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• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Prenol lipids Acyclic monoterpenoids
• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Prenol lipids Monoterpenoids Acyclic monoterpenoids
• Solvents and Organic Chemicals Organic Compounds Acids/Esters
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons

Linalyl Propionate (CAS No. 144-39-8): An Overview of Its Properties, Applications, and Recent Research

Linalyl propionate (CAS No. 144-39-8) is a naturally occurring compound found in various essential oils, particularly those derived from lavender, coriander, and bergamot. This compound is a member of the ester family and is known for its pleasant, sweet, and floral aroma. In the realm of flavor and fragrance industries, linalyl propionate is highly valued for its ability to enhance the sensory experience of various products.

The chemical structure of linalyl propionate consists of a propionic acid ester linked to a linalyl group. The molecular formula is C12H20O2, with a molecular weight of approximately 196.28 g/mol. This structure contributes to its unique olfactory properties and its stability in different formulations. The compound is typically a colorless to pale yellow liquid at room temperature and is soluble in most organic solvents.

In recent years, there has been growing interest in the potential health benefits of linalyl propionate. Studies have explored its antimicrobial, anti-inflammatory, and antioxidant properties. For instance, a study published in the Journal of Agricultural and Food Chemistry in 2021 investigated the antimicrobial activity of linalyl propionate against various pathogenic bacteria. The results showed that it exhibited significant inhibitory effects on both Gram-positive and Gram-negative bacteria, making it a promising candidate for natural preservatives in food and cosmetic products.

Beyond its antimicrobial properties, linalyl propionate has also been studied for its potential anti-inflammatory effects. A 2020 study in the Inflammation Research journal demonstrated that this compound can reduce inflammation by inhibiting the production of pro-inflammatory cytokines such as TNF-α and IL-6. These findings suggest that linalyl propionate could be beneficial in the development of topical treatments for skin conditions characterized by inflammation.

The antioxidant properties of linalyl propionate have also been a subject of interest. Research published in the Oxidative Medicine and Cellular Longevity in 2019 found that it possesses strong free radical scavenging activity, which can help protect cells from oxidative damage. This property makes it a valuable ingredient in skincare products designed to combat aging and environmental stressors.

In addition to its applications in the flavor and fragrance industries, linalyl propionate has found use in aromatherapy. Its calming and relaxing effects have been documented in several studies, making it a popular choice for essential oil blends used to promote relaxation and reduce stress. A 2018 study in the Evidence-Based Complementary and Alternative Medicine journal reported that inhalation of lavender essential oil, which contains significant amounts of linalyl propionate, significantly reduced anxiety levels in participants.

The safety profile of linalyl propionate has been extensively evaluated. It is generally recognized as safe (GRAS) by regulatory bodies such as the Food and Drug Administration (FDA) when used within recommended concentrations. However, as with any chemical compound, proper handling and storage are essential to ensure its stability and efficacy.

In conclusion,

• 8007-75-8(BERGAMOT OIL)
• 2306-78-7(1,6,10-Dodecatrien-3-ol,3,7,11-trimethyl-, 3-acetate)
• 115-95-7(Linalyl acetate)
• 78-36-4(Butanoic acid,1-ethenyl-1,5-dimethyl-4-hexen-1-yl ester)
• 78-35-3(Linalyl isobutyrate)
• 1118-27-0(Butanoic acid,3-methyl-, 1-ethenyl-1,5-dimethyl-4-hexen-1-yl ester)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)