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    <subfield code="a">B-21110</subfield>
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    <subfield code="a">GC-MS AND Chemometric Analysis of the Essential Oils Obtained from Mexican Commercial Chamomilla Recutita Teas</subfield>
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    <subfield code="v">Chemistry &amp; BioDiversity, 19, p.e202400333, 2024</subfield>
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    <subfield code="a">The essential oils prepared by hydrodistillation of twenty-one brands of German chamomile (S1-S21)commercialized in Mexico were analyzed by GS-MS. Altogether, twenty-four different compounds were identified in the analyzed samples, varying from 77 to 100 percent of the total composition. Multivariate analyses were applied to explore similarity/dissimilarity and correlation between all samples; the results revealed a strong correlation among samples S4, S5, and S7-S21 due to the presence of (Z)-en-yn-dicycloether [(Z)-tonghaosu], ?-bisabolol, ?-farnesene, ?-eudesmol, and xanthoxylin. The samples S1-S3 and S6 were clustered separately. Samples S1, S3, and S6 were characterized by their higher content of bisabolol oxide A (38.78 percent, 51.84 percent, and 70.46 percent, respectively)as most known chemotypes of German chamomile, but only S1 and S3 contained chamazulene. Finally, S2 differed from the others because of its high content of (E)-anethole (62.28 percent), suggesting a case of adulteration or substitution of the crude drug employed for manufacturing the product.</subfield>
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    <subfield code="a">MULTIVARIATE ANALYSIS</subfield>
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    <subfield code="a">Mata, R.</subfield>
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    <subfield code="a">P&#xE9;rez-V&#xE1;squez, A.</subfield>
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    <subfield code="u">https://drive.google.com/open?id=1Zxcjib45pYkjWKvA83_Jxv38ZdfSfCOz&amp;usp=drive_copy</subfield>
    <subfield code="z">Para ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx</subfield>
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    <subfield code="c">31126</subfield>
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    <subfield code="d">2025-06-25</subfield>
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    <subfield code="o">B-21110</subfield>
    <subfield code="r">2025-06-25 16:25:01</subfield>
    <subfield code="w">2025-06-25</subfield>
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