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34390

Supelco

1-Naphthylamine

analytical standard

Synonym(s):

α-Naphthylamine, 1-Aminonaphthalene

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About This Item

Linear Formula:
C10H7NH2
CAS Number:
Molecular Weight:
143.19
Beilstein:
386133
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

301 °C (lit.)

mp

47-50 °C (lit.)

density

1.114 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

Nc1cccc2ccccc12

InChI

1S/C10H9N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,11H2

InChI key

RUFPHBVGCFYCNW-UHFFFAOYSA-N

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Application

1-Naphthylamine may be used as an analytical reference standard for the determination of the analyte in ambient air and airborne particulate matters, hair dye and henna, and environmental water samples by various chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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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.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 1A

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

314.6 °F - closed cup

Flash Point(C)

157 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Determination of aromatic amines in hair dye and henna samples by ion-pair extraction and gas chromatography-mass spectrometry.
Akyuz M
Journal of Pharmaceutical and Biomedical Analysis, 47(1), 68-80 (2008)
Determination of aromatic primary amines at μ g-1 level in environmental waters by gas chromatography-mass spectrometry involving N-allyl-N′ -arylthiourea formation and their on-line pyrolysis to aryl isothiocyanates.
Singh V, et al.
Journal of Chromatography A, 1010(2), 243-253 (2003)
Simultaneous determination of aliphatic and aromatic amines in ambient air and airborne particulate matters by gas chromatography-mass spectrometry.
Akyuz M.
Atmospheric Environment, 42(16), 3809-3819 (2008)
Yuta Matsuoka et al.
Free radical biology & medicine, 53(11), 2112-2118 (2012-10-03)
Ascorbic acid is a small-molecule reductant with multiple functions in vivo. Reducing ascorbic acid intake leads to a lack of hydroxylation of prolines and lysines, causing a looser triple helix and resulting in scurvy. Ascorbic acid also acts as an
Fengtao Chen et al.
Journal of hazardous materials, 227-228, 474-479 (2012-06-02)
1-Naphthylamine wastewater causes severe environmental pollution because of its acute toxicity and carcinogenicity in humans, which makes it difficult to reuse by conventional technologies. In this study, we report an investigation of the electrochemical catalytic oxidation of 1-naphthylamine in synthetic

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