422908
2-Methyl-4-nitrophenol
97%
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About This Item
Formula condensata:
CH3C6H3(NO2)OH
Numero CAS:
Peso molecolare:
153.14
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
97%
Punto di fusione
93-98 °C (lit.)
Gruppo funzionale
nitro
Stringa SMILE
Cc1cc(ccc1O)[N+]([O-])=O
InChI
1S/C7H7NO3/c1-5-4-6(8(10)11)2-3-7(5)9/h2-4,9H,1H3
KDQPMQNHVQVVMR-UHFFFAOYSA-N
Categorie correlate
Descrizione generale
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.
Applicazioni
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.
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
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
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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A Sechman et al.
Domestic animal endocrinology, 70, 106378-106378 (2019-09-13)
To assess the effects of 4-nitrophenol (PNP) and 3-methyl-4-nitrophenol (PNMC) on steroidogenesis in the chicken ovary, white (WF, 1-4 mm) and yellowish (YF, 4-8 mm) prehierarchical follicles were incubated in a medium supplemented with PNP or PNMC (10-8-10-4 M), ovine LH (oLH; 10 ng/mL)
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)
Yoki Mori et al.
Biological & pharmaceutical bulletin, 26(3), 394-395 (2003-03-04)
The compounds in diesel exhaust particles (DEP) that are responsible for vasodilatation were isolated and characterized for the first time. From benzene extract of DEP, 2-methyl-4-nitrophenol, 3-methyl-4-nitrophenl and 4-nitrophenol were isolated, and their vasodilatation activities were confirmed. 3-methyl-4-nitrophenol caused dilatation
Zoran Kitanovski et al.
Journal of chromatography. A, 1268, 35-43 (2012-11-06)
Nitrogen-containing organic compounds in the atmosphere have drawn attention owing to their impact on aerosol chemistry and physics and their potential adverse effects on the biosphere. Among them, nitrocatechols and their homologs have recently been associated with biomass burning. In
2-Methyl-4-nitrophenol.
Bi S, et al.
Acta Crystallographica Section E, Structure Reports Online, 65(6), 1378-1378 (2009)
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