| Description | (β-Naphthyl ethyl ether has an odor suggestive of orange blossom with a faint, fruity undertone. It has a corresponding sweet taste suggestive of strawberry (on extreme dilution only). This substance may be prepared by esterification of P-naphthol with ethyl alcohol and sulfuric acid; from β-naphtholsodium and diethylsulfate in weak aqueous base; fromβ-naphtholsodium and ethyl bromide. |
| Chemical Properties | β-Naphthyl ethyl ether has an odor suggestive of orange blossom with a faint, fruity undertone. Also, it has a corresponding sweet taste suggestive of strawberry (on extreme dilution only) |
| Chemical Properties | Ethyl 2-Naphthyl Ether forms white crystals (mp 37–38°C), with a mild, long-lasting, orange blossom fragrance. |
| Chemical Properties | light brown crystals |
| Uses | The fluorescence of 2-Ethoxynaphthalene has been shown to be weakly quenched by m-dimethlphthalate and methyl benzoate. Importantly, at increased concentration methyl benzoate enhances the fluorescence by increasing the polarity of the solvent . |
| Preparation | By esterification of β-naphthol with ethyl alcohol and sulfuric acid; from β-naphtholsodium and diethylsulfate in weak
aqueous base; from β-naphtholsodium and ethyl bromide. |
| Definition | ChEBI: 2-Ethoxynaphthalene is a member of naphthalenes. |
| Taste threshold values | Taste characteristics at 4 ppm: powdery, floral, soapy and heavy with a berry and grape nuance. |
| General Description | Nerolin bromelia is an alkyl ether of 2-naphthol, which is generally used as a perfume and flavoring compound. |
| Flammability and Explosibility | Notclassified |
| Purification Methods | Crystallise it from pet ether or EtOH (m 37-38o). Dry it in vacuo, or distil it in a vacuum. The picrate has m 104.5o (from EtOH or CHCl3). [Beilstein 6 H 606, 6 II 578, 6 III 2972, 6 IV 4257.] |
