1653-31-2
1653-31-2
Chemical Structure
2-Tridecanol
- CAS No.: 1653-31-2
- Formula:C13H28O
- Molecular Weight:200.36
IUPAC Name: tridecan-2-ol
InChIKey: HKOLRKVMHVYNGG-UHFFFAOYSA-N
SMILES: CCCCCCCCCCCC(C)O
Biological Activity: 2-Tridecanol is a metabolite that can be found in extra virgin coconut oil, and serves as a growth substrate for Pseudomonas multivorans. 2-Tridecanol can be metabolized by Pseudomonas multivorans and Pseudomonas aeruginosa to produce 2-tridecanone, undecyl acetate, and 1-undecanol, and acts as a metabolic intermediate in their 2-tridecanone catabolic pathway[1][2][3][4][5].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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2-Tridecanol | 99.84% | 2-Tridecanol is a metabolite that can be found in extra virgin coconut oil, and serves as a growth substrate for Pseudomonas multivorans. 2-Tridecanol can be metabolized by Pseudomonas multivorans and Pseudomonas aeruginosa to produce 2-tridecanone, undecyl acetate, and 1-undecanol, and acts as a metabolic intermediate in their 2-tridecanone catabolic pathway. | ||||||||||||||||||||
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References
- [1]. Forney FW, et al. Oxidative degradation of methyl ketones. II. Chemical pathway for degradation of 2-tridecanone by Pseudomonas multivorans and Pseudomonas aeruginosa. J Bacteriol. 1968 Oct;96(4):1055-64. [Content Brief]
- [2]. Suzuki D, et al. Oiling-out effect improves the efficiency of extracting aroma compounds from edible oil. NPJ Sci Food. 2020 Nov 4;4(1):18. [Content Brief]
- [3]. Naccarato WF, et al. Characterization and metabolism of free fatty alcohols from Escherichia coli. Lipids. 1972 May;7(5):275-81. [Content Brief]
- [4]. Dimock MB, et al. Toxicity studies of analogs of 2-tridecanone, a naturally occurring toxicant from a wild tomato. J Chem Ecol. 1982 May;8(5):837-42. [Content Brief]
- [5]. Kramer, K. J., et al. Effects of 2-Tridecanone and Analogues on the Reproduction and Mortality of Stored Product Insects. Journal of the Kansas Entomological Society, 58(2), 254-260.
