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Metamitron

Release time:2021-12-10
Abstract:Metamitron

Metamitron 98TC -2.png

Metamitron 98TC


Metamitron Basic information
Product Name:Metamitron
Synonyms:3-methyl-4-amino-6-phenyl-1,2,4-triazin(4h)-on;3-Methyl-4-amino-6-phenyl-1,2,4-triazin(4H)-one;4-Amino-3-methyl-6-phenyl-1,2,4-triazin-5(4H)-one;4-amino-3-methyl-6-phenyl-as-triazin-5(4h)-on;as-Triazin-5(4H)-one, 4-amino-3-methyl-6-phenyl-;Bay-drw 1139;bay-drw1139;Countdown
CAS:41394-05-2
MF:C10H10N4O
MW:202.21
EINECS:255-349-3
Product Categories:pharmaceutical intermediate Metamitron;farm chemicals;HERBICIDE;Building  Blocks;Heterocyclic  Building  Blocks;Triazines;Heterocyclic Compounds
Mol File:41394-05-2.mol
Metamitron Structure

               


Metamitron Chemical Properties
Melting point 165-170 °C
Boiling point 340.33°C (rough estimate)
density 1.2165 (rough estimate)
refractive index 1.6300 (estimate)
Fp 11 °C
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
pka1.54±0.20(Predicted)
form neat
Water Solubility 1.8g/L(20 ºC)
λmax312nm(CH3CN)(lit.)
Merck 14,5924
BRN 613129
CAS DataBase Reference41394-05-2(CAS DataBase Reference)
NIST Chemistry Reference1,2,4-Triazin-5(4h)-one, 4-amino-3-methyl-6-phenyl-(41394-05-2)
EPA Substance Registry SystemMetamitron (41394-05-2)

               


Safety Information
Hazard Codes Xn,N,T,F
Risk Statements 22-50-39/23/24/25-23/24/25-11
Safety Statements 61-45-36/37
RIDADR UN 3077 9/PG 3
WGK Germany 2
RTECS XZ3015000
HazardClass 9
PackingGroup III
HS Code 29336990
ToxicityLD50 orally in male, female rats, male, female mice:  3343, 1832, 1450, 1463 mg/kg; dermally in rats:  >500 mg/kg; LC50 (4 hr) in rats, mice, hamsters (mg/m3):  >331, >206, >206 by inhalation (Lembrich)
     

Metamitron Usage And Synthesis
UsesHerbicide.
DefinitionChEBI: A member of the class of 1,2,4-triazines that is 1,2,4-triazin-5(4H)-one substituted by an amino group at position 4, a methyl group at position 3 and a phenyl group at position 6.
Agricultural UsesHerbicide: Metamitron is a selective systemic herbicide that is absorbed through roots and leaves and inhibits photosynthesis. It is used to control grasses and broadleaf weeds in sugar beets and fodder beets. Not currently registered in the U.S. Used in most European countries and having 34 global suppliers .
Trade nameBAY 6676®; BAY-DRW 1139®; DRW 1139®; GALAHAD®; GOLDBEET®; GOLTIX®; GOLTIX® 90; GOLTIX® SUPER; GOLTIX® WG; MM 70®; HERBRAK®; MARQUISE®; SKATER®; TORERO® (metamitron +  ethofumesate)
Metabolic pathwayDegradation of metamitron by photolysis is strongly dependent on solvents and oxygen, and no photoreaction is found in methanol, acetonitrile, and hexane, nor in oxygen-free water. In water solution, photolytic degradation occurs and results in the formation of desaminometamitron and a ring-opening polar benzoylacetyl hydrazine (tentatively assigned).




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