Ethyltrimethylammonium Iodide - ≥98% , CAS No.51-93-4

CAS: 51-93-4 Cat. No.: E156357 Peso molecular: 215.08 Número EC: 200-131-5 PubChem CID: 66125

GRADE & PURITY ≥98%

Synonyms

Ethanaminium, N,N,N-trimethyl-, iodide (1:1) | ethyl(trimethyl)azanium;iodide | CHEBI:55320 | ethyltrimethylazanium iodide | Ethanaminium, N,N,N-trimethyl-, iodide | Q27124226 | Ammonium, ethyltrimethyl-, iodide | EINECS 200-131-5 | MFCD00054229 | NSC1769

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

Ethanaminium, N, N, N-trimethyl-, iodide (1:1) | ethyl(trimethyl)azanium;iodide | CHEBI:55320 | ethyltrimethylazanium iodide | Ethanaminium, N, N, N-trimethyl-, iodide | Q27124226 | Ammonium, ethyltrimethyl-, iodide | EINECS 200-131-5 | MFCD00054229 | NSC1769

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488183739
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488183739
• Sonrisas canónicas: CC[N+](C)(C)C.[I-]
• IUPAC Name: ethyl(trimethyl)azanium;iodide
• InChIKey: ZPEBBUBSCOELHI-UHFFFAOYSA-M
• INCHI: 1S/C5H14N.HI/c1-5-6(2,3)4;/h5H2,1-4H3;1H/q+1;/p-1
• Isómeros SMILES: CC[N+](C)(C)C.[I-]
• RTECS: BQ6045000
• PubChem CID: 66125
• Peso molecular: 215.08
• Reaxy-Rn: 3911187

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: Organopnictogen compounds Organic iodide salts Hydrocarbon derivatives Amines
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tetraalkylammonium salt - Organopnictogen compound - Hydrocarbon derivative - Organic iodide salt - Organic salt - Amine - 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: quaternary ammonium salt - iodide salt

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 Sensitive
• Peso molecular: 215.080 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 215.017 Da
• Monoisotopic Mass: 215.017 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 33.700
• 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. Jinyun Peng, Qing Huang, Wenfeng Zhuge, Yuxia Liu, Cuizong Zhang, Wei Yang, Gang Xiang.  (2018)  Blue-light photoelectrochemical sensor based on nickel tetra-amined phthalocyanine-graphene oxide covalent compound for ultrasensitive detection of erythromycin.  BIOSENSORS & BIOELECTRONICS,      [PMID:29428591] [10.1016/j.bios.2018.02.009]

2. Jian Ao, Lingjun Bu, Yangtao Wu, Jinming Luo, Shiqing Zhou.  (2025)  Highly Selective Removal of Perchlorate from Water: Roles of Unconventional Hydrogen Bond and Hydrophobic Cavity.  Engineering,      [PMID:] [10.1016/j.eng.2024.12.029]