Date published: 2026-4-25

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2,2-Dimethyl-1,3-dioxolane (CAS 2916-31-6)

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Alternate Names:
Acetone ethylene acetal
CAS Number:
2916-31-6
Molecular Weight:
102.13
Molecular Formula:
C5H10O2
Supplemental Information:
This is as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2,2-Dimethyl-1,3-dioxolane is an organic compound with applications in various research domains. Its dioxolane ring structure makes it a valuable solvent in organic synthesis, where it is used to dissolve both polar and non-polar substances, allowing for a wide range of chemical reactions. In the field of green chemistry, it is studied for its potential as a bio-based solvent, aiming to replace more toxic or environmentally harmful alternatives. Additionally, this compound is investigated for its use as a stabilizing agent in the production of chlorinated solvents, where it can help in reducing the formation of acid during storage. Researchers also examine the ring-opening polymerization of 2,2-dimethyl-1,3-dioxolane as a route to produce polyacetals, which are important in creating biodegradable plastics.


2,2-Dimethyl-1,3-dioxolane (CAS 2916-31-6) References

  1. Synthesis, swelling behavior, and biocompatibility of novel physically cross-linked polyurethane-block-poly(glycerol methacrylate) hydrogels.  |  Mequanint, K., et al. 2006. Biomacromolecules. 7: 883-91. PMID: 16529427
  2. Rapid analysis of tile industry gaseous emissions by ion mobility spectrometry and comparison with solid phase micro-extraction/gas chromatography/mass spectrometry.  |  Pozzi, R., et al. 2006. J Environ Monit. 8: 1219-26. PMID: 17133278
  3. Pyrene magic: chiroptical enciphering and deciphering 1,3-dioxolane bearing two wirepullings to drive two remote pyrenes.  |  Amako, T., et al. 2015. Chem Commun (Camb). 51: 8237-40. PMID: 25820177
  4. Application of acetone acetals as water scavengers and derivatization agents prior to the gas chromatographic analysis of polar residual solvents in aqueous samples.  |  van Boxtel, N., et al. 2015. J Chromatogr A. 1425: 62-72. PMID: 26614172
  5. Synthesis, structure and pyrolysis of stabilised phosphonium ylides containing saturated oxygen heterocycles.  |  Aitken, RA., et al. 2016. Org Biomol Chem. 14: 1794-804. PMID: 26751733
  6. Design, synthesis and evaluation of 2,2-dimethyl-1,3-dioxolane derivatives as human rhinovirus 3C protease inhibitors.  |  Zhang, Q., et al. 2017. Bioorg Med Chem Lett. 27: 4061-4065. PMID: 28778471
  7. Chemical constituents of Antidesma bunius aerial parts and the anti-AGEs activity of selected compounds.  |  Nguyen-Ngoc, H., et al. 2022. Phytochemistry. 202: 113300. PMID: 35798090
  8. Potential Role of Low-Molecular-Weight Dioxolanes as Adjuvants for Glyphosate-Based Herbicides Using Photosystem II as an Early Post-Treatment Determinant.  |  Szwajczak, E., et al. 2023. Cells. 12: PMID: 36899913

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2,2-Dimethyl-1,3-dioxolane, 25 g

sc-238228
25 g
$117.00