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25580

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
57648134
EC Number:
201-927-5
Beilstein/REAXYS Number:
2048031
MDL number:
MFCD00007113
Assay:
≥97.0%
Form:
solid

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

functional group

chloro, nitro

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

General description

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
AR053135/1
053135/1
53135/1

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Gajendra Kumar Pradhan et al.
ACS applied materials & interfaces, 4(2), 707-713 (2011-12-29)
A series of nanostructure zinc-iron mixed oxide photocatalysts have been fabricated by solution-combustion method using urea as the fuel, and nitrate salts of both iron and zinc as the metal source. Different characterization tools, such as X-ray diffraction (XRD), X-ray
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
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
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Global Trade Item Number

SKUGTIN
25580-250G04061832287126

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