506877
2-Chlorobenzoic acid
PESTANAL®, analytical standard
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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
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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
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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)
B R Genthner
Biodegradation, 10(1), 27-33 (1999-07-29)
Dechlorination was the initial step of 2CB biodegradation in four 2-chlorobenzoate-degrading methanogenic consortia. Selected characteristics of ortho reductive dehalogenation were examined in consortia developed from the highest actively dechlorinating dilutions of the original 2CB consortia, designated consortia M34(-9), P20(-9), P21(-9)
Gang-hua Lang et al.
Applied microbiology and biotechnology, 83(6), 1085-1094 (2009-03-26)
TfdT is a LysR-type transcriptional regulator that activates the transcription of the chlorocatechol degradative gene operon tfdCDEF of the chlorobenzoate-degrading bacterium Burkholderia sp. NK8. To identify the amino acids involved in the effector recognition by TfdT, a polymerase-chain-reaction-based random mutagenesis
Satoshi Nishino et al.
The journal of physical chemistry. A, 111(30), 7041-7047 (2007-07-03)
Intramolecular hydrogen atom tunneling in 2-chlorobenzoic acid has been investigated by low-temperature matrix-isolation infrared spectroscopy with the aid of density functional theory calculation. Infrared spectra of two relatively stable syn isomers, SC and ST, were observed in argon and xenon
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
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