24207
Nukol Capillary GC Column
size × I.D. 30 m × 0.32 mm, df 1.00 μm
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Recommended Products
material
fused silica
Agency
meets requirements for USP G25 and G35
parameter
60-200 °C temperature (isothermal)
60-220 °C temperature (programmed)
Beta value
80
df
1.00 μm
technique(s)
gas chromatography (GC): suitable
size × I.D.
30 m × 0.32 mm
matrix active group
Bonded; acid-modified poly(ethylene glycol) phase
application(s)
agriculture
chemicals and industrial polymers
cleaning products
clinical
cosmetics
food and beverages
forensics and toxicology
personal care
column type
capillary polar
Looking for similar products? Visit Product Comparison Guide
General description
Application: The incorporation of acid functional groups into the phase lends an acidic character to this column, useful for analyses of volatile acidic compounds. Difficult to analyze carboxylic acids (free fatty acids) can be analyzed with excellent peak shape and minimal adsorption.
USP Code: This column meets USP G25 and G35 requirements.
Phase:
USP Code: This column meets USP G25 and G35 requirements.
Phase:
- Bonded
- Acid-modified poly(ethylene glycol)
- 60 °C to 200 °C (isothermal) or 220 °C (programmed)
Application
Nukol Capillary GC Column may be used in the quantitative determination of C2-C8 free carboxylic acids in dairy products by gas chromatography. It may also be used for the determination of the free concentration of valproic acid in human plasma by equilibrium dialysis followed by solid-phase microextraction (SPME) and capillary gas chromatography.
Other Notes
We offer a variety of chromatography accessories including analytical syringes
Legal Information
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Journal of chromatography. B, Biomedical applications, 673(2), 299-305 (1995-11-17)
The potential of solid-phase microextraction in the bioanalysis of drugs is demonstrated. The free concentration of valproic acid in human plasma was determined by equilibrium dialysis at room temperature. To the dialysate was added an internal standard and the pH
Quantitative determination of free volatile fatty acids from dairy products on a Nukol capillary column.
Journal of Chromatography A, 519 (2), 369-378 (1990)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service