Enzymatic synthesis of dioctyl sebacate - ScienceDirect
2.3. Ester synthesis. Dioctyl sebacate (dioctyl decanedioate) was synthetized by esterification of sebacic acid and octanol (1-octanol and 2-octanol). The synthesis was carried out in a closed 15 mL batch reactor magnetically stirred, and coupled to a condenser in order to avoid alcohol loss.
Dioctyl sebacate
Dioctyl sebacate (also di (2-ethylhexyl) sebacate, commonly abbreviated as DOS, DEHS, and BEHS) is an organic compound which is the diester of sebacic acid and 2-ethylhexanol . It is an oily colorless liquid and is used as a plasticizer, including in the explosive C4. [3]
A Viable and Sustainable Alternative to Dioctyl Sebacate
While dioctyl sebacate (di (2-ethylhexyl) sebacate, or DOS) is a widely used plasticizer, it has become more challenging for companies to acquire sebacic acid-based plasticizers like DOS due to increasing costs, along with the uncertainty and lack of stable supply of sebacic acid.
Dioctyl sebacate | 122-62-3 - ChemicalBook
Dioctyl sebacate is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions.
Dioctyl sebacate AldrichCPR | Sigma-Aldrich
CDS000559 Dioctyl sebacate AldrichCPR Empirical Formula (Hill Notation): C26H50O4 CAS Number: 2432-87-3 Molecular Weight: 426.67 EC Number: 219-411-3 MDL number: MFCD00059269 PubChem Substance ID: 329777894 Pricing and availability is not currently available. Properties form liquid SMILES string CCCCCCCCOC (=O)CCCCCCCCC (=O)OCCCCCCCC InChI
