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Dibenzyl disulfide

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Identification
Molecular formula
C14H14S2
CAS number
150-60-7
IUPAC name
(benzyldisulfanyl)methylbenzene
State
State

At room temperature, dibenzyl disulfide is typically a solid. It may appear as a flaky or powdered solid and does not volatilize easily under normal conditions.

Melting point (Celsius)
71.00
Melting point (Kelvin)
344.00
Boiling point (Celsius)
348.00
Boiling point (Kelvin)
621.00
General information
Molecular weight
246.37g/mol
Molar mass
246.3740g/mol
Density
1.2350g/cm3
Appearence

Dibenzyl disulfide is a colorless to pale yellow solid. It often occurs as crystalline flakes or powders, depending on its purity.

Comment on solubility

Solubility of (benzyldisulfanyl)methylbenzene

(benzyldisulfanyl)methylbenzene, also known as a thioether compound, exhibits intriguing solubility characteristics that are worth noting. The solubility of organic compounds is influenced by various factors, and in the case of this compound, several elements come into play:

  • Polarity: (benzyldisulfanyl)methylbenzene is a relatively nonpolar compound due to its aromatic structure and sulfur-containing moiety, which can limit its solubility in polar solvents.
  • Solvent Compatibility: It is more soluble in nonpolar solvents such as benzene or toluene, while its solubility in water is expected to be quite low.
  • Functional Groups: The presence of disulfide linkages may interact with specific solvents but does not significantly enhance solubility in aqueous environments.

In summary, the solubility of (benzyldisulfanyl)methylbenzene can be succinctly encapsulated as follows: it is more soluble in nonpolar organic solvents and exhibits limited solubility in polar solvents, especially water. As with many organic compounds, the balance of polar and nonpolar characteristics plays a crucial role in determining solubility behavior.

Interesting facts

Interesting Facts about (Benzyldisulfanyl)methylbenzene

(Benzyldisulfanyl)methylbenzene, also known as benzyl thiodipropionate, includes a sulfur-containing moiety that gives it unique properties and applications. This compound belongs to the class of thioethers and is particularly interesting due to its potential in various fields:

  • Biological Relevance: The presence of sulfur in its structure has been linked to significant biological activities, such as antioxidant and anticancer properties. Compounds like this can play a role in protecting cells from oxidative stress.
  • Industrial Applications: (Benzyldisulfanyl)methylbenzene is utilized in the synthesis of various organic compounds, making it a valuable intermediate in the chemical industry.
  • Flavor and Fragrance: Due to its aromatic nature, this compound is studied for its potential use in the formulation of fragrances and flavoring agents, allowing for a more extensive olfactory range in products.
  • Synthetic Utility: This compound can serve as a starting material or reactant in organic synthesis, particularly in the preparation of new materials with specialized properties.
  • Environmental Considerations: As research continues into the environmental impact of chemical compounds, the sustainability and biodegradability of (benzyldisulfanyl)methylbenzene become topics of interest for chemists aiming to develop greener processes.

Overall, the study of (benzyldisulfanyl)methylbenzene reveals not only its chemical and physical properties but also its implications in various scientific disciplines. As stated in a recent study, "Understanding the role of sulfur-containing compounds in biological systems remains a frontier of research in chemistry."

By exploring the multifaceted applications of this compound, researchers can contribute to advancements in medicine, industry, and environmental science.

Synonyms
Dibenzyl disulfide
150-60-7
Benzyl disulfide
Disulfide, bis(phenylmethyl)
Dibenzyl disulphide
1,2-dibenzyldisulfane
Dibenzyldisulfid
Benzyl bisulfide
Di(phenylmethyl)disulfide
(benzyldisulfanyl)methylbenzene
Bis(phenylmethyl) disulfide
DISULFIDE, DIBENZYL
Benzyldisulfide
alpha-(Benzyldithio)toluene
1,4-Diphenyl-2,3-dithiabutane
Di(phenylmethyl) disulfide
Dibenzyldisulfide
Diphenylmethyl disulfide
Dibenzyldisulfid [Czech]
1,4-Diphenyl-2,3-dithiobutane
[(Benzyldisulfanyl)methyl]benzene
NSC 6841
.alpha.-(Benzyldithio)toluene
FEMA No. 3617
CCRIS 6924
NSC 677465
EINECS 205-764-0
ghl.PD_Mitscher_leg0.312
BDS
UNII-BG7680605N
CHEBI:72752
4,4'-Biphenyldiglyoxal disodium bisulfite
1,1'-(disulfanediyldimethanediyl)dibenzene
Benzyl disulfide, 8CI
NSC-6841
Benzyl disulfide (8CI)
MFCD00004783
1,1'-[dithiobis(methylene)]dibenzene
NSC-677465
DAILUBE S 700
benzyldisulfanyl-methyl-benzene
BENZYL DISULFIDE [FHFI]
DIBENZYL DISULFIDE [MI]
DTXSID6059738
FEMA 3617
BENZYL DISULFIDE [USP-RS]
Bis(phenylmethyl) disulfide, 9CI
NSC677465
BG7680605N
BENZYL DISULFIDE (USP-RS)
benzyl disulphide
Benzyl bisulphide
dibenzyldisulphide
dibenzyl-disulfide
1,3-dithiabutane
a-(Benzyldithio)toluene
alpha(Benzyldithio)toluene
Dibenzyl disulfide, 98%
Di(phenylmethyl) disulphide
bis(phenylmethyl) disulphide
WLN: R1SS1R
1,4Diphenyl2,3dithiabutane
1,4Diphenyl2,3dithiobutane
alpha-(Benzyldithio))toluene
Benzyl disulfide, 98%, FG
Dibenzyl disulfide (Standard)
SCHEMBL160895
CHEMBL121047
DTXCID0034859
NSC6841
HY-W009516R
[(Benzyldisulfanyl)methyl]benzene #
STK831913
AKOS005177808
CS-W010232
Dibenzyl disulfide, analytical standard
HY-W009516
SY008111
DB-003625
B0417
NS00020151
EN300-16500
D77707
Dibenzyl disulfide 2 microg/mL in Transformer Oil
Dibenzyl disulfide 10 microg/mL in Transformer Oil
Q27140119
Z55949860
Benzyl disulfide, United States Pharmacopeia (USP) Reference Standard