Astec® CHIRALDEX® and Supelco® DEX™ - Chiral GC Columns
Brochures and specifications | 2013 | MerckInstrumentation
The ability to separate enantiomers by gas chromatography is vital in pharmaceutical, flavor, fragrance and environmental analysis. Cyclodextrin‐based chiral stationary phases (CSPs) enable selective interaction with mirror‐image isomers, ensuring accurate quantification, purity assessment and compliance with regulatory requirements.
This work surveys two families of derivatized cyclodextrin GC columns, Astec CHIRALDEX and Supelco DEX, covering 24 distinct chemistries. It outlines the structural basis of enantioselection, compares surface, inclusion and mixed interaction mechanisms, and delivers practical guidelines for phase selection and method development.
Chiral GC separations employ columns coated or doped with derivatized α, β or γ cyclodextrins. Key factors include cyclodextrin cavity size, degree and position of substitution, type of derivative and polymer carrier. Typical analyses use helium carrier gas, split or splitless injection, flame ionization detection and temperature programming up to 230 °C. Screening kits combine complementary phases for rapid identification of optimal selectivity.
Cyclodextrin derivatives fall into three groups: complex surface‐interaction phases (γ‐based), combined surface and inclusion phases (β‐based) and strict inclusion phases (all three sizes). Unique complex derivatives in the Astec line offer stronger surface selectivity. A six‐column screening set is recommended to cover common analyte classes such as alcohols, amines, acids, terpenes and multiring structures. Column selection charts link analyte types to CSP chemistry.
These CSPs deliver high enantioselectivity, robust performance, low bleed and long lifetimes. They address applications from chiral drug intermediates and metabolites to essential oil profiling, amino acid analysis and environmental monitoring.
Advances may include novel cyclodextrin derivatives, integration with GC–MS, tailored CSPs for high‐throughput screening, and scaling chiral separations to preparative or simulated moving bed processes for active pharmaceutical ingredient production.
Cyclodextrin‐based CSPs provide a versatile toolkit for enantiomeric separations in GC. Systematic phase selection and screening strategies accelerate method development, ensuring reproducible, high‐resolution analyses across diverse chemical classes.
Gas chromatograph equipped with split/splitless inlet, capillary columns (30 m×0.25 mm I.D., film thickness 0.12–0.25 µm), flame ionization detector, helium carrier gas, optional SPME sampling for volatiles.
1. Armstrong DW and DeMond W. J Chromatogr Sci 1984;22:411–415.
2. Armstrong DW, Tang Y, Zukowski Y. Anal Chem 1991;63(24):2858–2861.
3. Armstrong DW and Jin HL. J Chromatogr 1990;502:154–159.
4. Armstrong DW, Li W, Pitha J. Anal Chem 1990;62:214–217.
5. Li W, Jin HL, Armstrong DW. J Chromatogr 1990;509:303–324.
6. Harada K. Chem Rev 1998;98:1803–1827.
GC, SPME, GC columns, Consumables
IndustriesManufacturerMerck
Summary
Importance of the Topic
The ability to separate enantiomers by gas chromatography is vital in pharmaceutical, flavor, fragrance and environmental analysis. Cyclodextrin‐based chiral stationary phases (CSPs) enable selective interaction with mirror‐image isomers, ensuring accurate quantification, purity assessment and compliance with regulatory requirements.
Objectives and Overview
This work surveys two families of derivatized cyclodextrin GC columns, Astec CHIRALDEX and Supelco DEX, covering 24 distinct chemistries. It outlines the structural basis of enantioselection, compares surface, inclusion and mixed interaction mechanisms, and delivers practical guidelines for phase selection and method development.
Methodology and Instrumentation
Chiral GC separations employ columns coated or doped with derivatized α, β or γ cyclodextrins. Key factors include cyclodextrin cavity size, degree and position of substitution, type of derivative and polymer carrier. Typical analyses use helium carrier gas, split or splitless injection, flame ionization detection and temperature programming up to 230 °C. Screening kits combine complementary phases for rapid identification of optimal selectivity.
Main Results and Discussion
Cyclodextrin derivatives fall into three groups: complex surface‐interaction phases (γ‐based), combined surface and inclusion phases (β‐based) and strict inclusion phases (all three sizes). Unique complex derivatives in the Astec line offer stronger surface selectivity. A six‐column screening set is recommended to cover common analyte classes such as alcohols, amines, acids, terpenes and multiring structures. Column selection charts link analyte types to CSP chemistry.
Benefits and Practical Applications
These CSPs deliver high enantioselectivity, robust performance, low bleed and long lifetimes. They address applications from chiral drug intermediates and metabolites to essential oil profiling, amino acid analysis and environmental monitoring.
Future Trends and Potential Applications
Advances may include novel cyclodextrin derivatives, integration with GC–MS, tailored CSPs for high‐throughput screening, and scaling chiral separations to preparative or simulated moving bed processes for active pharmaceutical ingredient production.
Conclusion
Cyclodextrin‐based CSPs provide a versatile toolkit for enantiomeric separations in GC. Systematic phase selection and screening strategies accelerate method development, ensuring reproducible, high‐resolution analyses across diverse chemical classes.
Instrumentation
Gas chromatograph equipped with split/splitless inlet, capillary columns (30 m×0.25 mm I.D., film thickness 0.12–0.25 µm), flame ionization detector, helium carrier gas, optional SPME sampling for volatiles.
Reference
1. Armstrong DW and DeMond W. J Chromatogr Sci 1984;22:411–415.
2. Armstrong DW, Tang Y, Zukowski Y. Anal Chem 1991;63(24):2858–2861.
3. Armstrong DW and Jin HL. J Chromatogr 1990;502:154–159.
4. Armstrong DW, Li W, Pitha J. Anal Chem 1990;62:214–217.
5. Li W, Jin HL, Armstrong DW. J Chromatogr 1990;509:303–324.
6. Harada K. Chem Rev 1998;98:1803–1827.
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