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Supelco

4-Nitroaniline

analytical standard

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Linear Formula:
O2NC6H4NH2
CAS Number:
100-01-6
Molecular Weight:
138.12
Beilstein:
508690
EC Number:
202-810-1
MDL number:
MFCD00007858
PubChem Substance ID:
329753822
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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
GHS06,GHS08

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

415.4 °F - closed cup

Flash Point(C)

213.0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

Certificates of Analysis (COA)

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T1503
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25G
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705578-5MG-PW

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MMYOMAG-74K-13

1000309185

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Amit Kumar Mandal et al.
Scientific reports, 10(1), 5286-5286 (2020-03-27)
Cellular and tissue imaging in the second near-infrared window (NIR-II, ~1000-1350 nm) is advantageous for in vivo studies because of low light extinction by biological constituents at these wavelengths. However, deep tissue imaging at the single molecule sensitivity has not been
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)
Krzysztof Iwaszczuk et al.
Optics express, 17(24), 21969-21976 (2009-12-10)
We present a new method for data acquisition in time-resolved terahertz spectroscopy experiments. Our approach is based on simultaneous collection of reference and differential THz scans. Both the optical THz generation beam and the pump beam are modulated at two
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
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
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