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31618

Supelco

2-Naphthylamine

analytical standard

Sinônimo(s):

β-Naphthylamine, 2-Aminonaphthalene

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About This Item

Fórmula linear:
C10H7NH2
Número CAS:
91-59-8
Peso molecular:
143.19
Beilstein:
3939429
Número CE:
202-080-4
Número MDL:
MFCD00004112
Código UNSPSC:
41116107
ID de substância PubChem:
329753849
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

pb

306 °C (lit.)

pf

111-113 °C (lit.)

densidade

1.061 g/mL at 25 °C (lit.)

aplicação(ões)

cleaning products
cosmetics
food and beverages
personal care

formato

neat

cadeia de caracteres SMILES

Nc1ccc2ccccc2c1

InChI

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

chave InChI

JBIJLHTVPXGSAM-UHFFFAOYSA-N

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Descrição geral

2-Naphthylamine is a carcinogenic aromatic amine which induces tumor in urinary bladder.

Aplicação

2-Naphthylamine has been used as reference standard during isolation and identification of urinary metabolites using preparative thin-layer chromatography and gas-liquid chromatography/mass spectral analysis.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Atenção

Restricted to professional users. Attention − Avoid exposure − obtain special instructions before use.

Palavra indicadora

Danger

Frases de perigo

H302,H350,H411

Classificações de perigo

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

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Equipamento de proteção individual

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Choose from one of the most recent versions:

Certificados de análise (COA)

Lot/Batch Number
BCCM3097
BCCL3096
BCCG4049
BCCC2053
BCBZ3240

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Metabolic conversion of 1-and 2-nitronaphthalene to 1-and 2-naphthylamine in the rat.
Johnson, Dale E., and Herbert H. Cornish.
Toxicology and Applied Pharmacology, 46.3, 549-553 (1978)
Formation of urothelial and hepatic DNA adducts from carcinogen 2-naphthylamine.
Kadlubar FF
Carcinogenesis, 2(5), 467-470 (1981)
Weimei Sun et al.
The Journal of pharmacology and experimental therapeutics, 375(3), 510-521 (2020-10-10)
Inhibition of the serine protease enteropeptidase (EP) opens a new avenue to the discovery of chemotherapeutics for the treatment of metabolic diseases. Camostat has been used clinically for treating chronic pancreatitis in Japan; however, the mechanistic basis of the observed
Dylan M Owen et al.
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Lipid microdomains are postulated to regulate many membrane-associated processes but have remained highly controversial. Here we provide the first direct evidence that the plasma membrane of intact, live cells is comprised of a sub-resolution mixture of approximately 76% ordered and
Carlos de la Haba et al.
Biochimica et biophysica acta, 1828(2), 357-364 (2012-09-04)
Plasma membrane is one of the preferential targets of reactive oxygen species which cause lipid peroxidation. This process modifies membrane properties such as membrane fluidity, a very important physical feature known to modulate membrane protein localization and function. The aim
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