AgrochemicalsCarbofuran Impurity 10
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Name:3-Ketocarbofuran CAT. NO.:SAC-05-J CAS NO.:16709-30-1
- Description
- Datasheet
- Additional information
Description
Carbofuran Impurity 10
Chemical Name | 3-Ketocarbofuran |
Catalog Number | SAC-05-J |
Parent AI | Carbofuran |
Synonyms | 3-Oxocarbofuran; 2,2-Dimethyl-7-[[(methylamino)carbonyl]oxy]-3(2H)-benzofuranone; 7-Hydroxy-2,2-dimethyl-3(2H)-benzofuranone Methylcarbamate; (2,2-dimethyl-3-oxo-1-benzofuran-7-yl) N-methylcarbamate |
CAS Number | 16709-30-1 |
Molecular Formula | C₁₂H₁₃NO₄ |
Molecular Weight | 235.24 |
Appearance | Off-White to Pale Yellow Solid |
Melting Point | 175 – 177°C |
Shipping & Storage Information
|
Storage 4°C
Shipping: Free Shipping at Room Temperature in INDIA, may vary elsewhere Stability: Datasheet |
Solubility | Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) |
Stability | Stable under recommended storage conditions |
Category | Standards; Enzyme Activators and Inhibitors; |
Description &Applications | 3-Ketocarbofuran is an organic compound that belongs to the class of carboxylic acids. It is a heterocyclic compound with a five-membered ring structure containing a single oxygen atom. 3-Ketocarbofuran is an important intermediate in the synthesis of several natural products, such as antibiotics and hormones. It has also been used as a reagent in the synthesis of pharmaceuticals, agrochemicals, and food additives. In addition, 3-ketocarbofuran is used in the synthesis of organometallic compounds, polymers, and catalysts. |
References | Abass, K., et al.: Chem-Biol. Interact., 18, 210 (2009); Ambrus, A., et al.: J. Environ. Sci. Heal. B., B40, 297 (2005); Usmani, K., et al.: Chem-Biol. Interact., 150, 221 (2004) |
Among the numerous compounds researched and developed for this purpose, 3-Ketocarbofuran stands out as a powerful tool in the hands of farmers and agronomists. This chemical compound, derived from the furan family, has demonstrated its prowess in protecting crops while raising important questions about its ecological impact.
Chemical Structure and Mechanism of Action: 3-Ketocarbofuran, chemically known as 2,3-dihydro-2,2-dimethyl-7-benzofuranyl methylcarbamate, belongs to the carbamate class of pesticides. Its chemical structure combines a furan ring with a carbamate functional group, conferring potent insecticidal properties. The compound exerts its effects by inhibiting the enzyme acetylcholinesterase in pests, leading to a disruption of the neurotransmitter acetylcholine. This disruption ultimately results in paralysis and death of the targeted insects.
Agricultural Applications: The primary application of 3-Ketocarbofuran is in the protection of a variety of crops against a spectrum of insect pests. Its systemic action allows it to be absorbed by plants, making them toxic to insects that feed on them. This attribute has made 3-Ketocarbofuran particularly effective against soil-dwelling pests such as nematodes and certain beetle larvae. Crops like corn, potatoes, sugarcane, and tobacco have greatly benefited from its use, experiencing increased yields due to reduced pest damage.
Advantages:
- Broad-Spectrum Activity: 3-Ketocarbofuran displays a wide range of efficacy against diverse insect pests, providing a comprehensive solution for pest management.
- Systemic Protection: Its systemic nature ensures that even parts of the plant not directly sprayed with the pesticide receive protection.
- Reduced Pest Resistance: The compound’s mode of action differs from many other pesticides, which helps delay the development of resistance in pest populations.
- Crop Yield Improvement: By preventing pest damage, 3-Ketocarbofuran contributes to higher crop yields, ultimately boosting agricultural productivity.
Environmental Concerns: While 3-Ketocarbofuran offers remarkable benefits to farmers, its usage raises valid ecological concerns. The compound’s persistence in the environment can lead to contamination of soil, water bodies, and non-target organisms. Runoff from agricultural fields treated with 3-Ketocarbofuran can potentially affect aquatic ecosystems, posing risks to aquatic life forms.
Regulation and Safe Usage: Recognizing the potential risks associated with 3-Ketocarbofuran, regulatory bodies in various countries have imposed guidelines for its safe usage. Applicators are required to undergo training, adhere to recommended application rates, and follow pre-harvest intervals to ensure that residues on harvested crops are within permissible limits. Integrated Pest Management (IPM) strategies also promote the judicious use of pesticides, including 3-Ketocarbofuran, in conjunction with other pest control methods.
Additional information
Pack Size | 50mg |
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