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1,3-Propanedithiol, 97%

CAS: 109-80-8 | C3H8S2 | 108.217 g/mol

$48.15 - $377.62

Chemical Identifiers

CAS 109-80-8
Molecular Formula C3H8S2
Molecular Weight (g/mol) 108.217
MDL Number MFCD00004904
InChI Key ZJLMKPKYJBQJNH-UHFFFAOYSA-N
Synonym 1,3-propanedithiol, 1,3-dimercaptopropane, trimethylene dimercaptan, trimethylenedithiol, dithiotrimethyleneglycol, trimethylenedithioglycol, 1,3-propanedimercaptan, unii-r4luj82u52, fema no. 3588, 1,3-propane dithiol
PubChem CID 8013
ChEBI CHEBI:44864
IUPAC Name propane-1,3-dithiol
SMILES C(CS)CS
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Products 3
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AAA1526106
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Thermo Scientific Chemicals
A1526106
5 g
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AAA1526114
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Thermo Scientific Chemicals
A1526114
25 g
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AAA1526122
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Thermo Scientific Chemicals
A1526122
100 g
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Description

Description

1,3-Propanedithiol is used as a reagent in the preparation of thioketals and thioacetals. It acts as a flavoring agent. It is used as a precursor in the synthesis of cyclic dithioacetal (1,3-dithiane) derivatives of carbonyl compounds. It is involved in the preparation of diiron propanedithiolate hexacarbonyl by reacting reaction with triiron dodecacarbonyl. Further, it is used for the protection of aldehydes and ketones through their reversible formation of dithianes. In addition to this, it reacts with metal ions to form chelate rings.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
1,3-Propanedithiol is used as a reagent in the preparation of thioketals and thioacetals. It acts as a flavoring agent. It is used as a precursor in the synthesis of cyclic dithioacetal (1,3-dithiane) derivatives of carbonyl compounds. It is involved in the preparation of diiron propanedithiolate hexacarbonyl by reacting reaction with triiron dodecacarbonyl. Further, it is used for the protection of aldehydes and ketones through their reversible formation of dithianes. In addition to this, it reacts with metal ions to form chelate rings.

Solubility
Slightly soluble in water. Miscible with alcohol, ether, chloroform, etherMiscible with alcohol, ether, chloroform and ether. Slightly miscible with water.

Notes
Store in a cool place. Incompatible with bases, oxidizing agents, reducing agents and alkali metals.
Specifications

Chemical Identifiers

109-80-8
108.217
ZJLMKPKYJBQJNH-UHFFFAOYSA-N
8013
propane-1,3-dithiol
C3H8S2
MFCD00004904
1,3-propanedithiol, 1,3-dimercaptopropane, trimethylene dimercaptan, trimethylenedithiol, dithiotrimethyleneglycol, trimethylenedithioglycol, 1,3-propanedimercaptan, unii-r4luj82u52, fema no. 3588, 1,3-propane dithiol
CHEBI:44864
C(CS)CS

Specifications

109-80-8
1.077
63°C (145°F)
C3H8S2
MFCD00004904
UN3334
14,7801
Slightly soluble in water; Miscible with alcohol,ether,chloroform,etherMiscible with alcohol,ether,chloroform and ether; Slightly miscible with water.
C(CS)CS
108.217
CHEBI:44864
97%
-79°C
168°C to 170°C
Stench
1.54
5 g
1071197
1,3-propanedithiol, 1,3-dimercaptopropane, trimethylene dimercaptan, trimethylenedithiol, dithiotrimethyleneglycol, trimethylenedithioglycol, 1,3-propanedimercaptan, unii-r4luj82u52, fema no. 3588, 1,3-propane dithiol
ZJLMKPKYJBQJNH-UHFFFAOYSA-N
propane-1,3-dithiol
8013
108.23
1,3-Propanedithiol
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Safety and Handling

Safety and Handling

GHS H Statement
H315-H319-H335-H227
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Combustible liquid.

P210-P233-P235-P240-P241-P242-P243-P261-P264b-P270-P271-P280-P301+P310-P303+P361+P353-P304+P340-P305+P351+P338-P312-P330-P332+P313-P363-P370+P378q-P501c

H226-H301-H315-H319-H335

DOTInformation : Hazard Class: 3; Packaging Group: III

EINECSNumber : 203-706-9

RTECSNumber : TZ2585500

TSCA : Yes

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only