1,2-Propanedithiol

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| ImageFile = 1,2-propanedithiol.png

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| 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

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| StdInChIKey = YGKHJWTVMIMEPQ-UHFFFAOYSA-N

| CASNo_Ref = {{cascite|correct|CAS}}

| CASNo = 814-67-5

| EINECS =

| PubChem = 61217

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| 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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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