Citropten
(Redirected from Limettin)
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| Names | |
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| Preferred IUPAC name
5,7-Dimethoxy-2H-1-benzopyran-2-one | |
| Other names
5,7-Dimethoxy-2H-chromen-2-one
5,7-Dimethoxycoumarin Citroptene Citraptene Limettin Limetin | |
| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.006.952 |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C11H10O4 | |
| Molar mass | 206.197 g·mol−1 |
| Melting point | 146 to 149 °C (295 to 300 °F; 419 to 422 K)[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Citropten is a natural organic compound with the molecular formula C11H10O4.[2] It is found in the essential oils of citrus such as lime, lemon, and bergamot.[3][4][5][6]
Properties
[edit]Studies suggest it possesses several potential properties:
- Antimicrobial activity – Citropten may exhibit antibacterial and antifungal properties.[7][better source needed] This characteristic could be relevant for applications in disinfectants or preservatives.
- Anti-inflammatory and antioxidant effects – Emerging research indicates citropten might have anti-inflammatory and antioxidant capabilities.[8] These properties could hold promise for various health applications.
The pleasant aroma of citropten makes it a valuable component in the fragrance industry, used in perfumes and cosmetics.[9] Its potential antimicrobial properties are also prompting exploration for use in medicine and pharmaceuticals.
References
[edit]- ^ "5,7-Dimethoxycoumarin". Sigma-Aldrich.
- ^ Chouchi, D.; Barth, D. (1994-06-24). "Rapid identification of some coumarin derivatives in deterpenated citrus peel oil by gas chromatography". Journal of Chromatography A. 672 (1–2): 177–183. doi:10.1016/0021-9673(94)80606-3. ISSN 0021-9673. PMID 8069393.
- ^ "Citropten". Merriam-Webster.
- ^ Makki, S.; Treffel, P.; Humbert, P.; Agache, P. (1991). "High-performance liquid chromatographic determination of citropten and bergapten in suction blister fluid after solar product application in humans". Journal of Chromatography B. 563 (2): 407–13. doi:10.1016/0378-4347(91)80049-I. PMID 2056004.
- ^ "5 Citrus Bergamot Benefits". Institute of botany. April 1, 2014. Retrieved 2024-04-04.
- ^ "5,7-Dimethoxycoumarin". pubchem.ncbi.nlm.nih.gov. Retrieved 2024-04-04.
- ^ "Buy Citropten | 487-06-9". Smolecule. Retrieved 2024-04-04.
- ^ "Effects of citropten bergamottin and bergapten on IL-8 mRNA accumulation". researchgate.net. Retrieved 2024-04-04.
- ^ Bettero, A.; Benassi, C.A. (1983-01-01). "Determination of bergapten and citropten in perfumes and suntan cosmetics by high-performance liquid chromatography and fluorescence". Journal of Chromatography A. 280: 167–171. doi:10.1016/s0021-9673(00)91554-1. ISSN 0021-9673.