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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Allyl Propyl Sulfide - ≥97%(GC) , CAS No.27817-67-0
Synonyms
SCHEMBL3506130 | 3-(Propylthio)propene | MFCD00015220 | Q27263145 | AKOS006228764 | allyl(propyl)sulfane | Allyl n-propyl sulphide | ALLYLN-PROPYLSULFIDE | 3096O7WP53 | F13976 | PR 047 | 3-(propylsulfanyl)-1-propene | UNII-6038AN0CTJ | Allylpropyl sulfide
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Why this grade ≥97%(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 Sinónimos
SCHEMBL3506130 | 3-(Propylthio)propene | MFCD00015220 | Q27263145 | AKOS006228764 | allyl(propyl)sulfane | Allyl n-propyl sulphide | ALLYLN-PROPYLSULFIDE | 3096O7WP53 | F13976 | PR 047 | 3-(propylsulfanyl)-1-propene | UNII-6038AN0CTJ | Allylpropyl sulfide
Especificaciones y pureza
≥97%(GC)
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Sonrisas canónicas CCCSCC=C IUPAC Name 1-prop-2-enylsulfanylpropane InChIKey JMLIYQJQKZYHDQ-UHFFFAOYSA-N INCHI 1S/C6H12S/c1-3-5-7-6-4-2/h3H,1,4-6H2,2H3 Isómeros SMILES CCCSCC=C Peso molecular 116.22 Beilstein 1(3)1889 Reaxy-Rn 1739379 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1739379&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 Clase Allyl sulfur compounds Subclass Not available Intermediate Tree Nodes Not available Direct Parent Allyl sulfur compounds Alternative Parents Sulfenyl compounds Dialkylthioethers Hydrocarbon derivatives Molecular Framework Aliphatic acyclic compounds Substituents Allyl sulfur compound - Dialkylthioether - Sulfenyl compound - Thioether - Hydrocarbon derivative - Aliphatic acyclic compound Descripción This compound belongs to the class of organic compounds known as allyl sulfur compounds. These are compounds containing an allylsulfur group, with the general structure H2C(=CH2)CS. 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.
Estructura 3D Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Índice de refracción 1.47 Punto de inflamación (°C) 30 °C Punto de ebullición (°C) 140 °C Peso molecular 116.230 g/mol XLogP3 2.400 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 4 Exact Mass 116.066 Da Monoisotopic Mass 116.066 Da Topological Polar Surface Area 25.300 Ų Heavy Atom Count 7 Formal Charge 0 Complexity 41.400 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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