Description

Dimethyl 2,5-Dioxahexanedioate (CAS: 88754-66-9) is a high-purity organic compound with the molecular formula C₆H₁₀O₆. This versatile ester derivative is widely utilized in pharmaceutical synthesis, polymer chemistry, and specialty chemical applications due to its unique bifunctional carbonate structure. The compound appears as a clear to pale yellow liquid (or low-melting solid) with excellent solubility in common organic solvents. Our product is rigorously tested to ensure ≥98% purity (GC) and is supplied with comprehensive analytical documentation including HPLC, GC-MS, and NMR spectra. Available in research quantities (100mg-10g) or bulk scale (100g-1kg+), this chemical is packaged under inert atmosphere to ensure stability and longevity. Shelf life is typically 24 months when stored at 2-8°C in the original sealed container.

Properties

• CAS Number: 88754-66-9
• Complexity: 136
• IUPAC Name: 2-methoxycarbonyloxyethyl methyl carbonate
• InChI: InChI=1S/C6H10O6/c1-9-5(7)11-3-4-12-6(8)10-2/h3-4H2,1-2H3
• InChI Key: DOMLQXFMDFZAAL-UHFFFAOYSA-N
• Exact Mass: 178.04773803
• Molecular Formula: C6H10O6
• Molecular Weight: 178.14
• SMILES: COC(=O)OCCOC(=O)OC
• Topological: 71.1
• Monoisotopic Mass: 178.04773803
• Synonyms: 88754-66-9, 2,5-Dioxahexanedioic Acid Dimethyl Ester, Dimethyl 2,5-Dioxahexanedioate, 2-methoxycarbonyloxyethyl methyl carbonate, ethane-1,2-diyl dimethyl dicarbonate, 2,5-DIOXAHEXANEDIOICACIDDIMETHYLESTER, NSC97193, MFCD00085447, SCHEMBL47896, DTXSID20294585, NDA75466, NSC-97193, AKOS015840251, Ethane-1,2-diyl dimethyl bis(carbonate), BS-44080, CS-0330558, D2455, ETHYLENE GLYCOL BIS-(METHYL CARBONATE), D90066

Dimethyl 2,5-Dioxahexanedioate serves as a valuable building block in organic synthesis, particularly for creating carbonate-linked polymer backbones. Its bifunctional nature makes it ideal for step-growth polymerization reactions to produce polycarbonates with tailored properties. The compound has shown utility as a protecting group reagent in nucleoside chemistry and as a precursor for electrolyte additives in advanced battery systems. Researchers also employ this diester in the development of prodrug formulations due to its hydrolytic cleavage characteristics under physiological conditions.

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