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About This Item
Linear Formula:
CH3C6H3(NO2)OH
CAS Number:
Molecular Weight:
153.14
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
mp
93-98 °C (lit.)
SMILES string
Cc1cc(ccc1O)[N+]([O-])=O
InChI
1S/C7H7NO3/c1-5-4-6(8(10)11)2-3-7(5)9/h2-4,9H,1H3
InChI key
KDQPMQNHVQVVMR-UHFFFAOYSA-N
Related Categories
General description
2-Methyl-4-nitrophenol is a nitrophenol derivative. The study of its crystal structure reveals the molecule to be nearly planar. Its synthesis has been reported. FT-IR and FT-Raman spectra and molecular modeling of 2-methyl-4-nitrophenol have been analyzed. It is reported to be one of the compounds in diesel exhaust particles (DEP) that shows potential vasodilatation activity in rats. Its reduction catalyzed by porous carbon-encapsulated gold nanoparticles has been investigated.
Application
2-Methyl-4-nitrophenol is suitable as a target compound in the study on measurement of methylnitrophenol concentrations and stable isotope ratios in the atmospheric particulate matter and as an internal standard in the determination of monoaromatic nitro compounds in atmospheric aerosols using high performance liquid chromatography electrospray tandem mass spectrometry (HPLC/ESI-MS/MS) method.
It may be used as starting material in the synthesis of 2-bromo-4-nitro-6-methylphenol.
It may be used as starting material in the synthesis of 2-bromo-4-nitro-6-methylphenol.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Jinrui Guo et al.
Chemical communications (Cambridge, England), 48(90), 11094-11096 (2012-10-11)
Gold nanoparticles encapsulated in porous carbon spheres with high surface areas (~800 m(2) g(-1)) have been synthesized by ultrasonic spray pyrolysis (USP). The porous carbon-encapsulated gold nanoparticles exhibit excellent catalytic activity toward the reductions of both hydrophilic and hydrophobic nitroaromatics.
2-Methyl-4-nitrophenol.
Bi S, et al.
Acta Crystallographica Section E, Structure Reports Online, 65(6), 1378-1378 (2009)
Nitration of substituted phenols by metal salts impregnated Yb-Mo-Montmorillonite KSF.
Yin WP and Shi M.
ARKIVOC (Gainesville, FL, United States), 6, 16-16 (2009)
Method for determination of stable carbon isotope ratio of methylnitrophenols in atmospheric particulate matter.
Moukhtar S, et al.
Atmospheric Measurement Techniques, 4(11), 2453-2464 (2011)
Inhibition of Photosynthesis by 4-Nitro-6-alkyl-phenols: Structure-Activity Studies in Wild Type and Five Mutants of Chlamydomonas reinhardtii Thylakoids.
Draber W, et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 48, 213-213 (1993)
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