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Thidiazuron Suppliers list
Company Name: Capot Chemical Co.,Ltd.
Tel: +86 (0)571-855 867 18
Products Intro: Product Name:5-Phenylcarbamoylamino-1,2,3-thiadiazole
Purity:98% Min. Package:100g;1kg;5kg,10kg,25kg,50kg
Company Name: Mainchem Co., Ltd.
Tel: +86-0592-6210733
Products Intro: Product Name:5-Phenylcarbamoylamino-1,2,3-thiadiazole
Company Name: Hangzhou FandaChem Co.,Ltd.
Tel: 0086 158 5814 5714 (Mobile; WhatsApp; Telegram)
Products Intro: Product Name:Thidiazuron 95%
Purity:95% Package:25kg/drum
Company Name: career henan chemical co
Tel: +86-371-86658258
Products Intro: Product Name:5-Phenylcarbamoylamino-1,2,3-thiadiazole
Purity:99% Package:1kg;2USD
Company Name: Hubei Jusheng Technology Co.,Ltd.
Tel: 86-18871470254
Products Intro: Product Name:thidiazuron
Purity:99% Package:5KG;1KG Remarks:C9H8N4OS

Lastest Price from Thidiazuron manufacturers

Thidiazuron Basic information
Product Name:Thidiazuron
Synonyms:Thidiazuron 250mg [51707-55-2];Avguron;CCG-24904;Dropp SC;Lift;TAG (plant growth regulator);Thidazuron(TDZ);Thidiazuron 0
Product Categories:Aromatics;Heterocycles;Sulfur & Selenium Compounds;NULL;plantgrowth;Cytokinins;Plant Growth Regulators;Plant Tissue Culture;Herbicides;Pesticides;Pesticides&Metabolites;Plant growth regulatorsAlphabetic;TF - TOPesticides&Metabolites;Urea structure;-;Alpha sort;Plant growth regulatorsPesticides&Metabolites;Q-ZAlphabetic
Mol File:51707-55-2.mol
Thidiazuron Structure
Thidiazuron Chemical Properties
Melting point 213°C
density 1.3493 (rough estimate)
refractive index 1.6390 (estimate)
storage temp. 0-6°C
solubility Soluble in DMSO
form neat
Merck 13,9384
BRN 1078092
CAS DataBase Reference51707-55-2(CAS DataBase Reference)
EPA Substance Registry SystemUrea, N-phenyl-N'-1,2,3-thiadiazol- 5-yl-(51707-55-2)
Safety Information
Hazard Codes Xi,N
Risk Statements 36/37/38-51/53
Safety Statements 22-26-36-61
WGK Germany 3
RTECS YU1395000
ToxicityLC50 (96-hour) for bluegill sun?sh, channel cat?sh and rainbow trout >1,000 mg/L (Hartley and Kidd, 1987); acute oral LD50 for rats >5,000 mg/kg (Hartley and Kidd, 1987), 5,350 mg/kg (RTECS, 1985).
MSDS Information
5-Phenylcarbamoylamino-1,2,3-thiadiazole English
SigmaAldrich English
Thidiazuron Usage And Synthesis
UsesThidiazuron is a non-purine containing urea derivative with cytokinin activity. Thidiazuron is used as a cotton defoliant and a plant growth regulator in tissue culture.
UsesCotton defoliant; plant growth regulator in tissue culture.
UsesPlant growth regulator used to defoliate cotton to facilitate harvesting.
Agricultural UsesThidiazuron is substituted urea that is used to defoliate cotton plants. Thidiazuron, which has cytokinin activity, is one of the many harvesting aids needed in agriculture.
Agricultural UsesHerbicide, Defoliant, Plant growth regulator: Used primarily as a cotton defoliant in order to increase the harvest yield. Not applied to food crops. Not approved for use in EU countries. Registered for use in the U.S. U.S. Maximum Allowable Residue Levels for Thidiazuron and its aniline-containing metabolites in or on the following food commodities: [40 CFR 180.403(a)]: cattle, fat 0.4 ppm; cattle, meat 0.4 ppm; cattle, meat byproducts 0.4 ppm; cotton, gin byproducts 24.0 ppm; cotton, undelinted seed 0.3 ppm; goat, fat 0.4 ppm; goat meat 0.4 ppm; goat, meat byproducts 0.4 ppm; hog, fat 0.4 ppm; hog, meat 0.4 ppm; hog, meat byproducts 0.4 ppm; horse, fat 0.4 ppm; horse, meat 0.4 ppm; horse, meat byproducts 0.4 ppm; milk 0.05 ppm; sheep, fat 0.4 ppm; sheep, meat 0.4 ppm; sheep, meat byproducts 0.4 ppm.
Trade nameDAZE®; DEFOLIT®; DROPP®; GINSTAR EC® (thidiazuron + diuron); LEAFLESS® Tthidiazuron; SN 49537®
Safety ProfileModerately toxic by ingestion. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of SOx and NOx.
Environmental FateSoil. The reported half-life in soil is approximately 26–144 days (Hartley and Kidd, 1987).
Photolytic. Rapidly converted to the photoisomer, 1-phenyl-3-(1,2,5-thiadiazol-3- yl)urea (Worthing and Hance, 1991). When thidiazuron adsorbed by soil was exposed to UV light (λ <290 nm), 1-phenyl-3-(1,2,5-thiadiazol-3-yl)urea formed as the majo
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