Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
In addition to treating various diseases, isotopes are used for imaging, diagnosis, and newborn screening.
Small molecule compounds labeled with stable isotopes can be used as chemical reference for chemical identification, qualitative, quantitative, detection, etc. Various types of NMR solvents can be used to study the structure, reaction mechanism and reaction kinetics of compounds.
Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
General Information |
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Catalog: BLP-007366 |
Molecular Formula: C8H9D10O2PS3 |
Molecular Weight: 284.5 |
Chemical Structure |
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Description | Disulfoton-[d10] is the labelled analogue of Disulfoton. Disulfoton is an organophosphate acetylcholinesterase inhibitor used as an insecticide. |
Synonyms | Disulfoton D10 (di(ethyl D5)) |
IUPAC Name | 2-ethylsulfanylethylsulfanyl-bis(1,1,2,2,2-pentadeuterioethoxy)-sulfanylidene-λ5-phosphane |
Related CAS | 298-04-4 (unlabelled) |
Canonical SMILES | CCOP(=S)(OCC)SCCSCC |
InChI | InChI=1S/C8H19O2PS3/c1-4-9-11(12,10-5-2)14-8-7-13-6-3/h4-8H2,1-3H3/i1D3,2D3,4D2,5D2 |
InChI Key | DOFZAZXDOSGAJZ-IZUSZFKNSA-N |
Purity | 98% by CP; 98% atom D |
Storage | Store at -20°C |
Disulfoton-[d10], an organophosphate pesticide of paramount significance in research, unveils its diverse applications with a heightened sense of perplexity and burstiness:
Environmental Monitoring: Immersed in the realm of environmental studies, Disulfoton-[d10] emerges as an indispensable ally for monitoring pesticide residues in a plethora of samples. This tagging compound facilitates meticulous tracking and quantification of disulfoton across soil, water, and air, significantly bolstering the evaluation of environmental contamination and the efficacy of remedial actions.
Toxicological Studies: The landscape of toxicology witnesses a profound impact as researchers harness Disulfoton-[d10] to unravel the labyrinthine pathways of disulfoton metabolism and biotransformation within living organisms. This labeled analog acts as a guiding light, shedding illumination on metabolic processes and unveiling metabolites within biological systems. Such knowledge is pivotal for deciphering toxicokinetics and comprehending the potential health ramifications of exposure to disulfoton.
Analytical Method Development: The integration of Disulfoton-[d10] as an internal standard in analytical chemistry catapults the refinement and validation of methods for detecting residual disulfoton to new heights. Its isotopic labeling serves as a calibration mechanism for addressing instrumental fluctuations and enhancing the precision of quantitative analyses, particularly beneficial for laboratories engaged in routine pesticide residue assessments.
Pharmacokinetics in Model Systems: Within the confines of controlled laboratory environments, Disulfoton-[d10] stands as a cornerstone for exploring the absorption, distribution, metabolism, and excretion (ADME) of pesticides in model organisms. A comprehensive grasp of disulfoton pharmacokinetics facilitates the evaluation of safety profiles and regulatory adherence, proving instrumental in risk assessment and the evolution of safer agricultural practices.
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