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M62654

Sigma-Aldrich

3-Methyl-4-nitrophenol

98%

Sinonimo/i:

4-Nitro-m-cresol, 5-Hydroxy-2-nitrotoluene

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About This Item

Formula condensata:
CH3C6H3(NO2)OH
Numero CAS:
Peso molecolare:
153.14
Beilstein:
1868105
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:

Saggio

98%

Punto di fusione

125-130 °C (lit.)

Stringa SMILE

Cc1cc(O)ccc1[N+]([O-])=O

InChI

1S/C7H7NO3/c1-5-4-6(9)2-3-7(5)8(10)11/h2-4,9H,1H3
PIIZYNQECPTVEO-UHFFFAOYSA-N

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Pittogrammi

Exclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

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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T Galeano-Díaz et al.
Analytica chimica acta, 618(2), 131-139 (2008-06-03)
A method, using stripping square wave voltammetry (Ad-SSWV), for the simultaneous determination of fenitrothion (FEN) and its metabolites: fenitrooxon (OXON) and 3-methyl-4-nitrophenol (3-MET) in environmental samples is reported. All three compounds produce, at mercury electrode (HMDE), an electrochemical signal due
S M A D Zayed et al.
Chemosphere, 70(9), 1653-1659 (2007-09-08)
The decomposition of (14)C-fenitrothion on silica gel chromatoplates as well as in polar and non polar solvents under sunlight and ultraviolet light was investigated, Its stability to sunlight on leaf surfaces of bean plants and on different surfaces (such as
Chie Furuta et al.
Toxicology and applied pharmacology, 229(1), 109-120 (2008-03-14)
Studies of nitrophenols isolated from diesel exhaust particles (DEPs), 3-methyl-4-nitrophenol (PNMC) and 4-nitro-3-phenylphenol (PNMPP) have revealed that these chemicals possess estrogenic and anti-androgenic activity in vitro and in vivo and that PNMC accumulate in adrenal glands in vivo. However, the
Keiko Noguchi et al.
Biomedical chromatography : BMC, 21(11), 1135-1142 (2007-06-23)
Diesel exhaust particulate extract (DEPE) was obtained from diesel exhaust particulates with Soxhlet extraction using dichloromethane. After separating DEPE into 11 fractions by liquid-liquid extraction, the neutral fraction (N) showed anti-estrogenic activity and the weak acid (phenol) fraction (WA(P)) showed
ChunMei Li et al.
The Journal of reproduction and development, 53(3), 673-678 (2007-01-05)
In a previous study, we found that 3-methyl-4-nitrophenol (PNMC), a component of diesel exhaust particles and also a degradation product of the insecticide fenitrothion, exhibits reproductive toxicity in the adult male Japanese quail. The present study investigated the toxicity of

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