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Merck
CN

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:
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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

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
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
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)
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
Samuel G Dennison et al.
Microbiological research, 165(8), 687-694 (2009-12-17)
Activated sludge from the Stickney Water Reclamation Plant of the Metropolitan Water Reclamation District of Greater Chicago was adapted in the laboratory to either benzoate or 2-chlorobenzoate as the sole carbon source in sequencing batch reactors with a 48-h feed-aerate-settle-draw

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