1,1,2-Trimethoxyethane

GTC-001

Ethers

1,1,2-Trimethoxyethane

CAS No.
24332-20-5
Catalogue ID
GTC-001

1,1,2-Trimethoxyethane, CAS 24332-20-5. Source-derived identification, physical data and applications are provided for catalogue reference; request the current specification, COA and SDS for the required grade.

Catalogue aliases / related identifiers

Methoxyacetaldehyde dimethyl acetal; 2,2-Dimethoxyethyl methyl ether; Ethane, 1,1,2-trimethoxy-; 2-Methoxy-1,1-dimethoxyethane; 1,1,2-Trimethoxy ethane; Methoxyacetaldehyde dimethylacetal

Supplied catalogue source: GTC-001 · Page 101

Reference data — confirm before ordering or use

The information below is a structured migration from the supplied catalogue snapshot. It is not a current product specification, COA or SDS. Confirm the actual supplier, grade, batch documents, classification, packing and destination requirements for your enquiry.

1,1,2-Trimethoxyethane (CAS 24332-20-5) is a stable acetal that serves as a protected form of methoxyacetaldehyde in organic synthesis. It allows controlled release of the reactive aldehyde functionality under acidic conditions while remaining stable during handling and storage.


Basic Information

CAS No.24332-20-5
EC No.Not available
Linear FormulaC5H12O3
Molecular Weight120.15
AppearanceColorless to almost colorless clear liquid
Melting PointNot available (typical reference)
Boiling point126 °C (lit.)
Density0.932 g/mL at 25 °C (lit.)
SolubilitySoluble in common organic solvents
Storage ConditionsStore in a tightly closed container in a cool, dry place. Keep away from heat and ignition sources.
Chemical StructureMolecular Structure of 1,1,2-Trimethoxyethane

Key Applications

  • Protected aldehyde intermediate: 1,1,2-Trimethoxyethane functions as a stable acetal-protected form of methoxyacetaldehyde, enabling controlled introduction of aldehyde functionality in multi-step organic synthesis. It is widely used in Acetals and Protected Carbonyl Ethers for Organic Synthesis, where masked carbonyl groups improve reaction selectivity and stability.

  • Acetal chemistry and protection strategies: This compound is applied in protecting group chemistry, allowing reversible masking of aldehyde functionality during complex transformations. Such applications are part of the acetal and protected carbonyl ether application category.

  • Fine chemical intermediate: Employed in the synthesis of specialty chemicals and pharmaceutical intermediates requiring controlled release of aldehyde functionality under defined reaction conditions.

  • Functional molecule construction: Facilitates the assembly of complex molecules through acetal-based strategies, supporting the design of advanced intermediates with improved stability and reactivity control.

  • Laboratory research: Widely used in research for synthetic methodology development, particularly in acetal chemistry, carbonyl protection strategies, and stepwise functional group transformations.

  • Process development: Supports route optimization and scale-up in processes requiring stable acetal intermediates and controlled deprotection steps in organic synthesis.

1,1,2-Trimethoxyethane belongs to the Acetals and Protected Carbonyl Ethers application category and is part of our broader portfolio of Ethers for Pharmaceutical Intermediates & Specialty Synthesis, covering acetal derivatives, protected aldehydes, and ether-based intermediates for API and fine chemical synthesis.


  • Flexible global supply: Established logistics networks ensure stable international supply from laboratory to bulk scale for fine chemical customers worldwide.

  • SDS and COA support: Complete SDS, COA, and technical documentation available upon request to facilitate quality review and international procurement.

  • Packaging and technical service: Flexible packaging in 25L/200L HDPE drum, backed by responsive technical assistance for application support.

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