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Caffeine ≥99% — chemical reagent for laboratory, research and analytical use. Not for human or animal consumption.
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WARNING: Chemical reagent intended solely for laboratory, research and analytical purposes. NOT FOR HUMAN OR ANIMAL CONSUMPTION. It is not a medicinal product, dietary supplement or food.
Olivetol is an organic compound of the alkylresorcinol group, formally 5-pentylbenzene-1,3-diol. Its molecule is a resorcinol ring (benzene-1,3-diol) bearing a straight-chain pentyl substituent at position 5. The presence of two adjacent phenolic hydroxyl groups together with an alkyl chain gives the compound both the reactivity characteristic of phenols and a degree of lipophilicity, making it a useful and versatile building block in organic synthesis.
The supplied material is purified olivetol of high declared purity, usually occurring as a viscous, pale oil or a low-melting solid ranging from colourless to pale yellow. Olivetol is a classic precursor and reference compound in resorcinol chemistry and in work on the synthesis of phenolic derivatives.
| Systematic name (IUPAC) | 5-pentylbenzene-1,3-diol |
| Synonyms | Olivetol, 5-pentylresorcinol, 5-amylresorcinol |
| CAS number | 500-66-3 |
| Molecular formula | C11H16O2 |
| Molar mass | 180.24 g/mol |
| Appearance | colourless or pale yellow solid / viscous oil |
| Solubility | soluble in ethanol, methanol and diethyl ether; poorly soluble in water |
| Melting point | no reliable data — omitted (material is often semi-solid) |
| Purity | ≥99% |
Olivetol is a valued building block in organic synthesis, primarily as a precursor in resorcinol chemistry. Its electron-rich aromatic ring readily undergoes electrophilic aromatic substitution, Friedel-Crafts alkylation and condensation reactions, which makes the compound a convenient substrate in multi-step synthetic sequences and in studies of alkylresorcinol chemistry.
In the laboratory, olivetol is used as an analytical standard and model compound in HPLC, GC-MS and NMR spectroscopy studies, where it serves for method validation and the identification of phenolic derivatives. It is also applied in natural product chemistry research and as a reference reagent in the development of procedures for determining alkylresorcinols in plant samples. Because of its phenolic groups, the material is sensitive to oxidation — it should be stored in a cool place, in a tightly closed container, protected from light and air, preferably under an inert gas atmosphere. All applications are strictly research in nature; the product is not intended for use on living organisms.