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Merck
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31569

Supelco

4-nitroaniline

analytical standard

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About This Item

Formule linéaire :
O2NC6H4NH2
Numéro CAS:
Poids moléculaire :
138.12
Numéro Beilstein :
508690
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Pureté

≥98% (GC)

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Point d'ébullition

260 °C/100 mmHg (lit.)

Pf

146-149 °C (lit.)

Application(s)

environmental

Format

neat

Chaîne SMILES 

Nc1ccc(cc1)[N+]([O-])=O

InChI

1S/C6H6N2O2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H,7H2

Clé InChI

TYMLOMAKGOJONV-UHFFFAOYSA-N

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Description générale

4-Nitroaniline is an aromatic amine, used as an intermediate in the production of p-phenylenediamine, azo dyes, antioxidants, fuel additives, corrosion inhibitors and pesticides.

Application

4-Nitroaniline may be used as an analytical standard for the determination of 4-nitrophenol in water samples by competitive flow immunoassay coupled with a fluorescence detector.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Produit des réactions chromogènes

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictogrammes

Skull and crossbonesHealth hazard

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - 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)

415.4 °F - closed cup

Point d'éclair (°C)

213.0 °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

A kinetic study on the degradation of p-nitroaniline by Fenton oxidation process.
Sun JH, et al.
Journal of Hazardous Materials, 148(1-2), 172-177 (2007)
Competitive flow immunoassay with fluorescence detection for determination of 4-nitrophenol.
Nistor C, et al.
Analytica Chimica Acta, 426(2), 185-195 (2001)
Kumi Y Inoue et al.
Innate immunity, 18(2), 343-349 (2011-08-17)
Here, we report the development of an electrochemical detection method for endotoxin based on the Limulus amebocyte lysate (LAL) assay. A mixture of LAL reagent and endotoxin sample solution was incubated for 1 h. The endotoxin activated a cascade reaction
Patrick Hauske et al.
Bioorganic & medicinal chemistry, 17(7), 2920-2924 (2009-02-24)
Protein quality control factors are involved in many key physiological processes and severe human diseases that are based on misfolding or amyloid formation. Prokaryotic representatives are often virulence factors of pathogenic bacteria. Therefore, protein quality control factors represent a novel
Kunquan Li et al.
Journal of hazardous materials, 178(1-3), 553-559 (2010-03-06)
Activated carbon fibers (ACFs) were prepared for the removal of p-nitroaniline (PNA) from cotton stalk by chemical activation with NH(4)H(2)PO(4) and subsequent physical activation with steam. Surface properties of the prepared ACFs were performed using nitrogen adsorption, FTIR spectroscopy and

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