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4 protocols using germacrene d

1

Antioxidant Activity of Plant Extracts

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The standard substances α-pinene (98%), sabinene (95%), p-cymene (99%), limonene (97%), linalool (97%), γ-terpinene (96%), (E)-β-caryophyllene (98.5%), germacrene D (90%), α-humulene (96%), caryophyllene oxide (95%) (98%), p-hydroxybenzoic acid (99%), caffeic acid (98%), o-hydroxybenzoic acid (99%), rosmarinic acid (97%), rutin (94%), AAPH (97%), and fluorescein (99%) were purchased from Sigma Aldrich (St. Louise, MO, USA), and luteolin-7-O-glucoside (98%), kaempferol-3-O-rutinoside (98%), and salvigenin (98%) were purchased from ChemFaces (Wuhan, China); vitexin (≥95%) was purchased from PhytoLab GmbH (Vestenbergsgreuth, Bavaria, Germany). Solvents and other reagents used in the extraction process, GC/FID grade dichloromethane, ammonium formate (99%), 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), formic acid HPLC grade, potassium persulfate (99%), and absolute ethanol (96%) were purchased from Merck (Darmstadt, Germany); commercial ethanol (96%) was acquired from SUQUIN (Bucaramanga, Santander, Colombia).
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2

GC/MS Analysis of Compounds in Essential Oils

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The GC/MS analyses were performed on a Agilent Technologies 7890A Gas Chromatograph, equipped with a HP 5MS 30 m × 0.25 mm × 0.25 μm film thickness capillary column, connected with an Agilent 5957C, VL MS Detector with Triple-Axis Detector system operating in EI mode, and He as the carrier gas (1 mL/min). The initial column temperature was 60°C and heated gradually to 280°C with a 3°C/min rate. The identification of the compounds was based on comparison of their Retention Indices (RI) obtained, using various n-alkanes (C9–C24) and their EI-mass spectra were compared with the NIST/NBS, Wiley libraries spectra, and literature [19 , 20 ]. Additionally, the identity of the indicated phytochemicals was confirmed by comparison with available authentic samples. All authentic samples utilized for the identification of EOs compounds were obtained from Sigma-Aldrich, except for germacrene D and α-thujene, which had been isolated in the context of previous studies.
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3

Comprehensive Phytochemical Profiling of Extracts

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All the chemicals and reagents involved in the extraction processes, total polyphenolic content, antioxidant activity experiments and the chemical standards (1-hexanol, 2-Thujene, 3-octanone, 5-Amino-1-ethylprazole, Allylbenzene, Camphene, Caryophyllene oxide, Decanoic acid, Docosane, Germacrene D, Hexadecane, HexaDecanoic acid, Lavandulol, Limonene, Linalool, Linalool acetate, Nerol, Nerolidol, Ninanal, TetraDecanoic acid, Tricosane, α-Copaene, α-Humulene, α-Ter-pinene, β-Bourbonene, β-Caryophyllene, β-Copaene, β-Cubenene, β-Farnesene, β-Gurjunene, β-Myrcene, β-Pinene) used in the identification of phenolic and aromatic compounds from the extracts were acquired from Sigma Aldrich Company (St. Louis, MO, USA).
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4

Antioxidant Activity of Plant Extracts

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The standard substances α-pinene (98%), sabinene (95%), p-cymene (99%), limonene (97%), linalool (97%), γ-terpinene (96%), (E)-β-caryophyllene (98.5%), germacrene D (90%), α-humulene (96%), caryophyllene oxide (95%) (98%), p-hydroxybenzoic acid (99%), caffeic acid (98%), o-hydroxybenzoic acid (99%), rosmarinic acid (97%), rutin (94%), AAPH (97%), and fluorescein (99%) were purchased from Sigma Aldrich (St. Louise, MO, USA), and luteolin-7-O-glucoside (98%), kaempferol-3-O-rutinoside (98%), and salvigenin (98%) were purchased from ChemFaces (Wuhan, China); vitexin (≥95%) was purchased from PhytoLab GmbH (Vestenbergsgreuth, Bavaria, Germany). Solvents and other reagents used in the extraction process, GC/FID grade dichloromethane, ammonium formate (99%), 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), formic acid HPLC grade, potassium persulfate (99%), and absolute ethanol (96%) were purchased from Merck (Darmstadt, Germany); commercial ethanol (96%) was acquired from SUQUIN (Bucaramanga, Santander, Colombia).
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