506877
2-氯苯甲酸
PESTANAL®, analytical standard
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线性分子式:
ClC6H4CO2H
化学文摘社编号:
分子量:
156.57
EC Number:
204-285-4
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
907340
MDL number:
InChI key
IKCLCGXPQILATA-UHFFFAOYSA-N
InChI
1S/C7H5ClO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,(H,9,10)
SMILES string
OC(=O)c1ccccc1Cl
grade
analytical standard
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
Quality Level
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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
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
343.4 °F
flash_point_c
173 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
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)
Meltem Urgun-Demirtas et al.
Water environment research : a research publication of the Water Environment Federation, 77(5), 511-518 (2005-11-09)
The feasibility of applying bacterial hemoglobin technology to degrade 2-chlorobenzoate (2-CBA) through co-metabolism under hypoxic conditions in a membrane bioreactor (MBR) process has been studied in the laboratory. 2-chlorobenzoate removal and chloride release rates in the MBR system varied from
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
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(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
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