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About This Item
CAS Number:
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:
Recommended Products
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).[1]
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).[2] It has also been used as an internal standard for the determination of fluoride in biological samples by gas chromatography-mass spectrometry (GC-MS).[3][4]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
149.0 °F - closed cup
flash_point_c
65 °C - closed cup
ppe
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
Karagiannidou E, et al.
Journal of Chromatographic Science, 53(8), 1296-1302 (2015)
Resonant two-photon mass-analyzed threshold ionization spectroscopy of 1-fluoronaphthalene and 2-fluoronaphthalene
Tzeng SY, et al.
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
Kwon SM and Shin HS
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
Kwon SM and Shin HS
Journal of Chromatography A, 1407(8), 216-221 (2015)
Kunal Roy et al.
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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