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Supelco

4-Nitroaniline

analytical standard

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About This Item

Linear Formula:
O2NC6H4NH2
CAS Number:
Molecular Weight:
138.12
Beilstein/REAXYS Number:
508690
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

assay

≥98% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

260 °C/100 mmHg (lit.)

mp

146-149 °C (lit.)

application(s)

environmental

format

neat

SMILES string

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

InChI

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

InChI key

TYMLOMAKGOJONV-UHFFFAOYSA-N

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General description

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.
Product of chromogenic reactions.

Recommended products

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.

pictograms

Skull and crossbonesHealth hazard

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 3

flash_point_f

415.4 °F - closed cup

flash_point_c

213.0 °C - closed cup

ppe

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


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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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