442349
2-Fluoronaphthalene
analytical standard
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About This Item
Produits recommandés
Qualité
analytical standard
Conditionnement
ampule of 100 mg
Technique(s)
HPLC: suitable
gas chromatography (GC): suitable
Application(s)
environmental
Format
neat
Température de stockage
room temp
Chaîne SMILES
Fc1ccc2ccccc2c1
InChI
1S/C10H7F/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H
Clé InChI
BAGQBTMEEISJLK-UHFFFAOYSA-N
Description générale
2-Fluoronaphthalenes are mono-substituted naphthalenes, which belong to the class of polycyclic aromatic hydrocarbons (PAHs).
Application
2-Fluoronaphthalene has been used as a reference standard for the determination of the analyte in duloxetine hydrochloride active pharmaceutical ingredient (API) by reversed-phase high-performance liquid chromatography (RP-HPLC). It has also been used as an internal standard for the determination of fluoride in biological samples by gas chromatography-mass spectrometry (GC-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Mention d'avertissement
Danger
Mentions de danger
Conseils de prudence
Classification des risques
Acute Tox. 4 Oral - Eye Dam. 1
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
149.0 °F - closed cup
Point d'éclair (°C)
65 °C - closed cup
Équipement de protection individuelle
dust mask type N95 (US), Eyeshields, Gloves
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Sensitive determination of fluoride in biological samples by gas chromatography-mass spectrometry after derivatization with 2-(bromomethyl) naphthalene
Analytica Chimica Acta, 852(8), 162-167 (2014)
A Validated RP-HPLC Method for the Analysis of 1-fluoronaphthalene and its Process-Related Impurities
Journal of Chromatographic Science, 53(8), 1296-1302 (2015)
Resonant two-photon mass-analyzed threshold ionization spectroscopy of 1-fluoronaphthalene and 2-fluoronaphthalene
Journal of Molecular Spectroscopy, 281, 40-46 (2012)
Simple determination of fluoride in biological samples by headspace solid-phase microextraction and gas chromatography-tandem mass spectrometry
Journal of Chromatography A, 1407(8), 216-221 (2015)
European journal of medicinal chemistry, 44(5), 1941-1951 (2008-12-27)
A series of naphthalene and non-naphthalene derivatives (n=42) having cytochrome P450 2A6 and 2A5 inhibitory activities, reported by Rahnasto et al., were subjected to QSAR and QAAR studies. The analyses were performed using electronic, spatial, shape and thermodynamic descriptors to
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