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-012447 |
Molecular Formula: C6H3D10NS2 |
Molecular Weight: 173.4 |
Chemical Structure |
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Description | An isotope labelled metabolite of a mixed disulfide S-(N,N-diethyldithiocarbamoyl)-N-acetyl-L-cysteine, an antimutagenic mixed disulfide from disulfiram. |
Synonyms | Methyl diethyldithiocarbamate D10 |
IUPAC Name | methyl N,N-bis(1,1,2,2,2-pentadeuterioethyl)carbamodithioate |
Related CAS | 686-07-7 (unlabelled) |
Canonical SMILES | CCN(CC)C(=S)SC |
InChI | InChI=1S/C6H13NS2/c1-4-7(5-2)6(8)9-3/h4-5H2,1-3H3/i1D3,2D3,4D2,5D2 |
InChI Key | JYRXPFCUABYLPD-IZUSZFKNSA-N |
Purity | 95% by HPLC; 98% atom D |
Methyl diethyldithiocarbamate-[d10], a deuterated derivative of the organosulfur compound, finds diverse applications in scientific realms. Here are the key applications:
Pharmacokinetic Studies: Serving as an internal standard in pharmacokinetic and metabolic investigations, Methyl diethyldithiocarbamate-[d10] plays a crucial role in accurately quantifying its concentration in biological samples through mass spectrometry. This precise quantification facilitates the monitoring of drug absorption, distribution, metabolism, and excretion in both preclinical and clinical studies, shedding light on intricate drug dynamics.
Chemical Research: Within the realm of chemical exploration, Methyl diethyldithiocarbamate-[d10] is a valuable tool for delving into reaction mechanisms and isotope effects. With its deuterated form offering insights into Methyl diethyldithiocarbamate's behavior under diverse chemical conditions, researchers can glean essential information for optimizing chemical synthesis pathways and unraveling reactivity mysteries, paving the way for breakthroughs in synthetic methodologies.
Environmental Monitoring: Deployed in environmental investigations, Methyl diethyldithiocarbamate-[d10] serves as a potent compound for tracking the fate of dithiocarbamates in ecosystems. By utilizing this compound as a tracer, researchers can meticulously monitor its degradation, mobility, and accumulation in soil and water, contributing to a comprehensive assessment of the environmental consequences and potential risks associated with dithiocarbamate usage in agricultural and industrial settings.
Toxicology Studies: In the realm of toxicological scrutiny, Methyl diethyldithiocarbamate-[d10] acts as a reference standard for evaluating the toxicity and safety profiles of related compounds. By comparing its effects with those of the non-deuterated variant, researchers can dissect the role of isotopic substitution in toxicity, furnishing insights crucial for developing safer chemical alternatives and facilitating regulatory assessments to safeguard public health and environmental integrity.
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