Cas no 6293-37-4 (2-Ethylhexyl Propanoate)

2-Ethylhexyl Propanoate is an ester compound commonly used as a solvent or intermediate in industrial and specialty chemical applications. Its key advantages include a favorable balance of low volatility and moderate evaporation rate, making it suitable for formulations requiring controlled drying properties. The branched alkyl structure contributes to good solvency for resins, polymers, and oils while maintaining compatibility with many organic systems. It exhibits low water solubility and relatively high stability under typical processing conditions. The compound's mild odor and low acute toxicity profile enhance its utility in coatings, inks, and adhesive formulations where worker exposure may be a consideration. Its chemical properties can be tailored for specific performance requirements in end-use applications.
2-Ethylhexyl Propanoate structure
2-Ethylhexyl Propanoate structure
Product Name:2-Ethylhexyl Propanoate
CAS No:6293-37-4
MF:C11H22O2
MW:186.291183948517
CID:514009
PubChem ID:95425
Update Time:2025-06-08

2-Ethylhexyl Propanoate Chemical and Physical Properties

Names and Identifiers

    • Propanoic acid,2-ethylhexyl ester
    • 2-ETHYL HEXYL PROPIONATE
    • Propionat des 2-Ethylhexanols
    • 6293-37-4
    • 2-ethylhexyl propanoate
    • Propanoic acid, 2-ethylhexyl ester
    • 2-Ethyl-1-hexanol propionate; 2-Ethylhexyl Propionate; NSC 8902; Propionic Acid 2-Ethylhexyl Ester
    • NS00043884
    • CS-0098410
    • AKOS006278790
    • D75927
    • NSC-8902
    • EINECS 228-551-4
    • AI3-33699
    • NSC8902
    • NSC 8902
    • 2-Ethylhexyl propionate
    • SCHEMBL1155390
    • DTXSID60863739
    • 2-Ethylhexyl Propanoate
    • Inchi: 1S/C11H22O2/c1-4-7-8-10(5-2)9-13-11(12)6-3/h10H,4-9H2,1-3H3
    • InChI Key: GUHQWKGQAYBNEW-UHFFFAOYSA-N
    • SMILES: O(C(CC)=O)CC(CC)CCCC

Computed Properties

  • Exact Mass: 186.16200
  • Monoisotopic Mass: 186.161979940g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 8
  • Complexity: 132
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 3.7
  • Topological Polar Surface Area: 26.3?2

Experimental Properties

  • PSA: 26.30000
  • LogP: 3.15600

2-Ethylhexyl Propanoate Pricemore >>

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Additional information on 2-Ethylhexyl Propanoate

Professional Introduction to 2-Ethylhexyl Propanoate (CAS No. 6293-37-4)

2-Ethylhexyl Propanoate, also known by its Chemical Abstracts Service (CAS) number 6293-37-4, is an ester compound that has garnered significant attention in the field of chemical and pharmaceutical research. This compound, with its unique molecular structure, exhibits a range of properties that make it valuable in various industrial and scientific applications. The molecular formula of 2-Ethylhexyl Propanoate is C10H20O2, and it is commonly used as a solvent, fragrance component, and intermediate in the synthesis of more complex molecules.

The compound's versatility stems from its balanced solubility profile, which allows it to dissolve in both polar and non-polar solvents. This characteristic makes it an excellent choice for applications where compatibility with multiple solvent systems is required. In the pharmaceutical industry, 2-Ethylhexyl Propanoate is often utilized as a carrier for active pharmaceutical ingredients (APIs), enhancing their stability and bioavailability. Its low toxicity and mild odor profile further contribute to its widespread use in formulations intended for human consumption.

Recent advancements in the field of drug delivery systems have highlighted the potential of 2-Ethylhexyl Propanoate as a vehicle for controlled-release formulations. Research has demonstrated that this ester can be incorporated into polymeric matrices to create sustained-release mechanisms, improving the efficacy of therapeutic agents. For instance, studies have shown that when combined with hydrophilic polymers, 2-Ethylhexyl Propanoate can enhance the release profile of anti-inflammatory drugs, leading to prolonged therapeutic effects and reduced dosing frequency.

In addition to its pharmaceutical applications, 2-Ethylhexyl Propanoate plays a crucial role in the cosmetics industry. Its ability to function as a fixative in fragrance compositions allows for the creation of long-lasting perfumes and scents. The compound's low evaporation rate ensures that aromatic molecules remain active on the skin for extended periods, providing consumers with a more enjoyable and enduring olfactory experience. Furthermore, its compatibility with various cosmetic bases makes it a preferred choice for formulators seeking to develop high-quality skincare and haircare products.

The chemical synthesis of 2-Ethylhexyl Propanoate involves the esterification of propanoic acid with 2-ethylhexanol. This reaction is typically catalyzed by strong acids or enzymes, such as lipases, which facilitate the formation of the ester bond under mild conditions. The choice of catalyst can significantly influence the yield and purity of the product, making process optimization a critical aspect of industrial production. Recent innovations in biocatalysis have led to the development of more environmentally friendly synthetic routes, reducing reliance on harsh chemical reagents and minimizing waste generation.

The environmental impact of 2-Ethylhexyl Propanoate has also been a subject of extensive research. Studies have investigated its biodegradability and potential effects on aquatic ecosystems. Fortunately, preliminary findings suggest that this compound undergoes gradual degradation under natural conditions, posing minimal risk to environmental health. However, further research is necessary to fully understand its long-term ecological footprint. Regulatory agencies continue to monitor the use of such compounds closely to ensure compliance with safety standards and sustainable practices.

The economic significance of 2-Ethylhexyl Propanoate cannot be overstated. As demand for high-performance solvents and intermediates grows, this compound has become an essential component in numerous manufacturing processes. Its relatively low cost compared to other specialty esters makes it an attractive option for industries operating on tight budgets. Additionally, its adaptability across multiple sectors ensures a steady market demand, contributing to its sustained commercial success.

Looking ahead, the future prospects for 2-Ethylhexyl Propanoate appear promising. Ongoing research aims to expand its applications into emerging fields such as nanotechnology and advanced materials science. For example, scientists are exploring its potential use as a solvent in the synthesis of functionalized nanoparticles, which could revolutionize drug delivery and material engineering. As innovation continues to drive new uses for this versatile compound, its importance in both academic research and industrial applications is expected to grow even further.

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