Z226238
Nucleosil® C8 HPLC Column
5 μm particle size, L × I.D. 25 cm × 4.6 mm
Sinónimos:
Octyl Silica Column
About This Item
Productos recomendados
agency
suitable for USP L7
product line
Nucleosil®
feature
endcapped: no
manufacturer/tradename
Nucleosil®
extent of labeling
8.5% Carbon loading
parameter
400 bar pressure (5801 psi)
technique(s)
HPLC: suitable
L × I.D.
25 cm × 4.6 mm
surface area
350 m2/g
matrix
octyl
matrix active group
C8 (octyl) phase
particle size
5 μm
pore size
100 Å
separation technique
reversed phase
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Application
- Determination of melamine in milk and dairy products by high performance liquid chromatography.: This study describes the use of the Nucleosil® C8 HPLC column for determining melamine contamination in dairy products, highlighting its efficiency in food safety applications (Filazi et al., 2012).
- Validation of a novel, fully automated high throughput high-performance liquid chromatographic/tandem mass Spectrometric method for quantification of pantoprazole in human plasma.: Utilizes Nucleosil® C8 HPLC column to establish a rapid and reliable method for plasma analysis in clinical pharmacokinetic studies (Dotsikas et al., 2010).
- Simultaneous determination of alprazolam and fluoxetine hydrochloride in tablet formulations by high-performance column liquid chromatography and high-performance thin-layer chromatography.: Demonstrates the versatility of Nucleosil® C8 columns in pharmaceutical analysis, ensuring precise quantification in complex matrices (Patel et al., 2009).
- Simultaneous estimation of acetylsalicylic acid and clopidogrel bisulfate in pure powder and tablet formulations by high-performance column liquid chromatography and high-performance thin-layer chromatography.: Features the application of Nucleosil® C8 in dual-drug analysis, proving its capability in simultaneous analytical tasks (Patel et al., 2008).
- Validated HPLC method for determination of amlodipine in human plasma and its application to pharmacokinetic studies.: This research highlights the column′s role in the pharmacokinetic evaluation of cardiovascular drugs, underscoring its reliability and reproducibility (Zarghi et al., 2005).
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