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HCID 7129Erstellt: 4. November 2026

Ethyl-2-naphthylether

NEROLIN BROMELIA · NEROLIN · NEROLINE · NEROLINE BROMELIA · Naphthalene, 2-ethoxy- · BROMELIA · FEMA 2768 · ETHYL 2-NAPHTHYL ETHER

https://huagongshe.com/de/chemical/7129

Molekülstruktur von Ethyl-2-naphthylether

Identifikatoren & physikalische Daten

CAS No.93-18-5
SummenformelC12H12O
Durchschnittliche Molmasse172,22 g/mol
Monoisotopische Masse172,088815 g/mol
SMILESCCOc1ccc2ccccc2c1
InChIKeyGUMOJENFFHZAFP-UHFFFAOYSA-N
PubChem CID7129
ChEBICHEBI:173790
EC No.202-226-7
DTXSIDDTXSID2049684
Lokaler NameEthyl-2-naphthylether

Chemische & physikalische Eigenschaften

XLogP3,8
Polarare Oberfläche (TPSA)9,2
H-Brücken-Donoren0
H-Brücken-Akzeptoren1
Frei drehbare Bindungen2
Schwere Atome13
Formalladung0
Komplexität155
SpringerMaterials PropertiesAngular frequency
DuftstoffeFragrance Ingredient (beta-Naphthyl ethyl ether) -> IFRA transparency List
LebensmittelzusatzstoffeFLAVOR ENHANCER, FLAVORING AGENT OR ADJUVANT -> FDA Substance added to food
AromastoffeEU Flavoring substances
LöslichkeitInsoluble in water, soluble in oilssoluble (in ethanol)alcohol: soluble
Siedepunkt282.00 °C. @ 760.00 mm Hg282°C
Schmelzpunkt37.5 °C35-37 °C(lit.)
Physical DescriptionLiquidSolidWhite crystalline material, aroma suggestive of orange blossom
Dichte1.0640
Dampfdruck0.518Pa at 25℃
Brechungsindex1.5975 (estimate)
FEMA2768 | BETA-NAPHTHYL ETHYL ETHER
Flammpunkt134°C
LagerbedingungenStore at room temperature
FarbeWhite to Almost white
Geruchat 10.00 % in dipropylene glycol. naphtha floral orange blossom powdery grape
Geruchsartnaphthyl
Biologische Quellesynthetic
Merck14,3752
JECFA Number1258
BRN2042397
Hauptanwendungenflavors and fragrances
Kosmetik-Inhaltsstoffe FunktionenPERFUMING
InChI1S/C12H12O/c1-2-13-12-8-7-10-5-3-4-6-11(10)9-12/h3-9H,2H2,1H3
InChIKeyGUMOJENFFHZAFP-UHFFFAOYSA-N
SMILESCCOc1ccc2ccccc2c1
LogP (Verteilungskoeffizient)3.747 at 25℃
CAS Datenbank93-18-5(CAS DataBase Reference)
NIST chemische InformationenNaphthalene, 2-ethoxy-(93-18-5)
EPA chemische InformationenNaphthalene, 2-ethoxy- (93-18-5)

Sicherheit & Vorschriften

GHS-EinstufungThis chemical does not meet GHS hazard criteria for 2% (38 of 1877) of reports.WarningH315 (95.5%): Causes skin irritation [Warning Skin corrosion/irritation]P264, P264+P265, P273, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, P362+P364, P391, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 1877 reports by companies from 11 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Regulatorische InformationenChemical: Naphthalene, 2-ethoxy-Commission Regulation (EC) No 1565/2000 (Repealed by Com. Implementing Reg. (EU) No 872/2012)Naphthalene, 2-ethoxy- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Naphthalene, 2-ethoxy- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)REACH registered substance: Ethyl 2-naphthyl ether (EC: 202-226-7)2-Ethoxynaphthalene: Does not have an individual approval but may be used under an appropriate group standard
Hazard Classes and CategoriesSkin Irrit. 2 (95.5%)
Wassergefährdungsklasse (WGK)2
TSCA-Inventar-StatusTSCA listed
Zollcode29093090
RTECS-Nr.QJ6900000
R-Sätze (R)38
GefahrensymboleXi
Sicherheitshinweise (S)26-36-24/25
Lagerklasse11 - Combustible Solids
GefahrenklasseSkin Irrit. 2

Anwendungen & Verwendung

Beschreibung

Das 2-Ethoxynaphthalin bildet farblose, wasserunlösliche, nach Akazienblüten riechende Kristalle. Es wurde früher häufig in der Parfümindustrie verwendet, ist heute aber ohne große Bedeutung.

Beschreibung

(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.

Verwenden

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 .

Herstellung & Synthese

synthetische

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.