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25580

Sigma-Aldrich

4-Chloro-2-nitrophenol

≥97.0%

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About This Item

Formula condensata:
ClC6H3(NO2)OH
Numero CAS:
89-64-5
Peso molecolare:
173.55
Beilstein:
2048031
Numero CE:
201-927-5
Numero MDL:
MFCD00007113
Codice UNSPSC:
12352100
ID PubChem:
57648134
NACRES:
NA.22

Livello qualitativo

100

Saggio

≥97.0%

Forma fisica

solid

Impurezze

~5% water

Punto di fusione

85-87 °C (lit.)
85-89 °C

Solubilità

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

Gruppo funzionale

chloro
nitro

Stringa SMILE

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

InChI

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

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Descrizione generale

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.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
053135/1
053135/1V
053135/1
53135/1

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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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