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· · COA & SDS 모든 제품에 대한 사용 가능 · 주식 상품에 대한 같은 날 배송 Ethyl methyl sulfide - ≥96%(GC) , CAS No.624-89-5
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
개요 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.
사양 동의어
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
이름과 식별자 Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508814869
IUPAC Name
methylsulfanylethane
InChIKey
WXEHBUMAEPOYKP-UHFFFAOYSA-N
INCHI
1S/C3H8S/c1-3-4-2/h3H2,1-2H3
고급 데이터 Taxonomic Classification Kingdom Organic compounds Superclass Organosulfur compounds 분류 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 설명 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.
3D 구조 인증서(CoA, COO, BSE/TSE 및 분석 차트) 화학 및 물리적 특성 용해성 Miscible with alcohols and oils. Immiscible with water. 굴절률 1.4392 발화점(°F) 5 °F 발화점(°C) -15 °C 끓는점(°C) 66-67℃ 녹는점(°C) -106℃ 분자량 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
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