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1-(5-tert-Butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea

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1-(5-tert-Butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea manufacturers

  • Tebuthiuron
  • Tebuthiuron  pictures
  • 2026-07-14
  • CAS:34014-18-1
  • Min. Order: 1kg
  • Purity: 95
  • Supply Ability: 20tons
1-(5-tert-Butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea Basic information
Product Name:1-(5-tert-Butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea
Synonyms:Perflan;Perfmid;Preflan;Prefmid;sha105501;1-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea/TEBUTHIURON;tebuthiuron (ISO) 1-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea;tebuthiuron (bsi,iso,ansi,wssa)
CAS:34014-18-1
MF:C9H16N4OS
MW:228.31
EINECS:251-793-7
Product Categories:Pesticides intermediate;Herbicides;TA - TEPesticides&Metabolites;Urea structure;Alpha sort;Pesticides&Metabolites;Q-ZAlphabetic;Alphabetic
Mol File:34014-18-1.mol
1-(5-tert-Butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea Structure
1-(5-tert-Butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea Chemical Properties
Melting point 161-164°C
density 1.2080 (rough estimate)
refractive index 1.6390 (estimate)
storage temp. 0-6°C
form Solid
pka13.36±0.46(Predicted)
color White to Light yellow
Water Solubility 2.3g/L(temperature not stated)
λmax255nm(lit.)
Merck 14,9095
BRN 527479
Henry's Law Constant6.9×104 mol/(m3Pa) at 25℃, Keshavarz et al. (2022)
Exposure limitsLC50 (96-hour) for bluegill sunsh 112 mg/L, rainbow trout 144 mg/L, goldsh and fathead minnow >160 mg/L (Hartley and Kidd, 1987); acute oral LD50 for rats 644 mg/kg (Ashton and Monaco, 1991).
Major Applicationagriculture
environmental
InChI1S/C9H16N4OS/c1-9(2,3)6-11-12-8(15-6)13(5)7(14)10-4/h1-5H3,(H,10,14)
InChIKeyHBPDKDSFLXWOAE-UHFFFAOYSA-N
SMILESCNC(=O)N(C)c1nnc(s1)C(C)(C)C
CAS DataBase Reference34014-18-1(CAS DataBase Reference)
NIST Chemistry ReferenceTebuthiuron(34014-18-1)
EPA Substance Registry SystemTebuthiuron (34014-18-1)
Safety Information
Hazard Codes Xn;N,N,Xn
Risk Statements 22-50/53
Safety Statements 37-60-61
RIDADR UN 3077
WGK Germany 3
RTECS YS4250000
HazardClass 9
PackingGroup III
HS Code 29349990
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Hazardous Substances Data34014-18-1(Hazardous Substances Data)
ToxicityLD50 in mice, rats, rabbits (mg/kg): 579, 644, 286 orally (Todd)
MSDS Information
1-(5-tert-Butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea Usage And Synthesis
UsesTebuthiuron is an nonselective broad spectrum herbicide used to control weeds, woody and herbaceous plants.
UsesHerbicide.
UsesNonselective herbicide used to control herbaceous and woody plants on noncrop land.
DefinitionChEBI: Tebuthiuron is an organonitrogen heterocyclic compound and an organosulfur heterocyclic compound.
Production MethodsTebuthiuron is produced commercially through a multi-step chemical synthesis that constructs its urea-based herbicidal structure. The process begins with the preparation of key intermediates such as substituted phenyl isocyanates and methylamines, which are reacted under controlled conditions to form the active tebuthiuron molecule.
General DescriptionColorless odorless crystals. Non corrosive. Used as an herbicide.
Reactivity ProfileA urea, thiadiazole derivative.
Agricultural UsesHerbicide: Tebuthiuron is a broad-spectrum herbicide that is used to control weeds in non-cropland areas, range lands, rights-of-way and industrial sites. In grasslands and sugar cane it controls woody and herbaceous plants and weeds such as alfalfa, bluegrasses, chickweed, clover, dock, goldenrod and mullein. Not approved for use in EU countries[ 115]. Registered for use in the U.S.
Trade nameBRULAN®; BRUSH-BULLET®; E-103®; GRASLAN®; HERBEC®; HERBIC®; PERFLAN®; RECLAIM; SHA-105501®; SPIKE®; SPRAKIL®; TEBULAN®; TIUROLAN®
Mechanism of actionSystemic, low selectivity, absorbed by roots and translocated. Inhibits photosynthesis (photosystem II).
Environmental FateSoil. In microbially active soils, tebuthiuron is degraded via demethylation. The average half-life in soil 12–15 months in areas receiving 60 inches of rainfall a year (Humburg et al., 1989).
When tebuthiuron was applied to a rangeland at a rate of 0.84 kg/ha, 38% remained after 21 months (Emmerich et al., 1984).
Groundwater . According to the U.S. EPA (1986) tebuthiuron has a high potential to leach to groundwater .
Plant. Degrades in plants via N-demethylation and hydroxylation of the t-butyl sidechain (Hartley and Kidd, 1987; Humburg et al., 1989).
Pesticide TypeHerbicide
1-(5-tert-Butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea Preparation Products And Raw materials
Raw materials2,2-Dimethylpropionic acid hydrazide-->Pivalic acid-->Methylamine-->1,3-Dimethylurea
Tag:1-(5-tert-Butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea(34014-18-1) Related Product Information
Sulfometuron-methyl tert-Butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea 2-Amino-5-tert-butyl-1,3,4-thiadiazole Benzthiazuron Methylurea 1,3-Dimethylurea TEBUTHIURON SOLUTION 100UG/ML IN ACETONITRILE 1ML TEBUTHIURON SOLUTION 100UG/ML IN T-BUTYLMETHYL ETHER 1ML TEBUTHIURON SOLUTION 100UG/ML IN T-BUTYLMETHYL ETHER 5X1ML TEBUTHIURON SOLUTION 100UG/ML IN T-BUTYLMETHYL ETHER 5ML BUTHIDAZOLE 1-(5-tert-Butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea 2-Amino-1,3,4-thiadiazole 2-Amino-5-methyl-1,3,4-thiadiazole 2-Amino-5-ethyl-1,3,4-thiadiazole 5-isopropyl-1,3,4-thiadiazol-2-amine