Tribenzylamine - ≥99% , CAS No.620-40-6

CAS: 620-40-6 Cat. No.: T162177 Peso molecular: 287.41 Beilstein Registry Number: 2214680 Número EC: 210-638-3 PubChem CID: 24321

GRADE & PURITY ≥99%

Synonyms

Tribenzylamine, >=99% | N,N-dibenzyl-1-phenylmethanamine | N,N-dibenzyl-1-phenyl-methanamine | MFCD00004773 | T0341 | N,N-Bis(phenylmethyl)benzenemethanamine | Benzenemethanamine, N,N-bis(phenylmethyl)- | (N,N-Dibenzylaminomethyl)benzene | DTXCID3027031 |

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

Tribenzylamine, >=99% | N, N-dibenzyl-1-phenylmethanamine | N, N-dibenzyl-1-phenyl-methanamine | MFCD00004773 | T0341 | N, N-Bis(phenylmethyl)benzenemethanamine | Benzenemethanamine, N, N-bis(phenylmethyl)- | (N, N-Dibenzylaminomethyl)benzene | DTXCID3027031 |

Especificaciones y pureza

≥99%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 488182876
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488182876
• Sonrisas canónicas: C1=CC=C(C=C1)CN(CC2=CC=CC=C2)CC3=CC=CC=C3
• IUPAC Name: N,N-dibenzyl-1-phenylmethanamine
• InChIKey: MXHTZQSKTCCMFG-UHFFFAOYSA-N
• INCHI: 1S/C21H21N/c1-4-10-19(11-5-1)16-22(17-20-12-6-2-7-13-20)18-21-14-8-3-9-15-21/h1-15H,16-18H2
• Isómeros SMILES: C1=CC=C(C=C1)CN(CC2=CC=CC=C2)CC3=CC=CC=C3
• WGK Alemania: 3
• PubChem CID: 24321
• Peso molecular: 287.41
• Beilstein: 2214680
• Reaxy-Rn: 2214682

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Phenylmethylamines

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Phenylmethylamines
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylmethylamines
• Alternative Parents: Benzylamines Aralkylamines Trialkylamines Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenylmethylamine - Benzylamine - Aralkylamine - Tertiary aliphatic amine - Tertiary amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenylmethylamines. These are compounds containing a phenylmethtylamine moiety, which consists of a phenyl group substituted by an methanamine.
• 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

• Solubilidad: Soluble in chloroform, benzene, toluene, ether
• Punto de inflamación (°F): 397°F
• Punto de inflamación (°C): 203°C
• Punto de ebullición (°C): 390°C
• Punto de fusión (°C): 91-94°C
• Peso molecular: 287.400 g/mol
• XLogP3: 4.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 6
• Exact Mass: 287.167 Da
• Monoisotopic Mass: 287.167 Da
• Topological Polar Surface Area: 3.200 Ų
• Heavy Atom Count: 22
• Formal Charge: 0
• Complexity: 235.000
• 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. Yanan Zhang, Zhenli Zhang, Hongjing Han, Mei Zhang, Haiying Wang, Hua Song, Yanguang Chen.  (2022)  Effective removal of organic dyes using the ultrasonic-assisted hydrothermal synthesis of NaP zeolite doping Cu or Fe in Fenton-like oxidation systems.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2022.121767]

2. Xinmeng Xu, Xiang Xu, Yanning Zeng, Faai Zhang.  (2021)  Oxygen-tolerant photo-induced metal-free atom transfer radical polymerization.  JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY,      [PMID:] [10.1016/j.jphotochem.2021.113191]

3. Zhe Zhang, Shengqiu Zhao, Yucong Liao, Yao Li, Bingxuan Liu, Zhengrui Xiao, Zeqi You, Tian Tian, Lan Zhang, Siew Hwa Chan, Haolin Tang.  (2025)  Side-chain sterically induced directional units construct stable and continuous ion transport channels for anion exchange membranes.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2025.124191]