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Methyl propionate (CAS 554-12-1)

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Alternate Names:
Propanoic acid, methyl ester; formyl propionate
Application:
Methyl propionate is a volatile odorant
CAS Number:
554-12-1
Molecular Weight:
88.11
Molecular Formula:
C4H8O2
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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Methyl propionate is an ester formed from methanol and propanoic acid. This organic compound is characterized by its sweet, fruity odor and is commonly used as a flavoring agent and solvent. Structurally, methyl propionate consists of a methyl group attached to the ester linkage of propanoic acid, contributing to its moderate volatility and solubility in organic solvents. In research contexts, methyl propionate serves as an important solvent in the synthesis of various chemical products due to its ability to dissolve a wide range of chemical substances, which is crucial for facilitating reactions and processes in organic synthesis. Its mechanism of action as a solvent is largely based on its polarity, which allows it to interact effectively with both polar and non-polar molecules, enhancing reaction kinetics and solute stability. Additionally, methyl propionate is used in the study of esterification reactions, where its formation and breakdown provide insights into reaction mechanisms and kinetics. The ester is also utilized in the field of polymer chemistry, particularly in the production of polyesters and as a carrier for polymer additives. In environmental research, methyl propionate is studied for its role in atmospheric chemistry, including its reactivity and breakdown products, which contribute to understanding photochemical smog formation and degradation pathways in the atmosphere.


Methyl propionate (CAS 554-12-1) References

  1. Atmospheric chemistry of two biodiesel model compounds: methyl propionate and ethyl acetate.  |  Andersen, VF., et al. 2011. J Phys Chem A. 115: 8906-19. PMID: 21797203
  2. Redirecting catalysis from proteolysis to perhydrolysis in subtilisin Carlsberg.  |  Despotovic, D., et al. 2013. J Biotechnol. 167: 279-86. PMID: 23835157
  3. Applicability of non-halogenated methyl propionate to microencapsulation.  |  Kang, J., et al. 2014. J Microencapsul. 31: 323-32. PMID: 24175715
  4. Methyl propionate radical cation.  |  Pakarinen, JM., et al. 1996. J Am Soc Mass Spectrom. 7: 482-9. PMID: 24203403
  5. Identification and Quantitation of Volatile Organic Compounds in Poly(methyl methacrylate) Kitchen Utensils by Headspace Gas Chromatography/Mass Spectrometry.  |  Ohno, H., et al. 2014. J AOAC Int. 97: 1452-8. PMID: 25902999
  6. Perspectives for the microbial production of methyl propionate integrated with product recovery.  |  Pereira, JPC., et al. 2018. Bioresour Technol. 256: 187-194. PMID: 29438919
  7. Cl-initiated photo-oxidation reactions of methyl propionate in atmospheric condition.  |  Balan, RC. and Balla, R. 2018. Environ Sci Pollut Res Int. 25: 20999-21010. PMID: 29766432
  8. RIFM fragrance ingredient safety assessment, methyl propionate, CAS Registry Number 554-12-1.  |  Api, AM., et al. 2022. Food Chem Toxicol. 167 Suppl 1: 113345. PMID: 35952823
  9. Infrared intensities of methyl acetate, an interstellar compound - comparisons of three organic esters.  |  Yarnall, YY. and Hudson, RL. 2022. Spectrochim Acta A Mol Biomol Spectrosc. 283: 121738. PMID: 35985234
  10. Weak-Coordination Electrolyte Enabling Fast Li+ Transport in Lithium Metal Batteries at Ultra-Low Temperature.  |  Lin, W., et al. 2023. Small. 19: e2207093. PMID: 36890773
  11. Fecal Microbiota and Associated Volatile Organic Compounds Distinguishing No-Adenoma from High-Risk Colon Adenoma Adults.  |  Katsaounou, K., et al. 2023. Metabolites. 13: PMID: 37512526

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Methyl propionate, 100 ml

sc-215367
100 ml
$51.00

Methyl propionate, 500 ml

sc-215367A
500 ml
$140.00