Bis(2-ethylhexyl) 2,2'-thiobisacetate

Base Information

• Chemical Name: Bis(2-ethylhexyl) 2,2'-thiobisacetate
• CAS No.: 24293-43-4
• Deprecated CAS: 120860-55-1
• Molecular Formula: C20H38 O4 S
• Molecular Weight: 374.585
• Hs Code.: 2930909090
• European Community (EC) Number: 246-131-9
• DSSTox Substance ID: DTXSID10884898
• Nikkaji Number: J287.205F
• Mol file: 24293-43-4.mol

Synonyms:24293-43-4;Bis(2-ethylhexyl) 2,2'-thiobisacetate;Vulkanol 90;2-Ethylhexyl thiodiglycolate;Bis(2-ethylhexyl) thiodiglycolate;2-ethylhexyl 2-[2-(2-ethylhexoxy)-2-oxoethyl]sulfanylacetate;DI-2-ETHYLHEXYL THIODIGLYCOLATE;Bis(2-ethylhexyl) thiodiacetate;EINECS 246-131-9;Acetic acid, 2,2'-thiobis-, 1,1'-bis(2-ethylhexyl) ester;BRN 1804225;Acetic acid, 2,2'-thiobis-, bis(2-ethylhexyl) ester;Acetic acid, thiodi-, bis(2-ethylhexyl) ester;EC 246-131-9;4-03-00-00622 (Beilstein Handbook Reference);SCHEMBL5930242;DTXSID10884898;DI-2-ETHYLHEXYLTHIODIGLYCOLATE;bis(2-ethylhexyl) 2,2'-thiodiacetate;bis(2-ethylhexyloxycarbonylmethyl) sulfide;2,2'-Thiodiacetic acid bis(2-ethylhexyl) ester;W-110589

Chemical Property of Bis(2-ethylhexyl) 2,2'-thiobisacetate

Chemical Property:

• Vapor Pressure: 0Pa at 25℃
• Boiling Point: 438.6oC at 760 mmHg
• Flash Point: 193.2oC
• PSA: 77.90000
• Density: 0.984g/cm3
• LogP: 5.23880
• Water Solubility.: 80μg/L at 20℃
• XLogP3: 7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 18
• Exact Mass: 374.24908086
• Heavy Atom Count: 25
• Complexity: 315

Purity/Quality:

99.9% ^*data from raw suppliers

DI-2-ETHYLHEXYL THIODIGLYCOLATE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCC(CC)COC(=O)CSCC(=O)OCC(CC)CCCC

Technology Process of Bis(2-ethylhexyl) 2,2'-thiobisacetate

There total 2 articles about Bis(2-ethylhexyl) 2,2'-thiobisacetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

2-Ethylhexyl alcohol (104-76-7) + thiodiacetic acid (123-93-3) → 3-thia-glutaric acid bis-(2-ethyl-hexyl ester) (24293-43-4)

Guidance literature:

With sulfuric acid; benzene;

Reference yield:

2-ethylhexyl monochloroacetate (5345-58-4) → 3-thia-glutaric acid bis-(2-ethyl-hexyl ester) (24293-43-4)

Guidance literature:

With sodium sulfide; acetone; zuletzt bei Siedetemperatur;

upstream raw materials:

2-Ethylhexyl alcohol

thiodiacetic acid

2-ethylhexyl monochloroacetate