N,N-Dimethyl-1-naphthylamine - ≥98% , CAS No.86-56-6

CAS: 86-56-6 Cat. No.: N159179 Peso molecular: 171.24 Beilstein Registry Number: 12(3)2854 Número EC: 201-682-4

GRADE & PURITY ≥98%

Synonyms

N,N-Dimethyl-1-naftylamin | Z57169438 | D0755 | HY-D0222 | N,N-Dimethyl-1-naphthalenamine | N,N-DIMETHYL-1-NAPHTHYLAMINE [MI] | 1-(Dimethylamino)naphthalene | N,N-Dimethyl-1-naphthylamine, 99% | N,N-dimethylnaphthalen-1-amine | NCGC00188093-01 | A841719 |

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Sinónimos

N, N-Dimethyl-1-naftylamin | Z57169438 | D0755 | HY-D0222 | N, N-Dimethyl-1-naphthalenamine | N, N-DIMETHYL-1-NAPHTHYLAMINE [MI] | 1-(Dimethylamino)naphthalene | N, N-Dimethyl-1-naphthylamine, 99% | N, N-dimethylnaphthalen-1-amine | NCGC00188093-01 | A841719 |

Especificaciones y pureza

≥98%

Mecanismos bioquímicos y fisiológicos

N, N-Dimethyl-1-naphthylamine (1-Dimethylaminonaphthalene) is used to study nitrate reduction by organisms. Reduction of nitrate results in the formation of nitrite, which reacts with sulfanilic acid and 1-dimethylaminonaphthalene to form a red diazo dye.

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504751185
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751185
• Sonrisas canónicas: CN(C)C1=CC=CC2=CC=CC=C21
• IUPAC Name: N,N-dimethylnaphthalen-1-amine
• InChIKey: AJUXDFHPVZQOGF-UHFFFAOYSA-N
• INCHI: 1S/C12H13N/c1-13(2)12-9-5-7-10-6-3-4-8-11(10)12/h3-9H,1-2H3
• Isómeros SMILES: CN(C)C1=CC=CC2=CC=CC=C21
• RTECS: QM2825000
• Peso molecular: 171.24
• Beilstein: 12(3)2854
• Reaxy-Rn: 1424075
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1424075&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Naphthalenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Naphthalenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Naphthalenes
• Alternative Parents: Dialkylarylamines Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Naphthalene - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Tertiary amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aromatic homopolycyclic compound
• Descripción: 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: Not available

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Insoluble in water.
• Sensibilidad: light sensitive; air sensitive ;Moisture sensitive.
• Índice de refracción: 1.622
• Punto de inflamación (°F): 140°C
• Punto de inflamación (°C): 140°C
• Punto de ebullición (°C): 139-140 °C/13 mmHg
• Peso molecular: 171.240 g/mol
• XLogP3: 3.500
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 171.105 Da
• Monoisotopic Mass: 171.105 Da
• Topological Polar Surface Area: 3.200 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 165.000
• 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

Referencias

1. Le Ma, Yang Hou, Jun Nie, Xiaoqun Zhu.  (2025)  1-Naphthylamine thioxanthone-based one-component visible-light photoinitiators.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2025.109305]