Benzyl mercaptan

It is a common laboratory alkylthiol that occurs in trace amounts naturally.

The initially formed isothiouronium salt must be subjected to alkaline hydrolysis to obtain the thiol.

It has been identified in boxwood (Buxus sempervirens L.) and is known to contribute to the smoky aroma of certain wines.

Debenzylation can be effected by dissolving metal reduction:[4] Condensed tannins undergo acid-catalyzed cleavage in the presence of benzyl mercaptan.

Methoxy-substituted benzyl mercaptans have been developed that cleave easily, are recyclable, and are odorless.

Skeletal formula benzyl mercaptan
Ball-and-stick model of the benzyl mercaptan molecule
NFPA 704 four-colored diamond Health 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroform Flammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuel Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen Special hazards (white): no code