Diheptylamine - ≥98% , CAS No.2470-68-0

CAS: 2470-68-0 Cat. No.: D154751 Peso molecular: 213.41 Número EC: 679-968-7

GRADE & PURITY ≥98%

Synonyms

Q26841313 | N-HEPTYL-1-HEPTANAMINE | 1-Heptanamine, N-heptyl- | MFCD00027309 | NCGC00341246-01 | AB00982877-03 | Di-n-heptylamine | EN300-40587 | Diheptylamine | SCHEMBL36300 | AKOS005174422 | D2675 | 5E36MJ5OI8 | AI3-16572 | UNII-5E36MJ5OI8 | N,N-Dihepty

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice

Specifications

Sinónimos

Q26841313 | N-HEPTYL-1-HEPTANAMINE | 1-Heptanamine, N-heptyl- | MFCD00027309 | NCGC00341246-01 | AB00982877-03 | Di-n-heptylamine | EN300-40587 | Diheptylamine | SCHEMBL36300 | AKOS005174422 | D2675 | 5E36MJ5OI8 | AI3-16572 | UNII-5E36MJ5OI8 | N, N-Dihepty

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Protected from light, Argon charged

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%

Nombres e identificadores

• Sonrisas canónicas: CCCCCCCNCCCCCCC
• IUPAC Name: N-heptylheptan-1-amine
• InChIKey: NJWMENBYMFZACG-UHFFFAOYSA-N
• INCHI: 1S/C14H31N/c1-3-5-7-9-11-13-15-14-12-10-8-6-4-2/h15H,3-14H2,1-2H3
• Isómeros SMILES: CCCCCCCNCCCCCCC
• Peso molecular: 213.41
• Reaxy-Rn: 1700185
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1700185&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Amines
        • Level5 Secondary amines
          • Level6 Dialkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Secondary amines
• Direct Parent: Dialkylamines
• Alternative Parents: Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as dialkylamines. These are organic compounds containing a dialkylamine group, characterized by two alkyl groups bonded to the amino nitrogen.
• 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

Propiedades químicas y físicas

• Sensibilidad: light & Moisture & air sensitive
• Índice de refracción: 1.44
• Punto de inflamación (°C): 108 °C
• Punto de ebullición (°C): 148°C/15mmHg(lit.)
• Peso molecular: 213.400 g/mol
• XLogP3: 5.500
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 12
• Exact Mass: 213.246 Da
• Monoisotopic Mass: 213.246 Da
• Topological Polar Surface Area: 12.000 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 89.500
• 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. Jing Ma, Yaoyao Linghu, Kai Yuan, Rui Zhou, Hui Gao, Peihua Zhao, Shaohui Guo, Huiqi Wang, Yongping Qu, Chao Shen, Keyu Xie.  (2025)  The synergistic effect of triazine-N and secondary amine-N anchors iodine species with MXene composite cathode for stable aqueous Zn–I2 battery.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.168594]