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Supelco

1-Naphthylamine

analytical standard

Sinônimo(s):

α-Naphthylamine, 1-Aminonaphthalene

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About This Item

Fórmula linear:
C10H7NH2
Número CAS:
134-32-7
Peso molecular:
143.19
Beilstein:
386133
Número MDL:
MFCD00004016
Código UNSPSC:
12000000
ID de substância PubChem:
24867770

grau

analytical standard

embalagem

ampule of 250 mg

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

p.e.

301 °C (lit.)

pf

47-50 °C (lit.)

densidade

1.114 g/mL at 25 °C (lit.)

aplicação(ões)

cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

temperatura de armazenamento

room temp

cadeia de caracteres SMILES

Nc1cccc2ccccc12

InChI

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

chave InChI

RUFPHBVGCFYCNW-UHFFFAOYSA-N

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Aplicação

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

314.6 °F - closed cup

Ponto de fulgor (°C)

157 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
LC25139V
LC24371V
LC23257V
LC05035V
LB96738V

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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Arvydas Tamulis et al.
Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life, 43(1), 49-66 (2012-12-18)
The quantum mechanical self-assembly of two separate photoactive supramolecular systems with different photosynthetic centers was investigated by means of density functional theory methods. Quantum entangled energy transitions from one subsystem to the other and the assembly of logically controlled artificial
V Chubanov et al.
British journal of pharmacology, 166(4), 1357-1376 (2012-01-17)
Transient receptor potential cation channel subfamily M member 7 (TRPM7) is a bifunctional protein comprising a TRP ion channel segment linked to an α-type protein kinase domain. TRPM7 is essential for proliferation and cell growth. Up-regulation of TRPM7 function is
Xiaolin Zhang et al.
Inorganic chemistry, 51(4), 2325-2331 (2012-02-10)
A unique gadolinium complex, Nap-DO3A-Gd, comprising a naphthylamine luminescent moiety, a di-2-picolylamine (DPA) binding chelator, and a 1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid (DO3A) moiety has been designed and synthesized as a dual-functional probe for selective magnetic resonance imaging and fluorescent sensing of copper(II)
Todd M Doran et al.
Proteins, 80(4), 1053-1065 (2012-01-19)
Aromatic amino acids strongly promote cross-β amyloid formation; whether the amyloidogenicity of aromatic residues is due to high hydrophobicity and β-sheet propensity or formation of stabilizing π-π interactions has been debated. To clarify the role of aromatic residues on amyloid
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
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