AgrochemicalsAldicarb Impurity 2
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Aldicarb sulfoxide
CAT. NO.:SAA-06-B
CAS NO.:1646-87-3
- Description
- Datasheet
- Additional information
Description
Aldicarb Impurity 2
Chemical Name | Aldicarb sulfoxide |
Catalog Number | SAA-06-B |
Parent AI | Aldicarb |
Synonyms | [(E)-(2-methyl-2-methylsulfinylpropylidene)amino] N-methylcarbamate |
CAS Number | 1646-87-3 |
Molecular Formula | C7H14N2O3S |
Molecular Weight | 206.27 |
Appearance | Solid powder |
Melting Point | |
Shipping & Storage Information
|
StorageDry, dark and at 0 – 4 C for short term (days to weeks) or -20 C for long term (months to years).
Shipping: Free Shipping at Room Temperature in INDIA, may vary elsewhere Stability: Datasheet |
Solubility | Soluble in DMSO |
Stability | Stable under recommended storage conditions |
Category | Agrochemical Impurity Standard/Metabolites; |
Description &Applications | Aldicarb sulfoxide is a metabolite and degradation product of the carbamate pesticide aldicarb. Aldicarb sulfoxide (10 μg/ml) reduces the number of male T. semipenetrans second-stage larvae that reach the third, fourth, and adult stages of development. It inhibits carboxylesterase and cholinesterase in zebrafish (IC50 = 10 μM for both). Aldicarb sulfoxide, cholinesterase inhibitor in insects, is formed from Temik during initial oxidation. It is persistent in soil and is rapidly translocated in plants. Aldicarb sulfoxide is a metabolite of aldicarb. |
Aldicarb Sulfoxide: Unveiling the Science Behind an Important Pesticide Metabolite
In the realm of agricultural chemistry, the study of pesticides has significantly contributed to enhancing crop yields and protecting agricultural resources. One such compound that has garnered attention is Aldicarb sulfoxide, a metabolite derived from Aldicarb, a carbamate-class pesticide. Aldicarb sulfoxide plays a pivotal role in understanding the behavior and impact of pesticides in the environment and has sparked interest in both scientific and regulatory circles.
Chemical Structure and Formation: Aldicarb sulfoxide, chemically known as (RS)-2-Methyl-2-(methylthio)propanal O-(methylcarbamoyl)oxime sulfoxide, is the result of the metabolic transformation of Aldicarb. Aldicarb itself is used to control a wide range of insect pests, predominantly in crops such as cotton, citrus fruits, and vegetables. When Aldicarb is applied to the soil, it undergoes biotransformation by plants and soil microorganisms, leading to the formation of its primary metabolite, Aldicarb sulfoxide.
Metabolism and Biological Activity: Aldicarb sulfoxide is formed as a result of the oxidation of Aldicarb, primarily mediated by soil microorganisms. This metabolite exhibits distinct chemical properties from its precursor and has different biological activities. It is considered less toxic to mammals and exhibits a reduced ability to inhibit the enzyme acetylcholinesterase, which is essential for nerve impulse transmission. This metabolic transformation is crucial for understanding the fate of Aldicarb in the environment and its potential impact on non-target organisms.
Environmental Fate and Concerns: The behavior of Aldicarb sulfoxide in the environment is of paramount importance due to its potential persistence and potential risk to ecosystems. Research has shown that Aldicarb sulfoxide can undergo further transformation to Aldicarb sulfone, which is even less toxic than Aldicarb sulfoxide. However, both these metabolites can persist in soil and may leach into groundwater, raising concerns about water contamination and potential human exposure.
Regulation and Safety: The regulatory status of Aldicarb and its metabolites varies among different countries. Regulatory bodies evaluate the safety and environmental impact of pesticides, including their metabolites, before allowing their use in agriculture. The scientific community continues to conduct research to better understand the behavior of Aldicarb sulfoxide and its potential long-term effects on ecosystems and human health. This information is crucial for making informed decisions about the appropriate use and regulation of pesticides.
Advancements and Alternatives: As agricultural practices evolve, researchers are actively exploring alternatives to traditional pesticides, driven by concerns about their environmental impact. Integrated Pest Management (IPM) approaches, which combine various strategies including biological control and crop rotation, aim to reduce reliance on chemical pesticides like Aldicarb. These strategies not only minimize the use of potentially harmful compounds but also contribute to sustainable and resilient agricultural systems.
Additional information
Pack Size | 50mg |
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