- Metamitron
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- $36.00 / 25mg
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2025-09-11
- CAS:41394-05-2
- Min. Order:
- Purity: 99.84%
- Supply Ability: 10g
- Metamitron
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- $0.00 / 25kg
-
2025-06-26
- CAS:41394-05-2
- Min. Order: 1kg
- Purity: 99
- Supply Ability: 20tons
- Metamitron
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- $50.00 / 1kg
-
2025-05-23
- CAS:41394-05-2
- Min. Order: 1kg
- Purity: 99
- Supply Ability: 5000
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| | Metamitron Basic information |
| | Metamitron Chemical Properties |
| 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 | | Toxicity | LD50 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 |
| Uses | Herbicide. | | Definition | ChEBI: 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. | | General Description | 4-Amino-3-methyl-6-phenyl-1,2,4-triazin-5-one, commonly known as metamitron, is a pesticide having low polarity and is hydrophobic in nature. Its pKa value is 2.9. | | Agricultural Uses | Herbicide: 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 name | BAY 6676®; BAY-DRW 1139®; DRW
1139®; GALAHAD®; GOLDBEET®; GOLTIX®;
GOLTIX® 90; GOLTIX® SUPER; GOLTIX® WG;
MM 70®; HERBRAK®; MARQUISE®; SKATER®;
TORERO® (metamitron + ethofumesate) | | Metabolic pathway | Degradation 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). |
| | Metamitron Preparation Products And Raw materials |
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