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grade
analytical standard
packaging
ampule of 100 mg
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
environmental
format
neat
storage temp.
room temp
SMILES string
Fc1ccc2ccccc2c1
InChI
1S/C10H7F/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H
InChI key
BAGQBTMEEISJLK-UHFFFAOYSA-N
General description
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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
149.0 °F - closed cup
Flash Point(C)
65 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
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)
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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