Tridecanal (CAS 10486-19-8)
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Tridecanal is an organic compound classified as an aldehyde, specifically a long-chain aliphatic aldehyde with the chemical formula C13H26O. The presence of the aldehyde group makes it highly reactive, enabling it to undergo a range of chemical reactions typical of aldehydes. These reactions include but are not limited to oxidation, reduction, and condensation, making tridecanal a versatile compound in organic synthesis. Tridecanal finds applications in the field of organic chemistry for synthesis and research, serving as a precursor or intermediate in the production of more complex organic molecules. Its reactivity with various chemical agents can lead to the synthesis of alcohols, acids, esters, and other derivatives, expanding its utility in the creation of a wide array of chemical compounds. Additionally, due to its unique olfactory properties, tridecanal may be used in the flavor and fragrance industries, where it contributes to the aroma profiles of various products.
Tridecanal (CAS 10486-19-8) References
- Characterization of the odor-active volatiles in citrus Hyuganatsu (Citrus tamurana Hort. ex Tanaka). | Choi, HS., et al. 2001. J Agric Food Chem. 49: 2404-8. PMID: 11368611
- Chemical composition and antibacterial, antifungal and antioxidant activities of the flower oil of Retama raetam (Forssk.) Webb from Tunisia. | Edziri, H., et al. 2010. Nat Prod Res. 24: 789-96. PMID: 20461625
- Teratogenic effects of diatom metabolites on sea urchin Paracentrotus lividus embryos. | Romano, G., et al. 2010. Mar Drugs. 8: 950-67. PMID: 20479962
- Potentially important nighttime heterogeneous chemistry: NO3 with aldehydes and N2O5 with alcohols. | Iannone, R., et al. 2011. Phys Chem Chem Phys. 13: 10214-23. PMID: 21509392
- Bioluminescence decay kinetics in the reaction of bacterial luciferase with different aldehydes. | Ismailov, AD., et al. 1990. J Biolumin Chemilumin. 5: 213-7. PMID: 2220421
- RP-HPLC-fluorescence analysis of aliphatic aldehydes: application to aldehyde-generating enzymes HACL1 and SGPL1. | Mezzar, S., et al. 2014. J Lipid Res. 55: 573-82. PMID: 24323699
- Silencing of odorant binding protein gene AlinOBP4 by RNAi induces declining electrophysiological responses of Adelphocoris lineolatus to six semiochemicals. | Zhang, XY., et al. 2017. Insect Sci. 24: 789-797. PMID: 27265520
- A Search for CD36 Ligands from Flavor Volatiles in Foods with an Aldehyde Moiety: Identification of Saturated Aliphatic Aldehydes with 9-16 Carbon Atoms as Potential Ligands of the Receptor. | Tsuzuki, S., et al. 2017. J Agric Food Chem. 65: 6647-6655. PMID: 28682068
- Chemical composition of essential oil from plants of abandoned mining site of Elba island. | Pistelli, L., et al. 2019. Nat Prod Res. 33: 143-147. PMID: 29417841
- A comparative study on the essential oil composition and antibacterial activities of different organs of wild growing Paeonia daurica subsp. tomentosa from Iran. | Mahdavi Fikejvar, E., et al. 2019. Nat Prod Res. 33: 3153-3156. PMID: 30445858
- The quantitative impact of fluid vs. solid interfaces on the catalytic performance of pickering emulsions. | Stock, S., et al. 2021. Phys Chem Chem Phys. 23: 2355-2367. PMID: 33449989
- Bioprospecting of Less-Polar Constituents from Endemic Brown Macroalga Fucus virsoides J. Agardh from the Adriatic Sea and Targeted Antioxidant Effects In Vitro and In Vivo (Zebrafish Model). | Jerković, I., et al. 2021. Mar Drugs. 19: PMID: 33922234
- Essential oils composition of Litsea glauca and Litsea fulva and their anticholinesterase inhibitory activity. | Salleh, WMNHW., et al. 2023. Nat Prod Res. 1-5. PMID: 36794425
- Inhibition of thyroid NADPH-oxidase by 2-iodohexadecanal in a cell-free system. | Ohayon, R., et al. 1994. Mol Cell Endocrinol. 99: 133-41. PMID: 8187956
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Tridecanal, 1 g | sc-224321 | 1 g | $44.00 | |||
Tridecanal, 5 g | sc-224321A | 5 g | $98.00 |