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

CAS: 624-89-5 Cat. No.: E140654 分子式: CH₃CH₂SCH₃ 分子量: 76.16 Beilstein Registry Number: 1696871 EC番号: 210-868-4 PubChem CID: 12230

グレード＆純度 ≥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

概要

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.

仕様

同義語

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 もっと見る

仕様と純度

≥96%(GC)

保管条件

Room temperature

入荷

Normal

純度

≥96%(GC)

名前と識別子

パブケム・シド

508814869

パブケム・シド・ウル

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

カノニカル・スマイル

CCSC

IUPAC Name

methylsulfanylethane

InChIKey

WXEHBUMAEPOYKP-UHFFFAOYSA-N

INCHI

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

異性体SMILES

CCSC

WGKドイツ

3

PubChem CID

12230

分子量

76.16

Beilstein

1696871

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organosulfur compounds
• 分類: 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
• 説明: 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

化学的性質と物理的性質

• 溶解度: Miscible with alcohols and oils. Immiscible with water.
• 屈折率: 1.4392
• 引火点（°F）: 5 °F
• 引火点（°C）: -15 °C
• 沸点（°C）: 66-67℃
• 融点（°C）: -106℃
• 分子量: 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