1,2-Propanedithiol
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| verifiedrevid = 477204606
| ImageFile = 1,2-propanedithiol.png
| ImageSize = 120px
| PIN = Propane-1,2-dithiol{{cite book | title = Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book) | publisher = The Royal Society of Chemistry | date = 2014 | location = Cambridge | page = 697 | doi = 10.1039/9781849733069-FP001 | isbn = 978-0-85404-182-4}}
| OtherNames = 1,2-Dimercaptopropane
|Section1={{Chembox Identifiers
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| ChemSpiderID = 55160
| InChIKey = YGKHJWTVMIMEPQ-UHFFFAOYAG
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| StdInChI = 1S/C3H8S2/c1-3(5)2-4/h3-5H,2H2,1H3
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = YGKHJWTVMIMEPQ-UHFFFAOYSA-N
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = 814-67-5
| EINECS =
| PubChem = 61217
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = GS64223D79
| SMILES = SCC(S)C
| InChI = 1/C3H8S2/c1-3(5)2-4/h3-5H,2H2,1H3
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|Section2={{Chembox Properties
| C=3 | H=8 | S=2
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| BoilingPtC = 152
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| Solubility = Insoluble
| SolubleOther = soluble
| Solvent = organic solvents
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|Section7={{Chembox Hazards
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1,2-Propanedithiol, sometimes called 1,2-dimercaptopropane, is a thiol with the formula HSCH{{sub|2}}CH(SH)CH{{sub|3}}. This colorless, intensely odorous liquid is the simplest chiral dithiol. Related dithiols include 1,2-ethanedithiol, 2,3-dimercapto-1-propanesulfonic acid, and 1,3-propanedithiol. It is generated by the addition of H{{sub|2}}S to the related episulfide, CH{{sub|3}}CHCH{{sub|2}}S.
Refractive index = 1.531-1.541
References
External links
- {{cite web |url= http://webbook.nist.gov/cgi/cbook.cgi?Name=1%2C2-Propanedithiol|title= 1,2-Propanedithiol|year= 2011|publisher= NIST|access-date= 15 November 2011}}
{{DEFAULTSORT:Propanedithiol, 1, 3-}}
Category:Foul-smelling chemicals
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