1-Ethyl-4-methylpyridinium Bromide - ≥98% , CAS No.32353-49-4

CAS: 32353-49-4 Cat. No.: E303436 Peso molecular: 202.1 Número EC: 801-378-7

GRADE & PURITY ≥98%

Synonyms

AS-61800 | D90607 | 1-ethyl-4-methylpyridinium bromide | E1272 | 1-ethyl-4-methylpyridin-1-ium;bromide | SCHEMBL1502745 | MFCD18384825 | 1-Ethyl-4-methylpyridin-1-ium bromide | AKOS028109893 | DTXSID90559315 | 1-ethyl-4-methylpyridiniumbromide | Pyridiniu

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Specifications

Sinónimos

AS-61800 | D90607 | 1-ethyl-4-methylpyridinium bromide | E1272 | 1-ethyl-4-methylpyridin-1-ium;bromide | SCHEMBL1502745 | MFCD18384825 | 1-Ethyl-4-methylpyridin-1-ium bromide | AKOS028109893 | DTXSID90559315 | 1-ethyl-4-methylpyridiniumbromide | Pyridiniu

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged, Desiccated

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504767616
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504767616
• Sonrisas canónicas: CC[N+]1=CC=C(C=C1)C.[Br-]
• IUPAC Name: 1-ethyl-4-methylpyridin-1-ium;bromide
• InChIKey: YZBRZOWPIBQUEJ-UHFFFAOYSA-M
• INCHI: 1S/C8H12N.BrH/c1-3-9-6-4-8(2)5-7-9;/h4-7H,3H2,1-2H3;1H/q+1;/p-1
• Isómeros SMILES: CC[N+]1=CC=C(C=C1)C.[Br-]
• Peso molecular: 202.1
• Reaxy-Rn: 3573016
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3573016&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Pyridines and derivatives
      • Subclass Methylpyridines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Pyridines and derivatives
• Subclass: Methylpyridines
• Intermediate Tree Nodes: Not available
• Direct Parent: Methylpyridines
• Alternative Parents: Pyridinium derivatives Heteroaromatic compounds Azacyclic compounds Organonitrogen compounds Organic bromide salts Hydrocarbon derivatives Organic cations
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Methylpyridine - Pyridinium - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organic bromide salt - Organic salt - Organonitrogen compound - Organic cation - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as methylpyridines. These are organic compounds containing a pyridine ring substituted at one or more positions by a methyl group.
• 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

• Sensibilidad: Hygroscopic
• Punto de fusión (°C): 129°C
• Peso molecular: 202.090 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 201.015 Da
• Monoisotopic Mass: 201.015 Da
• Topological Polar Surface Area: 3.900 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 72.600
• 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. Hao Wang, Xintong Zhang, Zhencai Zhang, Yiwen Zhang, Zhao Yang, Wentao Zhang, Chunshan Li, Fei Xu.  (2025)  Quantum-Chemically Guided Insights on Ionic Liquid Catalysts for Biobased Polycarbonate Synthesis─Mechanistic Exploration and Cation-Functionalized Optimization.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.4c10922]