33922-73-5

Basic information

• Product Name: 2-PROPENYL PROPYL TRISULFIDE
• Synonyms: ALLYL PROPYL TRISULFIDE;ALLYL PROPYL TRISULPHIDE;ALLYL N-PROPYL TRISULFIDE;2-PROPENYL PROPYL TRISULFIDE;Trisulfide, 2-propenyl propyl;Propylallyltrisulfide
• CAS NO: 33922-73-5
• Molecular Formula: C6H12S3
• Molecular Weight: 180.35
• Product Categories: sulfide Flavor
• Mol File: 33922-73-5.mol

Chemical Properties

• Boiling Point: 243.3 °C at 760 mmHg
• Flash Point: 97.1 °C
• Appearance: /
• Density: 1.095 g/cm³
• CAS DataBase Reference: 2-PROPENYL PROPYL TRISULFIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PROPENYL PROPYL TRISULFIDE(33922-73-5)
• EPA Substance Registry System: 2-PROPENYL PROPYL TRISULFIDE(33922-73-5)

Safety Data

• Hazardous Substances Data: 33922-73-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2-PROPENYL PROPYL TRISULFIDE is used as an additive for garlic oil to enhance the bioavailability of coenzyme-10. This application is particularly relevant in the pharmaceutical industry, where improving the absorption and effectiveness of essential nutrients and supplements is crucial for overall health and well-being.
Application Reason:
The use of 2-PROPENYL PROPYL TRISULFIDE in the pharmaceutical industry is primarily due to its ability to increase the bioavailability of coenzyme-10 when used alongside garlic oil. This enhancement in bioavailability can lead to improved health outcomes and more effective treatment options for various conditions.

Upstream product

• 5824-50-0 Acetyl-aethyldisulfid 
• 52713-51-6 toluene-4-thiosulfonic acid S-2-propen-1-yl ester 

Relevant articles and documents

Unsymmetrical Organotrisulfide Formation via Low-Temperature Disulfanyl Anion Transfer to an Organothiosulfonate

New methodology is presented for the formation of unsymmetrical organotrisulfides in a high yield and purity, relatively free of polysulfide byproducts. The highlight of the method is the low-temperature (-78 °C) deprotection of a disulfanyl acetate with sodium methoxide in THF to form a disulfanyl anion, which reacts rapidly in situ with an organothiosulfonate (S-aryl or S-alkyl) within 30 seconds followed by quenching. The discovery of these new reaction conditions together with the relative greenness of the chemistry overall makes for an efficient protocol, from which a range of organotrisulfides covering aliphatic, aromatic, as well as cysteine and sugar groups can be accessed in a high yield and purity.

Antiviral composition derived from allium CEPA and therapeutic use thereof

Novel medicinal extracts derived from Allium species, preferablyAllium cepaare provided. These extracts have broad medicinal properties, especially for treatment of AIDS and other viral infections.