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· · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino 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 Sinonimi
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
Specifiche e purezza
≥97%(GC)
Condizioni di conservazione di stoccaggio
Room temperature
Nomi e identificatori Pubchem Sid 508814639 Sorrisi canonici 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 Isomeri SMILES CCCSCC=C Peso molecolare 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=
Documentazione 📋 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 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 Descrizione 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.
Struttura 3D Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Indice di rifrazione 1.47 Punto di infiammabilità (°C) 30 °C Punto di ebollizione (°C) 140 °C Peso molecolare 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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