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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock Ethyl Propyl Sulfide - ≥96%(GC) , CAS No.4110-50-3
Synonyms
Ethyl propyl sulfide | LS-13098 | SCHEMBL200623 | EINECS 223-890-4 | Sulfide, ethyl propyl | Q27259528 | 1-ethylsulfanylpropane | Ethyl n-propyl sulfide | Ethyl propyl sulphide | Propyl ethyl sulfide | NSC163319 | NSC-163319 | UNII-4FK48S87VH | NSC 163319
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Why this grade ≥96%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonymes
Ethyl propyl sulfide | LS-13098 | SCHEMBL200623 | EINECS 223-890-4 | Sulfide, ethyl propyl | Q27259528 | 1-ethylsulfanylpropane | Ethyl n-propyl sulfide | Ethyl propyl sulphide | Propyl ethyl sulfide | NSC163319 | NSC-163319 | UNII-4FK48S87VH | NSC 163319
Spécifications et pureté
≥96%(GC)
Conditions de stockage de stockage
Room temperature
Noms et identifiants Pubchem Sid 508811793 Sourires canoniques CCCSCC IUPAC Name 1-ethylsulfanylpropane InChIKey ZDDDFDQTSXYYSE-UHFFFAOYSA-N INCHI 1S/C5H12S/c1-3-5-6-4-2/h3-5H2,1-2H3 Isomères SMILES CCCSCC Poids moléculaire 104.21 Beilstein 1(4)1451 Reaxy-Rn 1730935 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1730935&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification 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 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.
Structure 3D Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Point d'éclair (°C) 19 °C Point d'ébullition (°C) 117 °C Poids moléculaire 104.220 g/mol XLogP3 2.100 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 3 Exact Mass 104.066 Da Monoisotopic Mass 104.066 Da Topological Polar Surface Area 25.300 Ų Heavy Atom Count 6 Formal Charge 0 Complexity 19.900 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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