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Pentasulfide, didodecyl, also known as bis(dodecyl) pentasulfide, is an organosulfur compound with the chemical formula C24H50S5. It is a colorless to pale yellow liquid with a faint, characteristic odor. Pentasulfide, didodecyl is primarily used as a vulcanizing agent and accelerator in the rubber industry, particularly for natural rubber and certain synthetic rubbers. It enhances the elasticity, strength, and durability of rubber products by promoting the formation of cross-links between polymer chains during the vulcanization process. Pentasulfide, didodecyl, is also known for its ability to improve the resistance of rubber to heat, aging, and mechanical stress. Due to its effectiveness and versatility, it is widely employed in various applications, including tires, hoses, seals, and other rubber goods.

4089-79-6

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4089-79-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4089-79-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,8 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4089-79:
(6*4)+(5*0)+(4*8)+(3*9)+(2*7)+(1*9)=106
106 % 10 = 6
So 4089-79-6 is a valid CAS Registry Number.

4089-79-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(dodecylpentasulfanyl)dodecane

1.2 Other means of identification

Product number -
Other names didodecyl-pentasulfane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4089-79-6 SDS

4089-79-6Downstream Products

4089-79-6Relevant academic research and scientific papers

Electrochemical Synthesis of Organic Polysulfides from Disulfides by Sulfur Insertion from S8 and an Unexpected Solvent Effect on the Product Distribution

F?hrmann, Jan,Hilt, Gerhard

, p. 11141 - 11149 (2021)

An electrochemical synthesis of organic polysulfides through sulfur insertion from elemental sulfur to disulfides or thiols is introduced. The highly economic, low-sensitive and low-priced reaction gives a mixture of polysulfides, whose distribution can be influenced by the addition of different amounts of carbon disulfide as co-solvent. To describe the variable distribution function of the polysulfides, a novel parameter, the “absorbance average sulfur amount in polysulfides” (SAP) was introduced and defined on the basis of the “number average molar mass” used in polymer chemistry. Various organic polysulfides were synthesized with variable volume fractions of carbon disulfide, and the yield of each polysulfide was determined by quantitative 13C NMR. Moreover, by using two symmetrical disulfides or a disulfide and a thiol as starting materials, a mixture of symmetrical and asymmetrical polysulfides could be obtained.

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