25057-89-0
Chemical Structure
Bentazone
- CAS. Nr.: 25057-89-0
- Formula:C10H12N2O3S
- Molecular Weight:240.28
IUPAC Name: 3-isopropyl-1H-benzo[c][1,2,6]thiadiazin-4(3H)-one 2,2-dioxide
InChIKey: ZOMSMJKLGFBRBS-UHFFFAOYSA-N
SMILES: O=C1N(C(C)C)S(NC2=CC=CC=C12)(=O)=O
Biological Activity: Bentazone is a selective post-emergence herbicide and a Photosystem II inhibitor targeting the quinone B binding site, with activity against broadleaf weeds. Bentazone interferes with photosynthetic electron transport, blocks sunlight-dependent energy production, and acts as a phytotoxin to induce leaf damage, growth inhibition, lipid peroxidation, and reduced chlorophyll content[1][2][3].
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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Bentazone | Bentazone is a selective post-emergence herbicide and a Photosystem II inhibitor targeting the quinone B binding site, with activity against broadleaf weeds. Bentazone interferes with photosynthetic electron transport, blocks sunlight-dependent energy production, and acts as a phytotoxin to induce leaf damage, growth inhibition, lipid peroxidation, and reduced chlorophyll content. | |||||||||||||||||||||
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Bentazone (Standard) | 98.65% | Bentazone (Standard) is the analytical standard of Bentazone (HY-B2039). This product is intended for research and analytical applications. Bentazone is a selective post-emergence herbicide and a Photosystem II inhibitor targeting the quinone B binding site, with activity against broadleaf weeds. Bentazone interferes with photosynthetic electron transport, blocks sunlight-dependent energy production, and acts as a phytotoxin to induce leaf damage, growth inhibition, lipid peroxidation, and reduced chlorophyll content. | ||||||||||||||||||||
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Bentazone-d7 | 98.76% | Bentazone-d7 is the deuterated-labeled Bentazone (HY-B2039). Bentazone is a selective post-emergence herbicide and a Photosystem II inhibitor targeting the quinone B binding site, with activity against broadleaf weeds. Bentazone interferes with photosynthetic electron transport, blocks sunlight-dependent energy production, and acts as a phytotoxin to induce leaf damage, growth inhibition, lipid peroxidation, and reduced chlorophyll content. | ||||||||||||||||||||
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- [1]. Ali L, et al. The prospect of bentazone-tolerant soybean for conventional cultivation. Agronomy. 2020;10(11):1650.
- [2]. Shi L, et al. Herbicide applications increase greenhouse gas emissions of alfalfa pasture in the inland arid region of northwest China. PeerJ. 2020;8:e9231. [Content Brief]
- [3]. Qiao Y, et al. Multiple Metabolism Pathways of Bentazone Potentially Regulated by Metabolic Enzymes in Rice. Journal of agricultural and food chemistry. 2023 Jul 26;71(29):11204-11216.
