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Thiazafluron

CAS No.
25366-23-8
Chemical Name:
Thiazafluron
Synonyms
dmttu;gs29296;erbotan;thiazfluron;Thiazafluron;Thiazafluoron;thiazafluron (bsi,iso);C17460000 Thiazafluron;Thiazafluron in Acetone;THIAZAFLURON PESTANAL, 250 MG
CBNumber:
CB1448258
Molecular Formula:
C6H7F3N4OS
Molecular Weight:
240.21
MDL Number:
MFCD00078722
MOL File:
25366-23-8.mol
Last updated:2026-09-12 18:49:14

Thiazafluron Properties

Melting point 136.5°C
Density 1.507±0.06 g/cm3(Predicted)
pka 13.14±0.46(Predicted)
Water Solubility 2.096g/L(20 ºC)
BRN 806900
Henry's Law Constant 3.2×104 mol/(m3Pa) at 25℃, MacBean (2012)
EWG's Food Scores 1
FDA UNII WX8ID0K28Q

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Environment (GHS09)
GHS07,GHS09
Signal word  Warning
Hazard statements  H302-H410
Precautionary statements  P273-P501
Hazard Codes  Xn,N
Risk Statements  22-50/53
Safety Statements  60-61
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS  XI3760000
HS Code  29349990
Toxicity mouse,LD50,oral,630mg/kg (630mg/kg),"Agrochemicals Handbook," with updates, Hartley, D., and H. Kidd, eds., Nottingham, Royal Soc of Chemistry, 1983-86Vol. A392, Pg. 1983,

Thiazafluron price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
aablocks AA00BD93 THIAZAFLURON 25366-23-8 250mg $278 2021-12-16 Buy
Product number Packaging Price Buy
AA00BD93 250mg $278 Buy

Thiazafluron Chemical Properties, Uses, Production

Definition

ChEBI: Thiazafluron is an organonitrogen heterocyclic compound and an organosulfur heterocyclic compound.

Production Methods

Thiazafluron is produced commercially through a multi-step synthesis that constructs its substituted urea-thiadiazole structure. The process begins with the formation of a 1,3,4-thiadiazole ring, typically synthesised from thiosemicarbazide derivatives. This ring is then functionalised with a trifluoromethyl group to enhance herbicidal potency and environmental stability. The key intermediate is subsequently reacted with dimethylurea or its derivatives to form the final active compound, thiazafluron.

Mechanism of action

Non-selective, Photosynthetic electron transport inhibitor.

Pesticide Type

Herbicide

Thiazafluron Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 28)
Supplier Tel Email Country ProdList Advantage
Suzhou Highfine Biotech Co., Ltd 0512-69209928 18796809688 zhouyingxiang@highfine.com China 473 75
Shanghai Kewel Chemical Co., Ltd. 021-64609169 18901607656 greensnown@163.com China 9883 50
Hubei Yangxin Medical Technology Co., Ltd. 15374522761 3003392093@yongstandards.com China 9995 55
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 8195 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
DAYANG CHEM (HANGZHOU) CO.,LTD +86-88938639 +86-17705817739 info@dycnchem.com China 53736 58
2-(n,n’-dimethylureido)-5-trifluoromethyl-1,3,4-thiadiazole 4-thiadiazole,2-(n,n’-dimethylureido)-5-trifluoromethyl-3 erbotan gs29296 n,n’-dimethyl-n-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)urea 1,3-DIMETHYL-1-(5-TRIFLUOROMETHYL-1,3,4-THIADIAZOL-2-YL)-UREA thiazafluron (bsi,iso) thiazfluron (ISO) 1,3-dimethyl-1-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)urea thiazfluron THIAZAFLURON PESTANAL, 250 MG 1,3-dimethyl-1-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)urea,thiazfluron (ISO) Urea, N,N'-dimethyl-N'-[5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl]- Thiazafluron in Acetone C17460000 Thiazafluron Thiazafluron 100 μg/ml Acetonitrile Thiazafluoron dmttu Thiazafluron 25366-23-8 C6H7F3N4OS Alpha sort Herbicides Pesticides&Metabolites Q-ZAlphabetic TF - TOPesticides&Metabolites Urea structure