Bis(hexamethylene)triamine - ≥95%(T) , CAS No.143-23-7

CAS: 143-23-7 Cat. No.: B152234 Fórmula: C₁₂H₂₉N₃ Peso molecular: 215.39 Beilstein Registry Number: 2323520 Número EC: 205-593-1

GRADE & PURITY ≥95%(T)

Synonyms

Bis(6-aminohexyl)amine | EINECS 205-593-1 | NSC 92231 | 1, N-(6-aminohexyl)- | Bishexamethylenetriamine | NSC92231 | NSC-92231 | UNII-BID902UF5V | 1,13-Diamino-7-azatridecane | AKOS015895016 | Dihexylenetriamine | Q27095431 | B1814 | Bis(hexamethylene)tri

Storage

Argon charged

Shipped In

Normal

Specifications

Sinónimos

Bis(6-aminohexyl)amine | EINECS 205-593-1 | NSC 92231 | 1, N-(6-aminohexyl)- | Bishexamethylenetriamine | NSC92231 | NSC-92231 | UNII-BID902UF5V | 1,13-Diamino-7-azatridecane | AKOS015895016 | Dihexylenetriamine | Q27095431 | B1814 | Bis(hexamethylene)tri

Especificaciones y pureza

≥95%(T)

Condiciones de almacenamiento de almacenamiento

Argon charged

Enviado en

Normal

Pureza

≥95%(T)

Nombres e identificadores

• Pubchem Sid: 508812715
• Sonrisas canónicas: C(CCCNCCCCCCN)CCN
• IUPAC Name: N'-(6-aminohexyl)hexane-1,6-diamine
• InChIKey: MRNZSTMRDWRNNR-UHFFFAOYSA-N
• INCHI: 1S/C12H29N3/c13-9-5-1-3-7-11-15-12-8-4-2-6-10-14/h15H,1-14H2
• Isómeros SMILES: C(CCCNCCCCCCN)CCN
• WGK Alemania: 1
• RTECS: MO1186250
• Número ONU: 3267
• Grupo de embalaje: I
• Peso molecular: 215.39
• Beilstein: 2323520
• Reaxy-Rn: 2323517
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2323517&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 Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary aliphatic amine - 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

Objetivos asociados (no humanos)

Dhps Deoxyhypusine synthase (51 Activities)

Discover Target: Dhps

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in Methanol
• Sensibilidad: Moisture sensitive
• Índice de refracción: 1.49
• Punto de inflamación (°F): 235.4 °F
• Punto de inflamación (°C): 113 °C
• Punto de ebullición (°C): 164°C/4mmHg(lit.)
• Punto de fusión (°C): 35 °C
• Peso molecular: 215.380 g/mol
• XLogP3: 0.800
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 12
• Exact Mass: 215.236 Da
• Monoisotopic Mass: 215.236 Da
• Topological Polar Surface Area: 64.099 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 95.000
• 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. Zihao Zhang, Siyu Yao, Changxue Wang, Miaomiao Liu, Feng Zhang, Xiaobing Hu, Hao Chen, Xin Gou, Kequan Chen, Yimei Zhu, Xiuyang Lu, Pingkai Ouyang, Jie Fu.  (2019)  CuZnCoOx multifunctional catalyst for in situ hydrogenation of 5-hydroxymethylfurfural with ethanol as hydrogen carrier.  JOURNAL OF CATALYSIS,      [PMID:] [10.1016/j.jcat.2019.04.011]

2. Ting Wu, Xiang Zhang, Hongju Liang, Quan Wang, Chun-Ling Liu, Wen-Sheng Dong.  (2025)  Tailored Co/SBA-15 catalyst for highly efficient hydrodeoxygenation of 5-hydroxymethylfurfural to 2,5-dimethylfuran.  APPLIED CATALYSIS A-GENERAL,      [PMID:] [10.1016/j.apcata.2025.120134]