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

CAS: 624-89-5 Cat. No.: E140654 Formula: CH₃CH₂SCH₃ Molecular Weight: 76.16 Beilstein Registry Number: 1696871 EC Number: 210-868-4 PubChem CID: 12230

GRADE & PURITY ≥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

Overview

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.

Specifications

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(methy Show more

Specifications & Purity

≥96%(GC)

Storage

Room temperature

Shipped In

Normal

Purity

≥96%(GC)

Names and Identifiers

Pubchem Sid

508814869

Pubchem Sid Url

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

Canonical Smiles

CCSC

IUPAC Name

methylsulfanylethane

InChIKey

WXEHBUMAEPOYKP-UHFFFAOYSA-N

INCHI

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

Isomeric SMILES

CCSC

WGK Germany

3

PubChem CID

12230

Molecular Weight

76.16

Beilstein

1696871

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organosulfur compounds
• Class: 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
• Description: 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

Chemical and Physical Properties

• Solubility: Miscible with alcohols and oils. Immiscible with water.
• Refractive Index: 1.4392
• Flash Point(°F): 5 °F
• Flash Point(°C): -15 °C
• Boil Point(°C): 66-67℃
• Melt Point(°C): -106℃
• Molecular Weight: 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