Accéder au contenu
Merck

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
RÉSUMÉ

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.

MATÉRIAUX
Référence du produit
Marque
Description du produit

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