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Sigma-Aldrich

4-Chloro-2-nitrophenol

≥97.0%

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About This Item

Linear Formula:
ClC6H3(NO2)OH
CAS Number:
89-64-5
Molecular Weight:
173.55
Beilstein:
2048031
EC Number:
201-927-5
MDL number:
MFCD00007113
UNSPSC Code:
12352100
PubChem Substance ID:
57648134
NACRES:
NA.22

Assay

≥97.0%

form

solid

impurities

~5% water

mp

85-87 °C (lit.)
85-89 °C

solubility

dioxane: soluble 0.5 g/5mL, clear, faintly yellow to yellow

SMILES string

Oc1ccc(Cl)cc1[N+]([O-])=O

InChI

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

InChI key

NWSIFTLPLKCTSX-UHFFFAOYSA-N

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General description

Adsorption of 4-chloro-2-nitrophenol onto single-walled and multi-walled carbon nanotubes has been studied. Biotransformation of 4-chloro-2-nitrophenol by Bacillus sp. strain MW-1 has been studied.

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)

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Ali Mehrizad et al.
Iranian journal of environmental health science & engineering, 9(1), 5-5 (2013-02-02)
The adsorption characteristics of 4-chloro-2-nitrophenol (4C2NP) onto single-walled and multi-walled carbon nanotubes (SWCNTs and MWCNTs) from aqueous solution were investigated with respect to the changes in the contact time, pH of solution, carbon nanotubes dosage and initial 4C2NP concentration. Experimental
Babita Sur et al.
The Science of the total environment, 426, 296-303 (2012-04-24)
Anionic 2-nitro-4-chlorophenol (NCP) may occur in surface waters as a nitroderivative of 4-chlorophenol, which is a transformation intermediate of the herbicide dichlorprop. Here we show that NCP would undergo efficient photochemical transformation in environmental waters, mainly by direct photolysis and
Ia V Voznyĭ et al.
Voprosy meditsinskoi khimii, 42(4), 348-354 (1996-10-01)
Synthesis of beta-maltosides, p-nitrophenyl-beta-D-maltoside and 4-methylumbelliferyl-beta-D-maltoside, based on interaction of hepta-acetate-beta-D-maltosyl fluoride with the corresponding trimethylsilyl ethers of p-nitrophenol and 4-methylumbelliferone is described. 2-Chloro-4-nitrophenyl-beta-D-maltoside was synthesized by interaction of hepta-acetate-alpha-D-maltosyl bromide with 2-chloro-4-nitrophenol in two phase system using phase transfer
D Sreekanth et al.
Journal of hazardous materials, 164(2-3), 1532-1539 (2008-11-07)
This Study describes the feasibility of anaerobic degradation of United States Environmental Protection Agency (USEPA) listed 4-chloro-2-nitrophenol (4C-2-NP), 2-chloro-4-nitrophenol (2C-4-NP), 2-chloro-5-methylphenol (2C-5-MP) from a simulated wastewater using four identical 7L bench scale hybrid up flow anaerobic sludge blankets (HUASBs) at
P Saritha et al.
Journal of hazardous materials, 149(3), 609-614 (2007-08-21)
In the present study an attempt is made efficiently to degrade USEPA listed 4-chloro-2-nitrophenol (4C-2-NP), widely available in bulk drug and pesticide wastes using various advanced oxidation processes (AOPs). A comparative assessment using various AOPs (UV, H(2)O(2,) UV/H(2)O(2), Fenton, UV/Fenton
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