506877
2-Chlorobenzoic acid
PESTANAL®, analytical standard
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Linear Formula:
ClC6H4CO2H
CAS Number:
Molecular Weight:
156.57
Beilstein/REAXYS Number:
907340
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:
grade
analytical standard
Quality Level
product line
PESTANAL®
packaging
ampule of 1000 mg
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
mp
138-140 °C (lit.)
application(s)
agriculture
environmental
format
neat
storage temp.
room temp
SMILES string
OC(=O)c1ccccc1Cl
InChI
1S/C7H5ClO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,(H,9,10)
InChI key
IKCLCGXPQILATA-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Application
2-Chlorobenzoic acid may be used as a reference standard in the determination of 2-chlorobenzoic acid in water samples using gas chromatography coupled with mass spectrometry (GC-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
343.4 °F
flash_point_c
173 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Experimental design for the study of two derivatization procedures for simultaneous GC analysis of acidic herbicides and water chlorination by-products.
Boucharat C, et al.
Talanta, 47(2), 311-323 (1998)
C A Blackledge et al.
Journal of pharmaceutical and biomedical analysis, 22(6), 1023-1028 (2000-06-17)
The metabolic fate of [14C]-labelled 2 and 4-chlorobenzoic acids (2- and 4-CBA) has been determined in the rat following intraperitoneal (i.p.) administration at 100 mg/kg to male rats. The major route of elimination for both 2-and 4-CBA was urine with
W J Hickey et al.
Applied and environmental microbiology, 67(10), 4603-4609 (2001-09-26)
We have identified in Pseudomonas aeruginosa strain JB2 a novel cluster of mobile genes encoding degradation of hydroxy- and halo-aromatic compounds. Nineteen open reading frames were located and, based on sequence similarities, were putatively identified as encoding a ring hydroxylating
A S Yuroff et al.
Applied and environmental microbiology, 69(12), 7401-7408 (2003-12-09)
We investigated the mechanisms of uptake of 2-chlorobenzoate (2-CBa) and 2-hydroxybenzoate (2-HBa) by Pseudomonas huttiensis strain D1. Uptake was monitored by assaying intracellular accumulation of 2-[UL-ring-14C]CBa and 2-[UL-ring-14C]HBa. Uptake of 2-CBa showed substrate saturation kinetics with an apparent Km of
W J Hickey et al.
Applied and environmental microbiology, 67(12), 5648-5655 (2001-11-28)
Protein mass spectrometry and molecular cloning techniques were used to identify and characterize mobile o-halobenzoate oxygenase genes in Pseudomonas aeruginosa strain JB2 and Pseudomonas huttiensis strain D1. Proteins induced in strains JB2 and D1 by growth on 2-chlorobenzoate (2-CBa) were
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