57500-00-2

Basic information

• Product Name: Methyl furfuryl disulfide
• Synonyms: 2-[(Methyldisulfanyl)methyl]furan;2-[(methyldithio)methyl]-fura;2-[(methyldithio)methyl]furan;2-furfurylmethyl-disulphide;Furan, 2-[(methyldithio)methyl]-;METHYL FURFURYL DISULFIDE;METHYL FURFURYL DISULPHIDE;LABOTEST-BB LT00159945
• CAS NO: 57500-00-2
• Molecular Formula: C₆H₈OS₂
• Molecular Weight: 160.26
• EINECS: 260-773-7
• Product Categories: sulfide Flavor
• Mol File: 57500-00-2.mol

Chemical Properties

• Boiling Point: 60-61 °C0.8 mm Hg
• Flash Point: 194 °F
• Appearance: /
• Density: 1.162 g/mL at 25 °C
• Vapor Pressure: 0.066mmHg at 25°C
• Refractive Index: n20/D 1.568
• Storage Temp.: Store below +30°C.
• CAS DataBase Reference: Methyl furfuryl disulfide(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl furfuryl disulfide(57500-00-2)
• EPA Substance Registry System: Methyl furfuryl disulfide(57500-00-2)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• RIDADR: UN 3334
• WGK Germany: 3
• Hazardous Substances Data: 57500-00-2(Hazardous Substances Data)

Usage

Uses

Used in Flavor Industry:
Methyl furfuryl disulfide is used as a flavoring agent for its characteristic berry, fruity, and vegetable flavor. It adds a unique taste to the products, enhancing their overall flavor profile.
Used in Fragrance Industry:
Methyl furfuryl disulfide is used as a component in the creation of various fragrances due to its pleasant and distinctive odor. It contributes to the development of scents that are reminiscent of berries, fruits, and vegetables, making it a valuable addition to the fragrance industry.
Used in Food Industry:
Methyl furfuryl disulfide is used as an additive in the food industry to impart a specific flavor to various products. Its natural occurrence in certain food items makes it a suitable choice for enhancing the taste and aroma of different dishes and food products.
Used in Cosmetic Industry:
Methyl furfuryl disulfide can be used in the cosmetic industry for its pleasant odor, potentially being incorporated into products like perfumes, body lotions, and other personal care items to provide a fresh and appealing scent.

InChI:InChI=1/C6H8OS2/c1-8-9-5-6-3-2-4-7-6/h2-4H,5H2,1H3

Upstream product

• 98-02-2 2-thiolomethyl-furan 
• 118087-46-0 2-methylpropanedithioperoxy acid methyl ester 
• 4437-20-1 furfuryl disulfide 
• 624-92-0 Dimethyldisulphide 
• 98-00-0 (2-furyl)methyl alcohol 
• 74-88-4 methyl iodide 

Downstream Products

• 3467-79-6 1,4-bis(methylmercapto)-2,3,5,6-tetrafluorobenzene 

Relevant articles and documents

NFSI-catalyzed S[sbnd]S bond exchange reaction for the synthesis of unsymmetrical disulfides

The metal-free S[sbnd]S bond exchange reaction of symmetrical disulfides catalyzed by NFSI is described. This novel protocol provides a facile and efficient approach to accessing important unsymmetrical disulfides. Furthermore, this strategy could also be utilized in the late-stage functionalization of amino acids, drugs, and natural products. The broad substrate scope, good functional group tolerance and easy accessibility of catalyst indicate that this strategy affords a green and practical complementary method to various unsymmetrical disulfides.

Convenient Unsymmetrical Disulfane Synthesis: Basic Zeolite-Catalyzed Thiol-Disulfane Exchange Reaction

Convenient catalytic synthetic methods for the preparation of unsymmetrical disulfanes are described. Na-exchanged X type zeolite (Na-X), commercially available as MS-13X, effectively catalyzes thiol-disulfane exchange reactions with 1.0 equivalent of thi

Potassium fluoride on alumina: A convenient synthesis of O-alkyl methyldithiocarbonates. Pyrolysis of O-benzyl-S-methyldithiocarbonates

Xanthates were easily prepared by adsorption of alcohol on KF-Al2O3 followed by treatment of carbon disulfide and iodomethane at room temperature. Pyrolysis of benzyl xanthate affords to a complex mixture of products. A radical process was proposed to explain the nature of products obtained.

The Reaction of Ph3P+SR with Thiols: A Simple, Efficient Synthesis of Unsymmetrical Disulphides

Reaction of Ph3P+SRClO4-, prepared electrochemically from RSSR and Ph3P, with thiols in n-hexane at room temperature gave unsymmetrical disulphides in excellent yields with recovery of Ph3P.