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31568

Supelco

4-Nitrotoluene

PESTANAL®, analytical standard

Synonyme(s) :

1-Methyl-4-nitrobenzene

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About This Item

Formule linéaire :
CH3C6H4NO2
Numéro CAS:
Poids moléculaire :
137.14
Numéro Beilstein :
1906911
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :

Qualité

analytical standard

Densité de vapeur

4.7 (vs air)

Pression de vapeur

5 mmHg ( 85 °C)

Gamme de produits

PESTANAL®

Température d'inflammation spontanée

734 °F

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Point d'ébullition

238 °C (lit.)

Pf

52-54 °C (lit.)

Densité

1.392 g/mL at 25 °C (lit.)

Application(s)

environmental

Format

neat

Chaîne SMILES 

Cc1ccc(cc1)[N+]([O-])=O

InChI

1S/C7H7NO2/c1-6-2-4-7(5-3-6)8(9)10/h2-5H,1H3

Clé InChI

ZPTVNYMJQHSSEA-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Informations légales

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogrammes

Skull and crossbonesHealth hazardEnvironment

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - STOT RE 2

Code de la classe de stockage

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

222.8 °F - closed cup

Point d'éclair (°C)

106.00 °C - closed cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Certificats d'analyse (COA)

Lot/Batch Number

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Consulter la Bibliothèque de documents

Avi Cagan et al.
The Analyst, 133(5), 585-587 (2008-04-23)
A highly selective and rapid electrochemical assay of the improvised explosive urea nitrate (UN) is reported. The method involves a short ( approximately 10 s) acid-catalyzed reaction of UN with 4-nitrotoluene (NT) followed by a rapid ( approximately 2 s)
S Ramalingam et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 75(4), 1308-1314 (2010-02-06)
In this work, the experimental and theoretical study on molecular structure and vibrational spectra of 4-nitrotoluene are studied. The FTIR and FTRaman experimental spectra of the molecule have been recorded in the range of 4000-100 cm(-1). Making use of the
Patricia Guerra et al.
Journal of separation science, 31(15), 2891-2898 (2008-07-31)
Ion mobility spectrometry (IMS) is routinely used in screening checkpoints for the detection of explosives and illicit drugs but it mainly relies on the capture of particles on a swab surface for the detection. Solid phase microextraction (SPME) has been
Baoliang Chen et al.
Bioresource technology, 102(2), 716-723 (2010-09-25)
Biochar derived from agricultural biomass waste is increasingly recognized as a multifunctional material for agricultural and environmental applications. Three novel magnetic biochars (MOP250, MOP400, MOP700) were prepared by chemical co-precipitation of Fe3+/Fe2+ on orange peel powder and subsequently pyrolyzing under
Muhammet Erkan Kose et al.
The journal of physical chemistry. B, 110(29), 14032-14034 (2006-07-21)
The photoluminescence from functionalized single-walled carbon nanotubes was found to be highly sensitive to the presence of nitroaromatic compounds such as nitrobenzene, 4-nitrotoluene, and 2,4-dinitrotoluene. The strong luminescence quenching in solution was at the upper limit of diffusion-control and also

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