01834nam a2200205Ia 4500003001000000005001700010040000900027245011500036490005300151520109000204650001001294650002401304650001501328650002601343700001301369700002601382700002501408856015401433008004101587MX-MdCICY20260521091753.0  cCICY10aGC-MS AND Chemometric Analysis of the Essential Oils Obtained from Mexican Commercial Chamomilla Recutita Teas0 vChemistry & BioDiversity, 19, p.e202400333, 20243 aThe 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.14aGC-MS14aMATRICARIA RECUTITA14aMANZANILLA14aMULTIVARIATE ANALYSIS12aMata, R.12aPérez-Vásquez, A.12aPeña-Álvarez, A.40uhttps://drive.google.com/open?id=1Zxcjib45pYkjWKvA83_Jxv38ZdfSfCOz&usp=drive_copyzPara ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx250602s9999    xx |||||s2   |||| ||und|d