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TIOCARBAZIL

CAS No.
36756-79-3
Chemical Name:
TIOCARBAZIL
Synonyms
m-3432;DREPAMON;Tiocarbenil;TIOCARBAZIL;tiocarbazil (bsi,iso);C17585000 Tiocarbazil;Tiocarbazil in Acetonitrile;S-benzyl di-sec-butylthiocarbamate;Tiocarbazil 10.0 μg/ml Acetonitrile;Prosulfocarb Impurity 8(Tiocarbazil)
CBNumber:
CB3192915
Molecular Formula:
C16H25NOS
Molecular Weight:
279.44
MDL Number:
MFCD00145410
MOL File:
36756-79-3.mol
Last updated:2026-07-31 15:25:14

TIOCARBAZIL Properties

Melting point 25°C
Boiling point 131 °C
Density 1.0443 (rough estimate)
refractive index 1.7000 (estimate)
pka -1.22±0.70(Predicted)
Water Solubility 2.5mg/L(30 ºC)
FDA UNII UO440RHO7T
EPA Substance Registry System Tiocarbazil (36756-79-3)

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Environment (GHS09)
GHS07,GHS09
Signal word  Warning
Hazard statements  H315-H335-H312-H411-H319
Precautionary statements  P264-P280-P302+P352-P321-P332+P313-P362-P280-P302+P352-P312-P322-P363-P501-P264-P280-P305+P351+P338-P337+P313P
HS Code  29302000

TIOCARBAZIL price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
AHH MT-59529 Tiocarbazil 97% 0.5g $480 2026-05-26 Buy
American Custom Chemicals Corporation PST0000376 TIOCARBAZIL 98.00% 36756-79-3 0.5G $1155 2021-12-16 Buy
Product number Packaging Price Buy
MT-59529 0.5g $480 Buy
PST0000376 0.5G $1155 Buy

TIOCARBAZIL Chemical Properties, Uses, Production

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

TIOCARBAZIL Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 24)
Supplier Tel Email Country ProdList Advantage
Shanghai Kewel Chemical Co., Ltd. 021-64609169 18901607656 greensnown@163.com China 9883 50
Alta Scientific Co., Ltd. 022-6537-8550 15522853686 sales@altasci.com.cn China 4508 55
Shandong Xiya Chemical Co., Ltd. 4009903999 13395398332 sales@xiyashiji.com China 20788 60
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 sales@rrkchem.com China 57336 58
Shanghai Jiegu Biotechnology Co., Ltd. 021-51698675 sales@jiejiegroup.com China 8198 58
TCI (Shanghai) Chemical Trading Co., Ltd. 021-61109150 sales@tcisct.com China 29717 58
Shanghai Bikai Technology Co. , Ltd. 18516304666 christina.feng@cpachem-sh.com China 3099 58
Huayin Sample Biological Technology Co. LTD 13892502238 1453186328@qq.com China 929 58
LGC Science (Shanghai) Ltd. 17717235263 17717235263 offer.de@lgcgroup.com China 38135 58
DAYANG CHEM (HANGZHOU) CO.,LTD +86-88938639 +86-17705817739 info@dycnchem.com China 53589 58
TIOCARBAZIL di-sec-butylthio-carbamicacis-benzylester m-3432 n,n-di-sec-butyl-s-benzylthiocarbamate s-benzyln,n-di-sec-butylthiocarbamate DREPAMON tiocarbazil (bsi,iso) N,N-Bis(1-methylpropyl)thiocarbamic acid S-benzyl ester Tiocarbenil S-benzyl di-sec-butylthiocarbamate Carbamothioic acid, N,N-bis(1-methylpropyl)-, S-(phenylmethyl) ester S-Benzyl di-sec-Butylthiocarbamate (Tiocarbazil) Prosulfocarb Impurity 8(Tiocarbazil) Tiocarbazil in Acetonitrile C17585000 Tiocarbazil Tiocarbazil 10.0 μg/ml Acetonitrile Tiocarbazil 100 μg/mL in Acetonitrile 36756-79-3 C16H25NOS