Skip to Content
Merck
CN
All Photos(1)

Documents

Safety Information

24510

Sigma-Aldrich

Chloroacetic acid

puriss., ≥99.0% (T)

Sign Into View Organizational & Contract Pricing

Synonym(s):
Monochloroacetic acid
Linear Formula:
ClCH2COOH
CAS Number:
Molecular Weight:
94.50
Beilstein:
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

puriss.

Assay

≥99.0% (T)

form

solid

ign. residue

≤0.05%

bp

189 °C (lit.)

mp

60-63 °C (lit.)
60-63 °C

SMILES string

OC(=O)CCl

InChI

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

InChI key

FOCAUTSVDIKZOP-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Other Notes

Reagent for the gravimetric det. of zirconium

replaced by

Product No.
Description
Pricing

Signal Word

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

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
The use of chloroacetic acid in the mitsunobu reaction.
Saiah M, et al.
Tetrahedron Letters, 33(30), 4317-4320 (1992)
Devang Odedra et al.
Acta biomaterialia, 7(8), 3027-3035 (2011-05-24)
A key challenge in tissue engineering is overcoming cell death in the scaffold interior due to the limited diffusion of oxygen and nutrients therein. We here hypothesize that immobilizing a gradient of a growth/survival factor from the periphery to the

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service