General Description
Clear orange oil with a disagreeable odor.
Reactivity Profile
Organosulfides, such as 1,3-DIMERCAPTOPROPANE(109-80-8), are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. This compound may react with oxidizers, bases, reducing agents and alkali metals.
Air & Water Reactions
Highly flammable. Insoluble in water.
Fire Hazard
This chemical is combustible.
Chemical Properties
1,3-Propanedithiol has a sulfur, meaty odor. FEMA indicates that total dithiol added to any food should not exceed 1.0 ppm.
Chemical Properties
colourless to slightly yellow liquid
Occurrence
Reported found in cooked or boiled beef.
Uses
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.
Definition
ChEBI: A dithiol that is propane substituted by thiol groups at positions 1 ans 3.
