Skip to Content
Merck
  • Characterization of skin sensitizers from autoxidized citronellol - impact of the terpene structure on the autoxidation process.

Characterization of skin sensitizers from autoxidized citronellol - impact of the terpene structure on the autoxidation process.

Contact dermatitis (2014-03-29)
Johanna Rudbäck, Lina Hagvall, Anna Börje, Ulrika Nilsson, Ann-Therese Karlberg
ABSTRACT

Citronellol is a frequently used fragrance compound in consumer products. It is present in fragrance mix II, which is used for screening of contact allergy to fragrances. Because of its chemical structure, citronellol could be susceptible to autoxidation. To compare the behaviour of citronellol with that of the structurally similar compounds linalool and geraniol, in terms of ability to autoxidize, the products formed, and the sensitization potencies of these. Citronellol was exposed to air, and autoxidation was followed by gas chromatography-mass spectrometry (GC-MS) analysis after derivatization of thermolabile compounds. The sensitizing potencies of the oxidation mixture and its major oxidation compounds were examined with the local lymph node assay. The concentration of citronellol decreased while the sensitization potency increased in air-exposed samples over time, with hydroperoxides being identified as the major oxidation products and main skin sensitizers. The present study shows the impact of the absence of the 2,3-double bond in the citronellol structure on the oxidation pathways for formation of oxidation products. The study also shows the usefulness of our new GC-MS method for quantification of the citronellol oxidation products, especially the hydroperoxides. The investigated citronellol hydroperoxides could be important allergens, owing to the high concentrations detected and frequent exposure to citronellol in the population.

MATERIALS
Product Number
Brand
Product Description

Supelco
N,O-Bis(trimethylsilyl)trifluoroacetamide with trimethylchlorosilane, with 1% trimethylchlorosilane, for GC derivatization, LiChropur
Sigma-Aldrich
Chlorotrimethylsilane, purified by redistillation, ≥99%
Supelco
N,O-Bis(trimethylsilyl)trifluoroacetamide with trimethylchlorosilane, for GC derivatization, LiChropur, contains 10% TMCS, 98% (excluding TMCS)
Supelco
(−)-β-Citronellol, analytical standard
Sigma-Aldrich
Chlorotrimethylsilane, ≥98.0% (GC)
Sigma-Aldrich
Chlorotrimethylsilane, puriss., ≥99.0% (GC)
Supelco
Acetone, analytical standard
Sigma-Aldrich
Chlorotrimethylsilane, produced by Wacker Chemie AG, Burghausen, Germany, ≥99.0% (GC)
Supelco
N,O-Bis(trimethylsilyl)trifluoroacetamide with trimethylchlorosilane, for GC derivatization, LiChropur, contains 1% TMCS, 99% (excluding TMCS)
Sigma-Aldrich
Acetone, natural, ≥97%
Sigma-Aldrich
Acetone, ≥99%, meets FCC analytical specifications
USP
Acetone, United States Pharmacopeia (USP) Reference Standard
Supelco
Acetone, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
Acetone, ACS reagent, ≥99.5%
Supelco
Chlorotrimethylsilane, for GC derivatization, LiChropur, ≥99.0% (GC)
Sigma-Aldrich
Acetone, suitable for HPLC, ≥99.9%
Sigma-Aldrich
Acetone, HPLC Plus, for HPLC, GC, and residue analysis, ≥99.9%
Sigma-Aldrich
Acetone, histological grade, ≥99.5%
Sigma-Aldrich
Acetone, ACS reagent, ≥99.5%
Sigma-Aldrich
1,2,3,5-Tetramethylbenzene, AldrichCPR
Sigma-Aldrich
Citronellol, mixture of isomers, natural, ≥95%, FG
Sigma-Aldrich
Citronellol, ≥95%, FCC, FG
Sigma-Aldrich
N,O-Bis(trimethylsilyl)trifluoroacetamide, ≥99%
Sigma-Aldrich
Chlorotrimethylsilane solution, 1.0 M in THF
Supelco
N,O-Bis(trimethylsilyl)trifluoroacetamide, for GC derivatization, LiChropur, ≥99.0%
Sigma-Aldrich
β-Citronellol, 95%
Supelco
(±)-β-Citronellol, analytical standard