| Identification | Back Directory | [Name]
TIOCARBAZIL | [CAS]
36756-79-3 | [Synonyms]
m-3432
DREPAMON
Tiocarbenil
TIOCARBAZIL
tiocarbazil (bsi,iso)
S-benzyl di-sec-butylthiocarbamate
s-benzyln,n-di-sec-butylthiocarbamate
n,n-di-sec-butyl-s-benzylthiocarbamate
di-sec-butylthio-carbamicacis-benzylester
S-Benzyl di-sec-Butylthiocarbamate (Tiocarbazil)
N,N-Bis(1-methylpropyl)thiocarbamic acid S-benzyl ester
Carbamothioic acid, N,N-bis(1-methylpropyl)-, S-(phenylmethyl) ester | [EINECS(EC#)]
253-190-4 | [Molecular Formula]
C16H25NOS | [MDL Number]
MFCD00145410 | [MOL File]
36756-79-3.mol | [Molecular Weight]
279.44 |
| Hazard Information | Back Directory | [Uses]
Agricultural chemical. | [Definition]
ChEBI: Tiocarbazil is a member of benzenes. | [Production Methods]
Tiocarbazil is commercially produced for agricultural use through the synthesis of thiocarbamate esters, typically involving the reaction of secondary amines with carbon disulphide and benzyl halides under controlled conditions. Its production begins with the formation of a thiocarbamate intermediate by reacting di-sec-butylamine with carbon disulphide, followed by esterification using benzyl chloride or similar benzylating agents to yield tiocarbazil. | [Hazard]
Moderately toxic by skin contact. Low toxicity
by ingestion. | [Mechanism of action]
Selective. Its primary pesticide mode of action is the inhibition of lipid synthesis, which disrupts the formation of plant cell membranes and cuticular waxes. | [Pesticide Type]
Herbicide |
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