Ethyltripropylammonium Iodide - ≥99%(T) , CAS No.15066-80-5

CAS: 15066-80-5 Cat. No.: E156124 Peso molecular: 299.24 Número EC: 679-912-1 PubChem CID: 23500186

GRADE & PURITY ≥99%(T)

Synonyms

AKOS015833265 | N-Ethyl-N,N-dipropylpropan-1-aminium iodide | Ethyl tri-N-propylammonium iodide | E0191 | ethyltri-n-propylammonium iodide | ethyltripropylazanium iodide | AS-65792 | ETHYLTRI-N-PROPYLAMMONIUM IODID | SY108915 | SCHEMBL1679298 | FT-0752510

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

AKOS015833265 | N-Ethyl-N, N-dipropylpropan-1-aminium iodide | Ethyl tri-N-propylammonium iodide | E0191 | ethyltri-n-propylammonium iodide | ethyltripropylazanium iodide | AS-65792 | ETHYLTRI-N-PROPYLAMMONIUM IODID | SY108915 | SCHEMBL1679298 | FT-0752510

Especificaciones y pureza

≥99%(T)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥99%(T)

Nombres e identificadores

• Sonrisas canónicas: CCC[N+](CC)(CCC)CCC.[I-]
• IUPAC Name: ethyl(tripropyl)azanium;iodide
• InChIKey: ZLHWTGZMAWUUMD-UHFFFAOYSA-M
• INCHI: 1S/C11H26N.HI/c1-5-9-12(8-4,10-6-2)11-7-3;/h5-11H2,1-4H3;1H/q+1;/p-1
• Isómeros SMILES: CCC[N+](CC)(CCC)CCC.[I-]
• PubChem CID: 23500186
• Peso molecular: 299.24
• Reaxy-Rn: 3914078

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Quaternary ammonium salts

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Quaternary ammonium salts
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetraalkylammonium salts
• Alternative Parents: Organic iodide salts Hydrocarbon derivatives Amines Organic cations
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tetraalkylammonium salt - Hydrocarbon derivative - Organic iodide salt - Organic salt - Amine - Organic cation - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as tetraalkylammonium salts. These are organonitrogen compounds containing a quaternary ammonium substituted with four alkyl chains.
• 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

• Peso molecular: 299.240 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 7
• Exact Mass: 299.111 Da
• Monoisotopic Mass: 299.111 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 82.200
• 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: 2

XLogP3

Referencias

1. Ruiqing Zhang, Huidong Xie, Fu Wang, Qiyu Zhao, Lingyi Meng, Zuobin Tang, Binbin Su, Hu Liu.  (2024)  Near-Infrared and Cyan Dual-Band Emission Copper Iodide Based Halides with [Cu6I9]3− Cluster.  Laser & Photonics Reviews,      [PMID:] [10.1002/lpor.202400450]

2. Linyuan Lian, Daming Xiong, Jibin Zhang, Mochen Jia, Ying Liu, Zhuangzhuang Ma, Xu Chen, Yanbing Han, Yongtao Tian, Xinjian Li, Jianbing Zhang, Peng Zhang, Zhifeng Shi.  (2025)  Thermally-Induced Reversible Phase Transition and Luminescence Switching in 0D Hybrid Copper Halide Isomers for Anti-Counterfeiting and Thermo-Responsive Scintillators.  Laser & Photonics Reviews,      [PMID:] [10.1002/lpor.202501538]