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361127

Sigma-Aldrich

4-Chloro-3-nitrophenol

98%

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About This Item

Linear Formula:
ClC6H3(NO2)OH
CAS Number:
Molecular Weight:
173.55
Beilstein/REAXYS Number:
2094546
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

mp

125-128 °C (lit.)

functional group

chloro
nitro

SMILES string

Oc1ccc(Cl)c(c1)[N+]([O-])=O

InChI

1S/C6H4ClNO3/c7-5-2-1-4(9)3-6(5)8(10)11/h1-3,9H

InChI key

JUIKCULGDIZNDI-UHFFFAOYSA-N

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General description

4-Chloro-3-nitrophenol is a chloronitrophenol, widely used as an important building block for the synthesis of dyes, drugs, explosives and pesticides. Degradation of 4-chloro-3-nitrophenol by Pseudomonas sp. JHN is reported.

Application

4-Chloro-3-nitrophenol may be used as sole carbon and energy supplement for Pseudomonas sp. JHN.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Janmejay Pandey et al.
Applied microbiology and biotechnology, 92(3), 597-607 (2011-06-01)
Burkholderia sp. strain SJ98 (DSM 23195) was previously isolated and characterized for degradation and co-metabolic transformation of a number nitroaromatic compounds. In the present study, we evaluated its metabolic activity on chlorinated nitroaromatic compounds (CNACs). Results obtained during this study
Pankaj Kumar Arora et al.
Scientific reports, 4, 4475-4475 (2014-03-29)
A 4-chloro-3-nitrophenol (4C3NP)-mineralizing bacterium, Pseudomonas sp. JHN was isolated from a waste water sample collected from a chemically-contaminated area, India by an enrichment method. Pseudomonas sp. JHN utilized 4C3NP as a sole carbon and energy source and degraded it with
Surendra Vikram et al.
PloS one, 8(12), e84766-e84766 (2014-01-01)
Biodegradation of para-Nitrophenol (PNP) proceeds via two distinct pathways, having 1,2,3-benzenetriol (BT) and hydroquinone (HQ) as their respective terminal aromatic intermediates. Genes involved in these pathways have already been studied in different PNP degrading bacteria. Burkholderia sp. strain SJ98 degrades

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