Dibenzyl disulfide
Dibenzyl disulfide
  • CAS No.:150-60-7
Other grades of this product :
Dibenzyl disulfide Basic information
Product Name:Dibenzyl disulfide
Synonyms:BENZYL DISULFIDE;AURORA KA-6695;DIBENZYL DISULFIDE;DIBENZYL DISULPHIDE;FEMA 3617;LABOTEST-BB LT00771553;[(Benzyldisulfanyl)methyl]benzene;1,4-Diphenyl-2,3-dithiabutane
CAS:150-60-7
MF:C14H14S2
MW:246.39
EINECS:205-764-0
Product Categories:sulfide Flavor;Aromatics;sulfide Flavor;Sulfur & Selenium Compounds;corrosion inhibitors, fragrance compounds, high-pressure lubricant additives and other organic compounds.lubricant additives
Mol File:150-60-7.mol
Dibenzyl disulfide Chemical Properties
Melting point 69-72 °C (lit.)
Boiling point 210-216°C 18mm
density 1.3
refractive index 1.6210 (estimate)
FEMA 3617 | BENZYL DISULFIDE
Fp 150°C
storage temp. 2-8°C
solubility Chloroform (Slightly), Ethyl Acetate (Slightly)
form neat
color White
JECFA Number579
Merck 14,3013
BRN 1110443
CAS DataBase Reference150-60-7(CAS DataBase Reference)
NIST Chemistry ReferenceBenzyl disulfide(150-60-7)
EPA Substance Registry SystemDisulfide, bis(phenylmethyl) (150-60-7)
Safety Information
Hazard Codes Xi
Risk Statements 43
Safety Statements 22-36/37-37-24
WGK Germany 2
RTECS JO1750000
TSCA Yes
HS Code 29309090
MSDS Information
ProviderLanguage
Benzyl disulfide English
SigmaAldrich English
ALFA English
Dibenzyl disulfide Usage And Synthesis
Chemical PropertiesBenzyl disulfide is a pale yellow leafy or small leafy crystals that has a powerful, burnt-caramel odor; irritating when concentrated. Boiling point >270°C(decomposition). Several insoluble in water, soluble in hot ethanol and ether.
UsesDibenzyl disulfide has been used in lubricating oil formulations to improve thermal and aging resistance of the oil. It is used an antioxidant in rubber compounding, stabilizer for petroleum fractions, additive to silicone oils. The soly in oils is increased by the presence of benzyl alcohol.
PreparationDibenzyl disulfide is synthesized from benzyl chloride and Na2S2; also from benzyl mercaptan via oxidation.Md. Tajbakhsh et al. (2004) synthesized disulfide from thiols by oxidation with 2,6- DCPCC in acetonitirle at room temperature. For synthesis of DBDS, they used benzyl mercaptan. In 8 min, 96% yield was obtained.Vivek Polshettiwar et al. (2003) obtained disulfide from reaction of alkyl halide with reagent (C6H5CH2N(Et)3)6Mo7S24 in presence of CHCl3 at room temperature. Pure disulfide was obtained by purification by column chromatography method on silica gel. 89% yield was obtained.
ApplicationDibenzyl Disulfide (DBDS) is one of several sulfur compounds known to cause copper corrosion in transformers under certain circumstances. Originating from Petiveria alliacea L. This compound along with the other sulfur-containing compound found in this plant display antibacterial and antifungal activity.
DefinitionChEBI: Dibenzyl disulfide is an organic disulfide that results from the formal oxidative dimerisation of benzyl thiol. It has a role as a metabolite. It is an organic disulfide and an organic aromatic compound.
Synthesis Reference(s)The Journal of Organic Chemistry, 54, p. 2998, 1989 DOI: 10.1021/jo00274a002Synthetic Communications, 22, p. 3277, 1992 DOI: 10.1080/00397919208021143Tetrahedron Letters, 31, p. 5007, 1990 DOI: 10.1016/S0040-4039(00)97790-6
General DescriptionDibenzyl Disulfide (DBDS) also called Benzyl disulfide is an aromatic disulfide with molecular formula C14H14S2. It has a structural unit, which consists of a linked pair of sulfur atoms. It is insoluble in water whereas soluble in hot methanol, benzene, ether and hot ethanol. Large disulfides-linked agglomerates are rifely found in proteins and many other biologically active molecules.
Purification MethodsCrystallise the disulfide from EtOH (m 77o), pet ether or CS2 (m 72o) or distil it. The AgNO3 complex has m 103o. [Beilstein 6 H 465, 6 I 229, 6 II 437, 6 III 1635, 6 IV 2760.]
Dibenzyl disulfide Preparation Products And Raw materials
Raw materialsBenzyl chloride-->Benzyl mercaptan
Preparation Products1-(Benzylthio)acetone-->ETHYL METHYL DISULFIDE

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