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Merck
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重要文件

442349

Supelco

2-氟萘

analytical standard

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About This Item

CAS號碼:
EC號碼:
MDL號碼:
分類程式碼代碼:
12000000
PubChem物質ID:

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.

象形圖

CorrosionExclamation mark

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


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分析證明 (COA)

Lot/Batch Number

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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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