557-61-9
557-61-9
Chemical Structure
1-Octacosanol
- CAS No.: 557-61-9
- Formula:C28H58O
- Molecular Weight:410.77
IUPAC Name: octacosan-1-ol
InChIKey: CNNRPFQICPFDPO-UHFFFAOYSA-N
SMILES: CCCCCCCCCCCCCCCCCCCCCCCCCCCCO
Biological Activity: 1-Octacosanol is a straight-chain aliphatic 28-carbon fatty alcohol and a major component of the cholesterol-lowering agent Policosanol. 1-Octacosanol exhibits various activities such as anti-fatigue, anti-angiogenic, cholesterol-lowering, and insecticidal effects[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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1-Octacosanol | 98.0% | 1-Octacosanol is a straight-chain aliphatic 28-carbon fatty alcohol and a major component of the cholesterol-lowering agent Policosanol. 1-Octacosanol exhibits various activities such as anti-fatigue, anti-angiogenic, cholesterol-lowering, and insecticidal effects. | ||||||||||||||||||||
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Nonacosane | 98.0% | Nonacosane, isolated from Baphia massaiensis, exhibits weak activities against E. coli, B. subtilis, P. aeruginosa and S. aureus. | ||||||||||||||||||||
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1-Triacontanol | 98.0% | 1-Triacontanol is a naturally occurring plant growth regulator. 1-Triacontanol is a saturated long-chain alcohol that has growth-promoting activities on a number of plants. 1-Triacontanol has anticancer activity. | ||||||||||||||||||||
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1-Heptacosanol | 98.0% | 1-Heptacosanol (Heptacosan-1-ol) is a long-chain fatty alcohol with antifungal, antibacterial (against Escherichia coli and Staphylococcus aureus), nematicidal, anticancer and antioxidant activities. 1-Heptacosanol can be isolated from leaf extracts of Ficus septica and Lecaniodiscus cupanioides. 1-Heptacosanol not only effectively resists pathogenic fungal infections, but also shows potential against pepper anthracnose in phytopathology. 1-Heptacosanol can be used in the research of fungal infections, cancer and oxidative stress-related diseases. |
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1-Tricosanol | 98.0% | 1-Tricosanol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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Nonacosanoic Acid | Nonacosanoic Acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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Lignoceryl alcohol | 98.0% | Lignoceryl alcohol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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1-Hexacosanol | 98.0% | 1-Hexacosanol can be used as an inhibitor of acetylcholinesterase (AChE). 1-Hexacosanol has larvicidal activity and can inhibit the acetylcholinesterase activity of Culex quinquefasciatus, Aedes aegypti and Chironomus riparius, exerting neurotoxic effects. | ||||||||||||||||||||
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Triacontane | 99.15% | Triacontane is an ester product. | ||||||||||||||||||||
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Octacosane (Standard) | ≥98% | Octacosane (Standard) is the analytical standard of Octacosane. This product is intended for research and analytical applications. Octacosane is an endogenous metabolite with antibacterial activity. Octacosane shows high cytotoxicity against murine melanoma B16F10-Nex2 cells besides inducing protection against a grafted subcutaneous melanoma. Octacosane has the larvicidal activity against mosquito Culex quinquefasciatus with the LC50 concentration of 7.2 mg/l. | ||||||||||||||||||||
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Tetratriacontanol | Tetratriacontanol is an ester product. | |||||||||||||||||||||
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References
- [1]. Gao W, et al. High-performance thin-layer chromatography for quantification of 1-octacosanol in Antarctic krill (Euphausia superba Dana). J Chromatogr Sci. 2015 May-Jun;53(5):811-5. [Content Brief]
- [2]. Zavala-Sánchez M Á, et al. Bioactivity of 1-octacosanol from Senna crotalarioides (Fabaceae: Caesalpinioideae) to control Spodoptera frugiperda (Lepidoptera: Noctuidae). Florida Entomologist, 2020, 102(4): 731-737.
- [3]. Marrero Delange D, et al. Trace determination of 1-octacosanol in rat plasma by solid-phase extraction with Tenax GC and capillary gas chromatography. J Chromatogr B Biomed Sci Appl. 2001 Oct 5;762(1):43-9. [Content Brief]
