Date published: 2025-12-31

1-800-457-3801

SCBT Portrait Logo
Seach Input

Allyl methyl sulfide (CAS 10152-76-8)

0.0(0)
Write a reviewAsk a question

CAS Number:
10152-76-8
Molecular Weight:
88.17
Molecular Formula:
C4H8S
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Allyl methyl sulfide functions as a substrate in biochemical research. It acts as a precursor in the synthesis of organosulfur compounds, contributing to the investigation of sulfur-containing molecules and their reactivity. The mechanism of action involves its participation in thiol-disulfide exchange reactions, leading to the formation of various sulfur-containing products. Allyl methyl sulfide plays a role in the modification of proteins and peptides through the introduction of sulfur groups, allowing for the study of their structural and functional changes. Allyl methyl sulfide serves as a model compound for investigating the reactivity of allyl sulfides in organic synthesis, contributing to the understanding of their chemical properties and potential applications in various reactions. Its involvement in the formation of sulfur-containing compounds and its reactivity with biomolecules make it useful for exploring the role of sulfur in biochemical processes and organic chemistry.


Allyl methyl sulfide (CAS 10152-76-8) References

  1. Mechanisms of the preventive properties of some garlic components in the carbon tetrachloride-promoted oxidative stress. Diallyl sulfide; diallyl disulfide; allyl mercaptan and allyl methyl sulfide.  |  Fanelli, SL., et al. 1998. Res Commun Mol Pathol Pharmacol. 102: 163-74. PMID: 10100508
  2. Asymmetric copper-catalyzed.  |  McMillen, DW., et al. 2000. J Org Chem. 65: 2532-6. PMID: 10789467
  3. Allicin and allicin-derived garlic compounds increase breath acetone through allyl methyl sulfide: use in measuring allicin bioavailability.  |  Lawson, LD. and Wang, ZJ. 2005. J Agric Food Chem. 53: 1974-83. PMID: 15769123
  4. Allicin Bioavailability and Bioequivalence from Garlic Supplements and Garlic Foods.  |  Lawson, LD. and Hunsaker, SM. 2018. Nutrients. 10: PMID: 29937536
  5. Allyl methyl sulfide, an organosulfur compound alleviates hyperglycemia mediated hepatic oxidative stress and inflammation in streptozotocin - induced experimental rats.  |  Sujithra, K., et al. 2018. Biomed Pharmacother. 107: 292-302. PMID: 30098547
  6. Identification and Quantification of Volatile Ramson-Derived Metabolites in Humans.  |  Scheffler, L., et al. 2018. Front Chem. 6: 410. PMID: 30255016
  7. Allyl methyl sulfide, a garlic active component mitigates hyperglycemia by restoration of circulatory antioxidant status and attenuating glycoprotein components in streptozotocin-induced experimental rats.  |  Sujithra, K., et al. 2019. Toxicol Mech Methods. 29: 165-176. PMID: 30318971
  8. Biomarkers of food intake for Allium vegetables.  |  Praticò, G., et al. 2018. Genes Nutr. 13: 34. PMID: 30607216
  9. Quantification of Volatile Metabolites Derived From Garlic (Allium sativum) in Human Urine.  |  Scheffler, L., et al. 2019. Front Nutr. 6: 43. PMID: 31111029
  10. Measurement of diallyl disulfide and allyl methyl sulfide emanating from human skin surface and influence of ingestion of grilled garlic.  |  Sato, S., et al. 2020. Sci Rep. 10: 465. PMID: 31949194
  11. Reactivity of allyl methyl sulphide, the in-vitro metabolite of garlic, with some amino acids and with phospholipid involved in viral infections.  |  Sinha, AK., et al. 2022. J Biomol Struct Dyn. 40: 565-571. PMID: 32835626
  12. Quantification of Allyl Methyl Sulfide, Allyl Methyl Sulfoxide, and Allyl Methyl Sulfone in Human Milk and Urine After Ingestion of Cooked and Roasted Garlic.  |  Qin, W., et al. 2020. Front Nutr. 7: 565496. PMID: 33072797
  13. Identification of volatile sulfur odorants emitted from ageing wastewater biosolids.  |  Barczak, RJ., et al. 2022. Chemosphere. 287: 132210. PMID: 34826912
  14. Understanding the Activation of Platelets in Diabetes and Its Modulation by Allyl Methyl Sulfide, an Active Metabolite of Garlic.  |  Malladi, N., et al. 2021. J Diabetes Res. 2021: 6404438. PMID: 35127948

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Allyl methyl sulfide, 5 g

sc-227227
5 g
$20.00