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Diallyl disulfide-[d10]

General Information
Catalog: BLP-005090
Molecular Formula: C6D10S2
Molecular Weight: 156.34
Chemical Structure
Diallyl disulfide-[d10]
Description Diallyl disulfide-[d10] is deuterium labelled Diallyl disulfide, which is an organosulfur compound derived from garlic and a few other genus Allium plants.
Synonyms Diallyl Disulphide-d10; Allyl Disulfide-d10; Di-2-propenyl Disulfide-d10; 4,5-Dithia-1,7-octadiene-d10; Bis(2-propenyl) disulfide-d10; Di(2-propenyl) Disulfide-d10; Dipropenyl Disulfide-d10; Garlicin-d10; NSC 29228-d10
Related CAS 2179-57-9 (unlabelled)
Storage Store at 2-8°C

Diallyl disulfide-[d10] is a deuterated analog of diallyl disulfide, a compound found in garlic, used across various research and industrial applications. Here are some key applications of Diallyl disulfide-[d10]:

Stable Isotope Labeling: Diallyl disulfide-[d10] is used in mass spectrometry as a stable isotope-labeled compound to study garlic metabolism and biotransformation processes. By incorporating deuterium, it allows for precise tracking and quantification in metabolic studies. This application is crucial for understanding the bioactive properties of garlic and potential health benefits.

Pharmacokinetic Studies: In drug discovery, Diallyl disulfide-[d10] serves as an internal standard or tracer in pharmacokinetic experiments. Its use helps in assessing the absorption, distribution, metabolism, and excretion of novel therapeutic compounds. This data is essential for optimizing dosage forms and ensuring drug safety and efficacy.

Nutritional Research: Researchers use Diallyl disulfide-[d10] to investigate the biological effects of garlic constituents in nutrition studies. By differentiating between dietary metabolites and those formed endogenously, scientists gain insights into the health-promoting properties of garlic. This is particularly important for understanding its role in cardiovascular health and cancer prevention.

Chemical Reaction Mechanisms: Diallyl disulfide-[d10] is employed in studying the reaction mechanisms and kinetics of sulfur-containing compounds. By using the deuterated form, scientists can monitor mechanistic pathways with greater precision. These insights can lead to the development of novel synthetic processes and improved industrial applications involving organosulfur compounds.

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