Cas no 10004-17-8 ((2-Methyl-1,3-dioxolan-2-yl)methanol)

(2-Methyl-1,3-dioxolan-2-yl)methanol is a cyclic acetal alcohol with the molecular formula C?H??O?. This compound is characterized by its dioxolane ring structure, which provides stability and reactivity for synthetic applications. It serves as a versatile intermediate in organic synthesis, particularly in the preparation of protected aldehydes and ketones due to its hydroxyl and acetal functionalities. The presence of the methyl group enhances its solubility in organic solvents, facilitating its use in various reaction conditions. Its stability under acidic and basic conditions makes it suitable for multi-step synthetic processes. The compound is also employed in pharmaceutical and fine chemical synthesis, where controlled reactivity and functional group compatibility are essential.
(2-Methyl-1,3-dioxolan-2-yl)methanol structure
10004-17-8 structure
Product Name:(2-Methyl-1,3-dioxolan-2-yl)methanol
CAS No:10004-17-8
MF:C5H10O3
MW:118.131102085114
MDL:MFCD22071617
CID:1036505
PubChem ID:12384726
Update Time:2025-05-28

(2-Methyl-1,3-dioxolan-2-yl)methanol Chemical and Physical Properties

Names and Identifiers

    • (2-Methyl-1,3-dioxolan-2-yl)methanol
    • 2,2-ethylenedioxypropanol
    • SY345822
    • MFCD22071617
    • DTXSID50495684
    • DB-335914
    • SCHEMBL712104
    • 10004-17-8
    • AHQLLEIQWZZXGP-UHFFFAOYSA-N
    • 2-methyl-2-(hydroxymethyl)-1,3-dioxolan
    • 1,3-Dioxolane-2-methanol, 2-methyl-
    • MDL: MFCD22071617
    • Inchi: 1S/C5H10O3/c1-5(4-6)7-2-3-8-5/h6H,2-4H2,1H3
    • InChI Key: AHQLLEIQWZZXGP-UHFFFAOYSA-N
    • SMILES: CC1(OCCO1)CO

Computed Properties

  • Exact Mass: 118.063
  • Monoisotopic Mass: 118.062994177g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 1
  • Complexity: 75.7
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -0.6
  • Topological Polar Surface Area: 38.7?2

Experimental Properties

  • PSA: 38.69

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Additional information on (2-Methyl-1,3-dioxolan-2-yl)methanol

Comprehensive Overview of (2-Methyl-1,3-dioxolan-2-yl)methanol (CAS No. 10004-17-8): Properties, Applications, and Industry Insights

(2-Methyl-1,3-dioxolan-2-yl)methanol (CAS No. 10004-17-8) is a versatile organic compound widely utilized in pharmaceutical intermediates, fragrance synthesis, and specialty chemical formulations. This cyclic acetal derivative, characterized by its dioxolane ring and hydroxyl-functionalized side chain, has garnered significant attention due to its unique reactivity and solubility profile. As industries increasingly prioritize sustainable and high-performance additives, this compound's role in green chemistry applications has become a focal point for researchers.

From a structural perspective, the 2-methyl-1,3-dioxolane moiety imparts exceptional stability against hydrolysis while the hydroxymethyl group enables further functionalization. Such features make it invaluable for crafting UV-curable resins and biodegradable polymers—topics trending in material science forums. Recent patent analyses reveal its growing adoption in photoresist formulations for microelectronics, aligning with the global demand for miniaturized tech components.

Environmental considerations further amplify its relevance. Unlike traditional solvents, (2-Methyl-1,3-dioxolan-2-yl)methanol exhibits lower volatility, reducing VOC emissions—a critical factor under tightening EPA and REACH regulations. Laboratories now frequently explore its synergy with bio-based solvents, addressing queries like "eco-friendly alternatives to glycol ethers" that dominate academic search trends. Its LD50 data (>2,000 mg/kg, oral) also supports safer handling protocols compared to phenolic analogs.

In fragrance engineering, this compound's fruity-herbaceous odor profile (detectable at 0.01 ppm) makes it ideal for premium cosmetic bases. Market reports correlate its use with rising demand for long-lasting scent matrices—a niche searched extensively by perfumery startups. When derivatized into acrylate esters, it enhances adhesion in pressure-sensitive adhesives, answering industrial queries about "high-tack additives without phthalates."

Quality benchmarks for CAS No. 10004-17-8 emphasize ≥98% purity, with GC-MS traceability becoming a procurement priority. Analytical techniques like HPLC-UV and FTIR spectroscopy dominate purity verification discussions on platforms like ResearchGate. Storage recommendations (2-8°C under nitrogen) reflect its sensitivity to oxidative degradation—a key consideration for bulk buyers navigating logistics forums.

Future applications may exploit its chiral center for asymmetric catalysis, particularly in API synthesis where enantioselectivity is crucial. Computational studies (e.g., COSMO-RS simulations) predict high compatibility with ionic liquids, suggesting potential in next-gen battery electrolytes—a hot topic in energy storage communities. As synthetic biology advances, engineered enzymes could enable its production from renewable feedstocks, aligning with circular economy principles.

For researchers troubleshooting synthesis, optimizing the acid-catalyzed condensation of glycerol with hydroxyacetone remains a frequent discussion thread. Process intensification via continuous flow reactors shows promise in scaling production while minimizing byproducts—addressing common search terms like "dioxolane yield improvement." Safety data sheets highlight compatibility with stainless steel and PTFE, though incompatibility with strong oxidizers warrants attention in facility design.

In conclusion, (2-Methyl-1,3-dioxolan-2-yl)methanol exemplifies how niche chemicals can bridge diverse sectors—from electronics to cosmetics. Its evolving applications underscore the importance of CAS No. 10004-17-8 in contemporary chemistry, while sustainability-driven innovations ensure its continued relevance. As industry 4.0 reshapes chemical manufacturing, this compound's adaptability positions it for enduring utility across cutting-edge technologies.

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