Name | Fluorene Myristate |
CAS number | 2595050-21-6 |
Description | This compound is a synthetic organic molecule formed by the esterification of a fluorene-based alcohol with myristic acid, resulting in a highly lipophilic ester. |
Structural formula |  |
Molecular Formula | C27H36O2 |
Molecular Weight | 392.57 g/mol |
Appearance | White powder |
Quality Standard | 99% |
Storage Condition | Cool dry place( away from the light) |
Shelf Life | >2 years if stored properly |
Sample package | Aluminium foil bag |
Commercial package | Aluminium Tin, Fiber drum |
Origin | China |
Fluorene Myristate More Info
This compound is a synthetic organic molecule formed by the esterification of a fluorene-based alcohol with myristic acid, resulting in a highly lipophilic ester. The fluorene moiety provides a rigid, planar aromatic structure, while the myristate side chain, derived from the 14-carbon saturated fatty acid myristic acid, introduces significant hydrophobic character. This design, combining an aromatic core with a long aliphatic tail, is common in the development of specialty chemicals intended to alter surface properties and enhance compatibility with non-polar environments.
The functionality of this compound is primarily derived from its amphiphilic nature and its ability to integrate into lipid-based systems. The aromatic fluorene segment can participate in pi-pi stacking interactions, potentially contributing to self-assembly or ordered structures, while the long fatty acid chain promotes solubility in organic solvents and miscibility with oils, waxes, and polymers. This dual character makes it suitable for applications where modifying the interfacial properties between polar and non-polar phases is desired.
One potential application area for such a molecule is in advanced material science and polymer chemistry. It could be investigated as a monomer for creating novel polyesters or as a modifying agent to plasticize or alter the surface energy of polymeric materials. Additionally, its structure makes it a candidate for use in organic electronic research as part of a charge-transport layer or as a precursor for more complex semiconducting molecules, where the fluorene unit is a common building block.
From a chemical handling and development perspective, a compound of this type would typically be a solid at room temperature, with its melting point determined by the balance between the rigid fluorene group and the flexible alkyl chain. Its synthesis involves standard esterification protocols under controlled conditions. As a research chemical, it would be of interest for studying structure-property relationships, particularly in the development of new surfactants, lubricant additives, or photoresist materials in microfabrication.
The safety profile of this specific compound is not widely documented in public literature, as it appears to be a relatively new or niche research chemical. General precautions for handling fine organic powders and potential irritants should be observed. The environmental fate of such a lipophilic, persistent aromatic ester would require evaluation regarding biodegradation and bioaccumulation potential. Its utility lies predominantly in its role as a specialized synthetic intermediate or functional additive in controlled industrial or laboratory research contexts, rather than in consumer-facing applications.
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