≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping
Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof
Cited in 72 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Vue d’ensemble
Application
1-Hexadecanol can be used as a reactant in the synthesis of self-assembled m -diethynylbenzene macrocycles (DBMs), water-soluble pillar[6]arene for controllable drug release and poly(ethylene glycol)-based polymer for intracellular delivery of anticancer drugs. It is used in building the template for sol-gel synthesis of mesoporous silicates. It can be employed in the synthesis of anionic gemini surfactants which also exhibit antibacterial and antifungal activities. High-chain fatty acid esters of 1-hexadecanol can be used as phase change materials (PCM) for thermal energy storage.
This compound belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms.
External Descriptors
a small molecule
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
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