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10496-18-1

10496-18-1 Structure

10496-18-1 Structure
IdentificationMore
[Name]

DIDECYL DISULFIDE
[CAS]

10496-18-1
[Synonyms]

DECYL DISULFIDE
DIDECYL DISULFIDE
DI-N-DECYL DISULFIDE
1-(Decyldisulfanyl)decane
Disulfide, didecyl
Di-N-Decyl
NISTC10496181
DIDECYLDISULPHIDE
Bisdecyl persulfide
Didecyl perdisulfide
Didecyl persulfide
[Molecular Formula]

C20H42S2
[MDL Number]

MFCD00039859
[Molecular Weight]

346.68
[MOL File]

10496-18-1.mol
Chemical PropertiesBack Directory
[Melting point ]

-13.99°C
[Boiling point ]

208 °C / 2mmHg
[density ]

0.89
[refractive index ]

1.4790-1.4840
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to lump to clear liquid
[color ]

White or Colorless to Light yellow
[LogP]

11.321 (est)
[CAS DataBase Reference]

10496-18-1(CAS DataBase Reference)
Safety DataBack Directory
[HS Code ]

2930.90.9250
Spectrum DetailBack Directory
[Spectrum Detail]

DIDECYL DISULFIDE(10496-18-1)MS
DIDECYL DISULFIDE(10496-18-1)1HNMR
DIDECYL DISULFIDE(10496-18-1)13CNMR
DIDECYL DISULFIDE(10496-18-1)IR1
Well-known Reagent Company Product InformationBack Directory
[TCI AMERICA]

Didecyl Disulfide,>90.0%(GC)(10496-18-1)
Hazard InformationBack Directory
[Synthesis]

1-IODODECANE

2050-77-3

DIDECYL DISULFIDE

10496-18-1

The general procedure for the synthesis of didecyl disulfide from 1-iododecane is as follows: at room temperature, Na2S-3H2O (0.291 g, 2.2 mmol) was added to a solution of PEG-200 (2 mL) containing the alkyl halide (2 mmol) and C2Cl6 or CCl4 (1.5 mmol), which had been pre-placed on a magnetic stirrer. The reaction mixture was stirred continuously until the starting halide was completely consumed (reaction time of about 30 to 150 min). Upon completion of the reaction, the reaction mixture was diluted with H2O (1 mL) and subsequently extracted with EtOAc-hexane (1:1, v/v; 4 x 2 mL). All organic extracts were combined, concentrated and purified by silica gel column chromatography. The target product didecyl disulfide was finally obtained in high yield (see Table 1).

[References]

[1] Synlett, 2015, vol. 26, # 9, p. 1185 - 1190
[2] Journal of the Iranian Chemical Society, 2013, vol. 10, # 2, p. 201 - 205
[3] New Journal of Chemistry, 2016, vol. 40, # 1, p. 89 - 92
[4] Bulletin of the Chemical Society of Japan, 2010, vol. 83, # 6, p. 698 - 702
[5] Journal of Organometallic Chemistry, 2017, vol. 833, p. 10 - 17
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