Ethyl methyl sulfide - ≥96%(GC) , CAS No.624-89-5

CAS: 624-89-5 Cat. No.: E140654 Fórmula: CH₃CH₂SCH₃ Peso molecular: 76.16 Beilstein Registry Number: 1696871 Número CE: 210-868-4 PubChem CID: 12230

GRAU & PUREZA ≥96%(GC)

Synonyms

1-(methylthio)ethane|ethyl methyl thioether|(methylsulfanyl)ethane|Ethyl methyl sulfide|Ethane, (methylthio)-|Methyl ethyl sulphide|Sulfide, ethyl methyl|Methylthioethane|2-THIABUTANE|MeSEt|METHYL ETHYL SULFIDE [FHFI]|Methyl ethyl sulfide|(Methylthio)ethane|methylethyl sulfide|methylsulfanylethane|Ethyl(methyl)sulfane|1-(Methylsulfanyl)ethane

Storage

Room temperature

Shipped In

Normal

Visão geral

Product Application：

Ethyl Methyl Sulfide is used as a corrosion inhibitor for zinc metal which finds wide applications like electrode material in batteries, sacrificial anodes and metallic coatings. It is used in mixtures designed to odorize natural gas and is made to by-pass injection system.

Especificações

Sinónimos

1-(methylthio)ethane | ethyl methyl thioether | (methylsulfanyl)ethane | Ethyl methyl sulfide | Ethane, (methylthio)- | Methyl ethyl sulphide | Sulfide, ethyl methyl | Methylthioethane | 2-THIABUTANE | MeSEt | METHYL ETHYL SULFIDE [FHFI] | Methyl ethyl sulfide | (Methylthio)ethane | methylethyl sulfide | methylsulfanylethane | Ethyl(methy Show more

Especificações e pureza

≥96%(GC)

Condições de armazenamento de armazenamento

Room temperature

Enviado em

Normal

Pureza

≥96%(GC)

Nomes e identificadores

Pubchem Sid

508814869

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508814869

Sorrisos canónicos

CCSC

IUPAC Name

methylsulfanylethane

InChIKey

WXEHBUMAEPOYKP-UHFFFAOYSA-N

INCHI

1S/C3H8S/c1-3-4-2/h3H2,1-2H3

SMILES isoméricas

CCSC

WGK Alemanha

3

PubChem CID

12230

Peso molecular

76.16

Beilstein

1696871

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organosulfur compounds
    • Classe Thioethers
      • Subclass Dialkylthioethers

• Kingdom: Organic compounds
• Superclass: Organosulfur compounds
• Classe: Thioethers
• Subclass: Dialkylthioethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkylthioethers
• Alternative Parents: Sulfenyl compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dialkylthioether - Sulfenyl compound - Hydrocarbon derivative - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as dialkylthioethers. These are organosulfur compounds containing a thioether group that is substituted by two alkyl groups.
• 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

Propriedades químicas e físicas

• Solubilidade: Miscible with alcohols and oils. Immiscible with water.
• Índice de refração: 1.4392
• Ponto de inflamação (°F): 5 °F
• Ponto de inflamação (°C): -15 °C
• Ponto de ebulição (°C): 66-67℃
• Ponto de fusão (°C): -106℃
• Peso molecular: 76.160 g/mol
• XLogP3: 1.500
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 76.0347 Da
• Monoisotopic Mass: 76.0347 Da
• Topological Polar Surface Area: 25.300 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 7.200
• 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: 1