β-Naphthylamine - ≥98%, used for 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. various appli

CAS: 91-59-8 Cat. No.: N140874 Formule: C₁₀H₉N Poids moléculaire: 143.19 Beilstein Registry Number: 3939429 Numéro CE: 202-080-4

QUALITÉ & PURETÉ ≥98%

Synonyms

2-Naphthylamin|2-Naphtylamine|2-Aminonaftalen [Czech]|RCRA waste number U168|2-Naphthylamin [German]|2-NAPHTHYLAMINE|Naphthalen-2-ylamine|2-Naftylamin [Czech]|a-Naphthylamine|.beta.-Naphthylamin|6-Naphthylamine|beta-amino-naphthalene|Fast Scarlet Base B|2-Naphthalamine|ACETICACID-D|2-Naftylamin|2-NAPHTHYLAMINE [HSDB]|beta-Naphthylamine [UN1650] [Poison]|2-Aminonaftalen|2-NAPHTHYLAMINE [MI]|2-NAPHTHYLAMINE [IARC]|beta-Naftalamin|.beta.-Naftilamina|naphthalen-2-amine|beta-Naphthylamin|2-Aminonaphthalene|2-Amino-naphthalene|2-naphthyl amine|beta-Naftyloamina [Polish]|.beta.-naftyloamina|.beta.-Naphthylamine|2-naphthaleneamine|2-aminonaphthylamine|beta-Naphthylamin [German]|BNA|2-aminonapthalene|2-Naphthylamine mustard|2-naftilamina|beta-Naftalamin [Czech]|beta-Naftylamin [Czech]|USAF CB-22|.beta.-Naftylamin|2-Naphthylamine, powder|RCRA waste no. U168|.beta.-Naftalamin|2-Naftylamine|2-napthylamine|2-Naphthalenamine|beta-Naphthylamine|beta-Naftylamin|napthylamine|.BETA.-AMINONAPHTHALENE|2-Naftylamine [Dutch]

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice,FedEx DG Service

Vue d’ensemble

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

Spécifications

Synonymes

2-Naphthylamin | 2-Naphtylamine | 2-Aminonaftalen [Czech] | RCRA waste number U168 | 2-Naphthylamin [German] | 2-NAPHTHYLAMINE | Naphthalen-2-ylamine | 2-Naftylamin [Czech] | a-Naphthylamine | .beta.-Naphthylamin | 6-Naphthylamine | beta-amino-naphthalene | Fast Scarlet Base B | 2-Naphthalamine | ACETICACID-D | 2-Naftylamin | 2-NAPHTHYLAM Afficher plus

Spécifications et pureté

≥98%

Mécanismes biochimiques et physiologiques

Environmental carcinogen; induces bladder cancer.

Application

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.

Conditions de stockage de stockage

Store at 2-8°C,Protected from light

Expédié en

Wet ice,FedEx DG Service

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Pureté

≥98%

Noms et identifiants

Pubchem Sid

504751238

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504751238

Sourires canoniques

C1=CC=C2C=C(C=CC2=C1)N

IUPAC Name

naphthalen-2-amine

InChIKey

JBIJLHTVPXGSAM-UHFFFAOYSA-N

INCHI

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

Isomères SMILES

C1=CC=C2C=C(C=CC2=C1)N

WGK Allemagne

3

RTECS

QM2100000

Numéro ONU

1650(solid)3411(solution)

Groupe d'emballage

II

Poids moléculaire

143.19

Beilstein

3939429

Reaxy-Rn

606264

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=606264&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Naphthalenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Naphthalenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Naphthalenes
• Alternative Parents: Primary amines Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Naphthalene - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic homopolycyclic compound
• Description: This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings.
• External Descriptors: naphthylamine

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Soluble in Ethyl Acetate and Methanol
• Sensibilité: light sensitive
• Point d'ébullition (°C): 306°C
• Point de fusion (°C): 111-113°C
• Poids moléculaire: 143.180 g/mol
• XLogP3: 2.300
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 143.073 Da
• Monoisotopic Mass: 143.073 Da
• Topological Polar Surface Area: 26.000 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 133.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1