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Benzyl methyl disulfide

CAS No.:699-10-5
Product Grade: Industrial Grade
Purity / Assay: ≥98.0%
Molecular Formula:C₈H₁₀S₂
Molecular Weight:170.3 g/mol
Synonym(s):Methyl benzyl disulfide; Disulfide, methyl phenylmethyl; Benzyldithiomethane; [(Methyldisulfanyl)methyl]benzene

Benzyl methyl disulfide, identified by CAS number 699-10-5, is a specialized organosulfur compound characterized by its distinct unsymmetrical disulfide bridge connecting a benzyl group and a methyl group. This clear to pale yellow liquid is recognized for its potent and characteristic sulfurous aroma, which is often associated with natural volatile components found in Allium species like garlic and onions. As a member of the disulfide family, it exhibits unique chemical reactivity, particularly in redox processes and radical-mediated reactions, making it a valuable building block in organic chemistry.

In industrial and research settings, the compound is valued for its specific structural properties and its role as an intermediate in the synthesis of more complex sulfur-containing molecules. Handling this material requires standard laboratory safety protocols, including the use of appropriate personal protective equipment and ventilation, due to its strong odor and potential for irritation. Its stability under controlled conditions allows for precise application in various chemical processes where sulfur functionalization is required.

• In the flavor and fragrance industry, Benzyl methyl disulfide is utilized as a high-potency flavoring agent to impart authentic savory, alliaceous, and roasted notes to food products. Its intense profile is particularly effective in recreating the complex taste and aroma of cooked garlic and onions, where even minute concentrations can significantly enhance the sensory characteristics of seasonings, sauces, and prepared meals.

• Within the field of organic synthesis, this compound serves as a versatile reagent for the introduction of methylthio or benzylthio moieties into various molecular frameworks. Researchers utilize its reactive disulfide bond to facilitate cross-coupling reactions and the preparation of thioethers, which are essential components in the development of specialized polymers, agricultural chemicals, and advanced materials.

• The compound is also employed in analytical chemistry and food science research as a reference standard for the identification and quantification of volatile sulfur compounds in natural extracts. Its presence in the metabolic pathways of certain plants makes it a subject of study for understanding the biosynthetic origins of sulfur-containing secondary metabolites and their impact on the nutritional and medicinal properties of botanical ingredients.

25kg/drum, 180kg/drum, IBC Drum
CAS No.: 699-10-5

Product Name: Benzyl methyl disulfide

Purity / Assay:≥98.0%
Molecular Formula:C₈H₁₀S₂
Molecular Weight:170.3 g/mol
EINECS No.:211-826-8
Synonym(s):Methyl benzyl disulfide; Disulfide, methyl phenylmethyl; Benzyldithiomethane; [(Methyldisulfanyl)methyl]benzene

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