等級
analytical standard
包裝
ampule of 100 mg
技術
HPLC: suitable
gas chromatography (GC): suitable
應用
environmental
形式
neat
儲存溫度
room temp
SMILES 字串
Fc1ccc2ccccc2c1
InChI
1S/C10H7F/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H
InChI 密鑰
BAGQBTMEEISJLK-UHFFFAOYSA-N
一般說明
2-Fluoronaphthalenes are mono-substituted naphthalenes, which belong to the class of polycyclic aromatic hydrocarbons (PAHs).
應用
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.
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 4 Oral - Eye Dam. 1
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
149.0 °F - closed cup
閃點(°C)
65 °C - closed cup
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
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)
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)
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)
Laura E Korhonen et al.
Journal of medicinal chemistry, 48(11), 3808-3815 (2005-05-27)
The purpose of this study was to determine the cytochrome P450 1A2 (CYP1A2) inhibition potencies of structurally diverse compounds to create a comprehensive three-dimensional quantitative structure-activity relationship (3D-QSAR) model of CYP1A2 inhibitors and to use this model to predict the
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