amicarbazone

Modify Date: 2024-01-02 14:10:07

amicarbazone Structure
amicarbazone structure
Common Name amicarbazone
CAS Number 129909-90-6 Molecular Weight 241.290
Density 1.3±0.1 g/cm3 Boiling Point N/A
Molecular Formula C10H19N5O2 Melting Point 137.5ºC
MSDS N/A Flash Point N/A

 Use of amicarbazone


Amicarbazone(BAY-MKH3586; BAY314666) is a potent inhibitor of photosynthetic electron transport via binding to the Qb domain of photosystem II (PSII); herbicide with a broad spectrum of weed control.IC50 value:Target: PSII inhibitorThe phenotypic responses of sensitive plants exposed to amicarbazone include chlorosis, stunted growth, tissue necrosis, and death. Its efficacy as both a foliar- and root-applied herbicide suggests that absorption and translocation of this compound is very rapid. As a result, its efficacy is susceptible to the most common form of resistance to PSII inhibitors. Nonetheless, amicarbazone has a good selectivity profile and is a more potent herbicide than atrazine, which enables its use at lower rates than those of traditional photosynthetic inhibitors.

 Names

Name amicarbazone
Synonym More Synonyms

 amicarbazone Biological Activity

Description Amicarbazone(BAY-MKH3586; BAY314666) is a potent inhibitor of photosynthetic electron transport via binding to the Qb domain of photosystem II (PSII); herbicide with a broad spectrum of weed control.IC50 value:Target: PSII inhibitorThe phenotypic responses of sensitive plants exposed to amicarbazone include chlorosis, stunted growth, tissue necrosis, and death. Its efficacy as both a foliar- and root-applied herbicide suggests that absorption and translocation of this compound is very rapid. As a result, its efficacy is susceptible to the most common form of resistance to PSII inhibitors. Nonetheless, amicarbazone has a good selectivity profile and is a more potent herbicide than atrazine, which enables its use at lower rates than those of traditional photosynthetic inhibitors.
Related Catalog
References

[1]. Franck E. Dayan, et al. Amicarbazone, a New Photosystem II Inhibitor . ed Science 57(6):579-583. 2009

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Melting Point 137.5ºC
Molecular Formula C10H19N5O2
Molecular Weight 241.290
Exact Mass 241.153870
PSA 94.94000
LogP -0.99
Index of Refraction 1.587
Storage condition 2-8℃

 Safety Information

Hazard Codes Xn
Risk Phrases 20/22
HS Code 2933990090

 Synthetic Route

~97%

amicarbazone Structure

amicarbazone

CAS#:129909-90-6

Literature: Bayer Aktiengesellschaft Patent: US5708184 A1, 1998 ;

 Customs

HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Synonyms

4-amino-N-tert-butyl-5-oxo-3-(propan-2-yl)-4,5-dihydro-1H-1,2,4-triazole-1-carboxamide
4-amino-N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-isobutylbenzenesulfonamide
4-amino-5-i-propyl-2-t-butyl-aminocarbonyl-2,4-dihydro-3H-1,2,4-triazol-3-one
T5NNVNJ BVMX1&1&1 DZ EY1&1
2R-hydroxy-3-[[(4-aminophenyl)sulfonyl](2-methylpropyl)amino]-1S-(phenylmethyl)propylamine
4-Amino-N-(1,1-dimethylethyl)-4,5-dihydro-3-(1-methylethyl)-5-oxo-1H-1,2,4-triazole-1-carboxamide
4-amino-5-isopropyl-2-(tert-butyl-aminocarbonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one
4-Amino-N-tert-butyl-4,5-dihydro-3-isopropyl-5-oxo-1,2,4-1H-triazole-1-carboxamide
4-amino-N-(3-amino-2-hydroxy-4-phenylbutyl)-N-isobutylbenzenesulfonamide
4-amino-N-(1,1-dimethyl-ethyl)-4,5-dihydro-3-(1-methyl-ethyl)-5-oxo-1H-1,2,4-triazole-1-carboxamide
4-amino-N-tert-butyl-5-oxo-3-propan-2-yl-1,2,4-triazole-1-carboxamide
amicarbazone
4-amino-5-(1-methyl-ethyl)-2-(1,1-dimethyl-ethyl-aminocarbonyl)-2,4-dihydro-3H-1,2,4,-triazol-3-one
1H-1,2,4-Triazole-1-carboxamide, 4-amino-N-(1,1-dimethylethyl)-4,5-dihydro-3-(1-methylethyl)-5-oxo-
4-Amino-3-isopropyl-N-(2-methyl-2-propanyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazole-1-carboxamide
4-amino-N-tert-butyl-4,5-dihydro-3-isopropyl-5-oxo-1H-1,2,4-triazole-1-carboxamide
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