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Sigma-Aldrich

2,5-Dichlorobenzoic acid

97%

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About This Item

Linear Formula:
Cl2C6H3CO2H
CAS Number:
50-79-3
Molecular Weight:
191.01
Beilstein:
973353
EC Number:
200-065-7
MDL number:
MFCD00002416
UNSPSC Code:
12352100
PubChem Substance ID:
24848693
NACRES:
NA.22

Assay

97%

form

solid

bp

301 °C (lit.)

mp

151-154 °C (lit.)

SMILES string

OC(=O)c1cc(Cl)ccc1Cl

InChI

1S/C7H4Cl2O2/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3H,(H,10,11)

InChI key

QVTQYSFCFOGITD-UHFFFAOYSA-N

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General description

2,5-Dichlorobenzoic acid is converted to 4-chlorocatechol by Pseudomonas sp. CPE2 strain.

Application

2,5-Dichlorobenzoic acid was used as calibration standard to investigate the gas-phase OH reaction products of biphenyl, monochlorobiphenyl and dichlorophenyl.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

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Gas-phase oxidation products of biphenyl and polychlorinated biphenyls.
Brubaker WW and Hites RA.
Environmental Science & Technology, 32(24), 3913-3918 (1998)
Catherine J Duckett et al.
Rapid communications in mass spectrometry : RCM, 16(4), 245-247 (2002-01-30)
The use of directly coupled high performance liquid chromatography/inductively coupled plasma mass spectroscopy (HPLC/ICPMS) employing chlorine ((35)Cl/(37)Cl) detection has been investigated with respect to the detection and quantitation of the drugs diclofenac and chlorpromazine. By integration of peak areas in
V L Romanov et al.
Mikrobiologiia, 62(5), 887-896 (1993-09-01)
The strain Pseudomonas aeruginosa 142 isolated from the utilising PSBs bacterial association was capable of growth on 2-chloro- and 2,4-dichlorobenzoates as sole carbon sources, but it did not utilize 3-Cl, 4-Cl, 3,5-diCl- and 2,6-dichlorobenzoates. P. aeruginosa 142 dehalogenated 2-Cl-, 2,4-diCl-
B J van der Woude et al.
Biodegradation, 6(1), 39-46 (1995-01-01)
From long-term chemostat experiments, variants of Pseudomonas aeruginosa JB2 were obtained which exhibited altered properties with respect to the metabolism of 2,5-dichlorobenzoic acid (2,5-DBA). Thus, unlike the original strain JB2-WT, strain JB2-var1 is able to grow in continuous culture on
S A Kozlovsky et al.
Folia microbiologica, 38(5), 371-375 (1993-01-01)
A strain of Pseudomonas stutzeri KS25 utilizing 2-chlorobenzoic and 2,5-dichlorobenzoic acids as the sole carbon and energy source was isolated from polychlorophenol-contaminated soil and sewage, using the method of enrichment cultures. This strain was also able to grow on 2-fluoro-
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