Triallylamine - ≥97% , CAS No.102-70-5

CAS: 102-70-5 Cat. No.: T107428 Molecular Weight: 137.22 Beilstein Registry Number: 4(4)1061 EC Number: 203-048-2 PubChem CID: 7617

GRADE & PURITY ≥97%

Synonyms

N,N-bis(prop-2-enyl)prop-2-en-1-amine | NSC32635 | NSC-32635 | Tris(2-propenyl)amine | NCGC00254578-01 | 2-Propen-1-amine, N,N-di-2-propen-1-yl- | AMY22241 | DTXCID506174 | Triallylamine [UN2610] [Flammable liquid] | UN2610 | J-000772 | N,N-bis(prop-2-en

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Specifications

Synonyms

N, N-bis(prop-2-enyl)prop-2-en-1-amine | NSC32635 | NSC-32635 | Tris(2-propenyl)amine | NCGC00254578-01 | 2-Propen-1-amine, N, N-di-2-propen-1-yl- | AMY22241 | DTXCID506174 | Triallylamine [UN2610] [Flammable liquid] | UN2610 | J-000772 | N, N-bis(prop-2-en

Specifications & Purity

≥97%

Storage

Room temperature, Argon charged

Shipped In

FedEx DG Service

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥97%

Names and Identifiers

• Pubchem Sid: 488180505
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488180505
• Canonical Smiles: C=CCN(CC=C)CC=C
• IUPAC Name: N,N-bis(prop-2-enyl)prop-2-en-1-amine
• InChIKey: VPYJNCGUESNPMV-UHFFFAOYSA-N
• INCHI: 1S/C9H15N/c1-4-7-10(8-5-2)9-6-3/h4-6H,1-3,7-9H2
• Isomeric SMILES: C=CCN(CC=C)CC=C
• WGK Germany: 3
• RTECS: XX5950000
• PubChem CID: 7617
• UN Number: 2610
• Packing Group: III
• Molecular Weight: 137.22
• Beilstein: 4(4)1061
• Reaxy-Rn: 1740881

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Amines
        • Level5 Tertiary amines
          • Level6 Trialkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Tertiary amines
• Direct Parent: Trialkylamines
• Alternative Parents: Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tertiary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as trialkylamines. These are organic compounds containing a trialkylamine group, characterized by exactly three 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

Chemical and Physical Properties

• Solubility: Not miscible or difficult to mix in water.
• Sensitivity: Air sensitive
• Specific Rotation[α]: 1.451
• Flash Point(°C): 39 °C
• Boil Point(°C): 156 °C
• Melt Point(°C): -70°C
• Molecular Weight: 137.220 g/mol
• XLogP3: 2.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 6
• Exact Mass: 137.12 Da
• Monoisotopic Mass: 137.12 Da
• Topological Polar Surface Area: 3.200 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 92.100
• 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

References

1. Zhenwei Zhang, Junkai Zhang, Yixing Zhao, Yanli Wan, Sen Li, Yingwen Tang, Tao Li, Tingfang Tian, Li Wang.  (2022)  Reviving aged CsPbBr3 quantum dots by triallylamine etching.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2022.155775]

2. Yue Sun, Yingpeng Gu, Yu Jiang.  (2021)  Adsorption behavior of a tri-functionalized imprinted resin with high selectivity for 5-sulfosalicylic acid: Batch experiments and DFT calculation.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:33548783] [10.1016/j.jhazmat.2021.125271]

3. Ting Xu, Xiaoting Yan, Ayue Kang, Longhua Yang, Xinhui Li, Yue Tian, Ruige Yang, Shangshang Qin, Yong Guo.  (2024)  Development of Membrane-Targeting Fluorescent 2-Phenyl-1H-phenanthro[9,10-d]imidazole-Antimicrobial Peptide Mimic Conjugates against Methicillin-Resistant Staphylococcus aureus.  JOURNAL OF MEDICINAL CHEMISTRY,      [PMID:38491982] [10.1021/acs.jmedchem.4c00436]

4. Wenting Lan, Yafei Xiao, Minghua Zhang, Siyu Luo, Yue Jiang, Minmin Fan, Ya Cao.  (2026)  Thin and Robust Template-Reinforced Anion Exchange Membranes for Fuel Cells, Oil-Water Separation, and Humidity-Responsive Applications.  Small,      [PMID:41677060] [10.1002/smll.202510074]