl/Bi(2)WO(6) Photocatalyst for Efficient Fixation on Cotton Fabric: Applications in UV Shielding and Self-Cleaning Performances.: This research focuses on the application of a BiOCl/Bi(2)WO(6) photocatalyst in UV shielding and self-cleaning performances on cotton fabric, employing sodium chloroacetate in the preparation process (Chen et al., 2021).
signalword
Danger
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
6.1D - Non-combustible, acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
wgk_germany
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
Omar A Al-Deeb et al.
Arzneimittel-Forschung, 56(1), 40-47 (2006-02-16)
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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