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2-Methoxyethyl acetate (CAS 110-49-6)

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Alternate Names:
1-Acetoxy-2-methoxyethane; Ethylene glycol monomethyl ether acetate
Application:
2-Methoxyethyl acetate is a solvent and yeast inducing aneuploidy agent
CAS Number:
110-49-6
Purity:
98%
Molecular Weight:
118.13
Molecular Formula:
C5H10O3
Supplemental Information:
This is classified 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-Methoxyethyl acetate, also known as methyl glycol acetate, is an organic compound categorized as an ester. It is derived from the esterification of acetic acid with 2-methoxyethanol. This chemical is characterized by its clear, colorless appearance and a mild, pleasant odor, combining properties of ethers and esters in one molecule. It is relatively soluble in water and highly soluble in most organic solvents, which makes it extremely useful in various industrial and research applications, particularly as a high-performance solvent. In research environments, 2-Methoxyethyl acetate is valued for its excellent solvent properties, particularly in the application of coatings and inks where it effectively dissolves resins, polymers, and other additives to create uniform and smooth applications without premature evaporation. Its solvent capabilities are also exploited in the cleaning of electronic components where precision and minimal residue are crucial. Further, in the realm of chemical synthesis, it serves as a medium for conducting reactions that are sensitive to the presence of water, as it can help control the reaction environment. Additionally, its unique chemical structure, combining ether and ester functionalities, offers a useful model for studying reaction mechanisms and kinetics in synthetic organic chemistry, particularly in esterification and transesterification reactions. Its mild odor and good solvency power make it suitable for laboratory applications where less volatile and non-toxic conditions are preferred.


2-Methoxyethyl acetate (CAS 110-49-6) References

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  2. Comparative immunosuppression of various glycol ethers orally administered to Fischer 344 rats.  |  Smialowicz, RJ., et al. 1992. Fundam Appl Toxicol. 18: 621-7. PMID: 1526376
  3. The intensity of immunogold labeling of deplasticized acrylic sections compared to deplasticized epoxy sections-Theoretical deductions and experimental data.  |  Brorson, SH. and Reinholt, FP. 2008. Micron. 39: 144-50. PMID: 17188881
  4. Hydration structure of poly(2-methoxyethyl acrylate): comparison with a 2-methoxyethyl acetate model monomer.  |  Morita, S., et al. 2010. J Biomater Sci Polym Ed. 21: 1925-35. PMID: 20566058
  5. Detection of induced mitotic chromosome loss in Saccharomyces cerevisiae--an interlaboratory study.  |  Whittaker, SG., et al. 1989. Mutat Res. 224: 31-78. PMID: 2671714
  6. Continuous deacetylation of cephalosporins.  |  Konecny, J. and Sieber, M. 1980. Biotechnol Bioeng. 22: 2013-2029. PMID: 29345758
  7. Aneuploidy-inducing chemicals in yeast evaluated by the micronucleus test.  |  Basler, A. 1986. Mutat Res. 174: 11-3. PMID: 3517637
  8. Aprotic polar solvents inducing chromosomal malsegregation in yeast interfere with the assembly of porcine brain tubulin in vitro.  |  Gröschel-Stewart, U., et al. 1985. Mutat Res. 149: 333-8. PMID: 3887144
  9. Methoxyacetaldehyde, an intermediate metabolite of 2-methoxyethanol, is immunosuppressive in the rat.  |  Smialowicz, RJ., et al. 1993. Fundam Appl Toxicol. 21: 1-7. PMID: 8365577
  10. Solubilities of carbon dioxide in 2-methoxyethyl acetate, 1-methoxy-2-propyl acetate and 3-methoxybutyl acetate  |  Li, Yun, et al. 2014. The Journal of Chemical Thermodynamics. 74: 126-132.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Methoxyethyl acetate, 1 L

sc-238121
1 L
$135.00