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Methyl allyl trisulfide

Basic information Safety Supplier Related

Methyl allyl trisulfide Basic information

Product Name:
Methyl allyl trisulfide
Synonyms:
  • ALLYL METHYL TRISULFIDE
  • ALLYL METHYL TRISULPHIDE
  • METHYL ALLYL TRISULFIDE
  • METHYL ALLYL TRISULPHIDE
  • FEMA 3253
  • 1-Allyl-3-methyltrisulfane
  • Methyl 2-propenyl trisulfide
  • Trisulfide, methyl 2-propenyl
CAS:
34135-85-8
MF:
C4H8S3
MW:
152.3
EINECS:
251-843-8
Product Categories:
  • sulfide Flavor
Mol File:
34135-85-8.mol
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Methyl allyl trisulfide Chemical Properties

Melting point:
<25 °C
Boiling point:
bp0.05 28-30°
Density 
1.157±0.06 g/cm3(Predicted)
FEMA 
3253 | ALLYL METHYL TRISULFIDE
form 
Liquid
color 
Colorless to light yellow
Odor
at 0.10 % in propylene glycol. alliaceous creamy garlic onion
Odor Type
sulfurous
JECFA Number
586
InChI
InChI=1S/C4H8S3/c1-3-4-6-7-5-2/h3H,1,4H2,2H3
InChIKey
JGMPRNFEEAJLAJ-UHFFFAOYSA-N
SMILES
S(SC)SCC=C
LogP
2.72
NIST Chemistry Reference
Trisulfide, methyl 2-propenyl(34135-85-8)

MSDS

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Methyl allyl trisulfide Usage And Synthesis

Chemical Properties

An oil-soluble component of garlic with a strong odor

Occurrence

Reported found in garlic (Allium sativum L.), onion (Allium cepa L.), chive (Allium schoenoprasum L.), nira (Allium tuberosum Rottl.), caucas (Allium victoralis L.), nobiru (Allium grayi Regal).

Uses

Methyl allyl trisulfide is a volatile organic compound, and a component of the essential oils of garlic (Allium sativum L.). Methyl allyl trisulfide shows antiviral activity against HSV-1 in African green monkey kidney cell and antioxidant activity against DPPH radical in DMSO.

in vivo

Allyl methyl trisulfide (AMS) (50-200 mg/kg, orally, daily, 30 days) has protective effect in STZ-induced hyperglycemia rats. It can lead to a significant decrease in the expression of blood glucose and pro-inflammatory markers TNF-α, IL-6, and NF-κB p65, while increasing plasma insulin levels, and has some antioxidant activity[1].

Animal Model:Male Wistar rats (170-190 g)[1]
Dosage:50, 100 and 200 mg/kg
Administration:orally in the daily morning for 30 days
Result:Enhanced body, organ weight and reduced food, water intake.
Dose-dependently decreased plasma glucose and enhanced insulin.
Attenuated the oxidative stress stimulated by STZ in hepatocytes.
Increased activity of hepatotoxicity markers AST, ALT and ALP.
Significantly downregulated the expression of pro-inflammatory proteins, cytokines (TNF-α and IL-6) and transcription factors (NF-κB p65).

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