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Atomfair 1,3-Dimethoxypropane C5H12O2
Description 1,3-Dimethoxypropane (CAS No. 17081-21-9) is a high-purity organic compound with the molecular formula C5H12O2, widely utilized in research and industrial applications. This clear, colorless liquid is characterized by its ether-like odor and excellent solubility in common organic solvents, making it a versatile reagent in synthetic chemistry. With an IUPAC name of 1,3-dimethoxypropane , it is also known by synonyms such as Trimethylene glycol dimethyl ether and CH3O(CH2)3OCH3. Its stability and reactivity under controlled conditions make it ideal for use as a solvent, protecting group agent, or intermediate in organic synthesis. Packaged under inert gas to ensure longevity, our product…
Description
Description
1,3-Dimethoxypropane (CAS No. 17081-21-9) is a high-purity organic compound with the molecular formula C5H12O2, widely utilized in research and industrial applications. This clear, colorless liquid is characterized by its ether-like odor and excellent solubility in common organic solvents, making it a versatile reagent in synthetic chemistry. With an IUPAC name of 1,3-dimethoxypropane, it is also known by synonyms such as Trimethylene glycol dimethyl ether and CH3O(CH2)3OCH3. Its stability and reactivity under controlled conditions make it ideal for use as a solvent, protecting group agent, or intermediate in organic synthesis. Packaged under inert gas to ensure longevity, our product meets stringent purity standards (>98%) and is supplied in amber glass bottles to prevent degradation.
- CAS No: 17081-21-9
- Molecular Formula: C5H12O2
- Molecular Weight: 104.15
- Exact Mass: 104.083729621
- Monoisotopic Mass: 104.083729621
- IUPAC Name: 1,3-dimethoxypropane
- SMILES: COCCCOC
- Synonyms: 1,3-Dimethoxypropane, Propane, 1,3-dimethoxy-, Trimethylene glycol dimethyl ether, CH3O(CH2)3OCH3, DTXSID40168951
Application
1,3-Dimethoxypropane serves as a key solvent in Grignard reactions and other organometallic syntheses due to its ability to stabilize reactive intermediates. It is also employed as a protecting group for diols in carbohydrate chemistry, enabling selective functionalization. Additionally, this compound finds use in electrolyte formulations for lithium-ion batteries, where its low viscosity enhances ion mobility.
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