GCMS
More information
WebinarsAbout usContact usTerms of use
LabRulez s.r.o. All rights reserved. Content available under a CC BY-SA 4.0 Attribution-ShareAlike

β-citronellol - Rt-βDEXsa™

Applications |  | RestekInstrumentation
GC, GC columns, Consumables
Industries
Food & Agriculture
Manufacturer
Restek

Summary

Significance of Enantiomeric Analysis of β-Citronellol


Chiral alcohols such as β-citronellol play a critical role in fragrance, flavor and pharmaceutical industries. Their enantiomers often exhibit distinct organoleptic profiles and biological activities. Reliable separation and quantification of (R)- and (S)-β-citronellol is therefore essential for quality control, regulatory compliance and product optimization.

Objectives and Study Overview


This application note demonstrates a gas chromatographic method for baseline resolution of (–)-(S)-β-citronellol and (+)-(R)-β-citronellol using a Rt-βDEXsa™ chiral column. The goal is to establish a robust protocol that delivers reproducible retention times and sharp peak shapes for routine enantiomeric analysis.

Applied Instrumentation


  • Gas chromatograph equipped with flame ionization detector (FID)
  • Rt-βDEXsa™ chiral column, 30 m × 0.32 mm ID, 0.25 µm film (Restek cat. #13108)
  • Carrier gas: hydrogen, linear velocity 80 cm/s set at 40 °C
  • Oven temperature program: 40 °C hold 1 min, ramp to 230 °C at 2 °C/min, hold 3 min
  • Injector and detector temperature: 220 °C

Methodology


Samples of racemic β-citronellol are injected under split or splitless conditions appropriate for concentration range. The hydrogen carrier ensures efficient mass transfer and narrow peaks. The chosen temperature program provides adequate separation without excessive analysis time. Enantiomer identities are confirmed by retention order: S‐enantiomer elutes before R‐enantiomer.

Main Results and Discussion


The developed method achieves baseline separation of the two enantiomers with retention times of approximately 51 min for (–)-(S)-β-citronellol and 52 min for (+)-(R)-β-citronellol. Peak symmetry and resolution factors consistently exceed acceptance criteria for chiral analyses. Hydrogen as carrier gas reduces analysis time and peak broadening compared to helium.

Benefits and Practical Applications


  • High resolution ensures accurate enantiomeric purity determination.
  • Hydrogen carrier reduces run time and operational cost.
  • Method is adaptable for similar monoterpenoid alcohols.
  • Suitable for quality control in flavor, fragrance and pharmaceutical production.

Future Trends and Potential Applications


Advances in fast GC and multidimensional chromatography may shorten analysis times further. Combining chiral separations with mass spectrometric detection can improve sensitivity for trace-level enantiomeric impurities. Green analytical approaches, such as alternative carrier gases and reduced energy programs, will enhance sustainability. There is potential to apply this method to other chiral terpenes and expand to enantioselective metabolite profiling.

Conclusion


The outlined GC-FID method on a Rt-βDEXsa™ column provides a reliable, cost-effective approach for enantiomeric separation of β-citronellol. It meets industry requirements for resolution, repeatability and throughput, supporting rigorous quality assurance in multiple industrial sectors.

Content was automatically generated from an orignal PDF document using AI and may contain inaccuracies.

Downloadable PDF for viewing
 

Similar PDF

Toggle
Geranium Oil (Commercial) - Rt-βDEXsa™
Geranium Oil (Commercial) Rt-βDEXsa™ 1a. 1b. 2a. 2b. 3. 4. 5a. 5b. 6a. 6b. 7. 8. (+)-(2R,4S)-cis-rose oxide (-)-(2S,4R)-cis-rose oxide (-)-(2R,4R)-trans-rose oxide (+)-(2S,4S)-trans-rose oxide isomenthone menthone (-)-(R)-linalool (+)-(S)-linalool (-)-(S)-β-citronellol (+)-(R)-β-citronellol 3 geraniol citronellyl formate 6a 6b 8 7 5a 5b…
Key words
citronellol, citronellollinalool, linaloolβdexsa, βdexsageranium, geraniumisomenthone, isomenthonecitronellyl, citronellylmenthone, menthonegeraniol, geraniolformate, formatecommercial, commercialhydrogen, hydrogenoil
A Guide to the Analysis of Chiral Compounds by GC
Technical Guide A Guide to the Analysis of Chiral Compounds by GC Inside: Definitions of Chirality and Chiral Chromatography Chiral Columns Offer Unique Selectivity Optimization of Chiral Separations Chiral Specific Applications of Essential Oils, Flavors, and Pharmaceuticals 2 A team…
Key words
chiral, chirallinalool, linaloolβdexcst, βdexcstβdexsm, βdexsmlinalyl, linalylenantiomeric, enantiomericenantiomers, enantiomersβdexse, βdexseβdexsa, βdexsacyclodextrin, cyclodextrinlimonene, limoneneresolution, resolutionβdexsp, βdexspcolumn, columntrans
1-octen-3-ol and carvone - Rt-βDEXsa™
1-octen-3-ol and carvone - Rt-βDEXsa™ 1. (+/-)1-octen-3-ol 2. (-)carvone 3. (+)carvone 2 3 1 min. 20 30 40 GC_FF00151 30m, 0.32mm ID, 0.25µm Rt-βDEXsa™ (cat.# 13108) Oven temp.: 40°C (hold 1 min.) to 230°C @ 2°C/min. (hold 3 min.) Carrier…
Key words
hydrogen
Raspberry Flavor - Rt-βDEXsa™
Raspberry Flavor - Rt-βDEXsa™ 1. (R)-α-ionone 2. (S)-α-ionone 1 2 min. 10 20 30 GC_FF00161 30m, 0.32mm ID, 0.25µm Rt-βDEXsa (cat.# 13108) Oven temp.: 60°C (hold 2 min.) to 200°C @ 3°C/min. Carrier gas: helium; 60cm/sec. set @ 60°C Det.:…
Key words
βdexsa, βdexsaraspberry, raspberryflavor
Other projects
LCMS
ICPMS
Follow us
More information
WebinarsAbout usContact usTerms of use
LabRulez s.r.o. All rights reserved. Content available under a CC BY-SA 4.0 Attribution-ShareAlike