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Detail of "2690-08-6"

  • MSDS Download
  • CAS Number:
  • 2690-08-6
  • Name:
  • Octane, 1,1'-thiobis-

  • Superlist Name:
  • Dioctyl sulphide
  • Molecular Structure:
  • Formula:
  • C16H34S
  • Molecular Weight:
  • 258.51
  • Synonyms:
  • Octylsulfide (6CI,7CI,8CI);1-(1-Octylthio)octane;Bis(1-octyl) sulfide;Di-n-octylsulfide;Di-n-octyl thioether;Dioctyl sulfide;Dioctyl thioether;NSC 65459;
  • EINECS:
  • 220-259-5
  • Density:
  • 0.842
  • Melting Point:
  • -1°C
  • Boiling Point:
  • 332.6 °C at 760 mmHg
  • Flash Point:
  • 172.2 °C
  • Hazard Symbols:
  • Risk Codes:
  • R41   
  • Safety:
  • S26;S39    Details

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CAS No.2690-08-6 Dioctyl sulphide

Dioctyl sulfide

Supplier:Shijiazhuang Lida Chemical Co., Ltd. [ China (Mainland)]

610Integral
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Tel:86-311-85737996

Address:West of Wuji County Hebei Province China.

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Reference

Microbial desulfurization of petroleum and heavy petroleum fractions
Microbial desulfurization of petroleum and heavy petroleum fractions. 4. Anaerobic degradation of organic sulfur compounds of petroleum. Koehler, M.; Genz, I. L.; Schicht, B.; Eckart, V. (Sekt. Biol., Ernst-Moritz-Arndt-Univ. Greifswald, Greifswald 2200, Ger. Dem. Rep.). Zentralbl. Mikrobiol., 139(4), 239-47 (German) 1984. CODEN: ZEMIDI. ISSN: 0232-4393. DOCUMENT TYPE: Journal CA Section: 51 (Fossil Fuels, Derivatives, and Related Products) Section cross-reference(s): 16 The anaerobic desulfurization efficiency of a selected Desulfovibrio strain was investigated in the presence of H for a series of S-contg. model compds. Of 9 S compds., (PhCH2)2S [538-74-9] and dibenzothiophene [132-65-0] were degraded to a large extent. (Ph2CH2)2S2 [150-60-7], thianaphthenes, Bu2S [544-40-1], and dioctyl sulfide [2690-08-6] were only slightly degraded. Mercaptans were not degraded. Cell-free exts. desulfurized (PhCH2)2S, thiophene [110-02-1], and Bu2S. The degree of desulfurization is related to growth conditions and hydrogenase activity of the cells. The degrdn. products of (PhCH2)2S(H2S, PhMe [108-88-3], and PhCH2SH [538-74-9]) refer to different mechanisms of reductive splitting of S-C bonds.
Relations between the chemical reactivity of extreme-pressure additives and their lubricating properties
Relations between the chemical reactivity of extreme-pressure additives and their lubricating properties. Kramarz, J.; Chmura, M. (Fac. Chem., Tech. Univ. Krakow, Krakow, Pol.). Schmierungstechnik, 15(7), 209-12 (German) 1984. CODEN: SHRGAC. ISSN: 0371-0157. DOCUMENT TYPE: Journal CA Section: 51 (Fossil Fuels, Derivatives, and Related Products) Lubricating oil extreme-pressure additives were tested by heating the additive-contg. white oil base by an immersed elec.-heated wire and measuring the thickness of the formed layer. Additives tested were chloro paraffins, org. sulfides (R2S, R = PhCH2 [538-74-9], octyl [2690-08-6], and Ph [139-66-2]), org. disulfides (RSSR, R = PhCH2 [150-60-7], octyl [822-27-5], and Ph [882-33-7]), PhCH2Cl [100-44-7], and mixts. of PhCH2SSCH2Ph with chloroparaffins or PhCH2Cl. Activation energies for layer formation are 88.7-93.7 kJ/mol for the disulfides, 302.1-315.1 kJ/mol for the sulfides, 53.5 kJ/mol for PhCH2Cl, and 139.7 kJ/mol for the chloroparaffins. In addn., the additives were tested in a 4-ball std. test. Linear correlations were obtained between lubrication properties and chem. reactivity for the S compds. and the Cl compds. but not for the mixts.
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