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The use of hemp (Cannabis sativa L.) essential oil (EO) has shown a significant increase in interest and use during recent years. In this work, a new and simple reversed-phase HPLC with photodiode-array (PDA) detector method has been developed and optimized for the detection and quantification of cannabidiolic acid (CBDA), cannabidiol (CBD), cannabinol (CBN), Δ9-tetrahydrocannabinol (Δ9-THC), and Δ9-tetrahydrocannabinolic acid (THCA). The cannabinoids were extracted from the EO by partition with n-hexane and water, followed by sonication, evaporation to dryness under nitrogen, and reconstitution with methanol:chloroform (9:1, v/v) before HPLC-PDA analysis. The method shows good selectivity and robustness, linearity in the range 0.5–100 mg L−1 with R2 higher than 0.999 for all cannabinoids analyzed, LOD of 0.11–0.16 mg L−1, and LOQ of 0.35–0.48 mg L−1. The recovery was between 78 and 100% and the intra-day and intermediate precision, expressed as relative standard deviation (RSD), was < 4% and 4–10%, respectively. [ABSTRACT FROM AUTHOR]

The composition of the surface waxes of three apple ( Malus domestica L.) cultivars ("Florina", "Golden B" and "Ozark Gold") has been studied by means of spectroscopic and GC–MS analysis of the class-fractionated mixture of components. Odd n -alkanes, mainly C27 and C29 molecules, are prevalent in the saturated fraction. Small concentrations of alkenes were also found; the C28:1 component is strongly (72%) in excess over the other 1-alkenes. Straight-chain esters (mainly of palmitic acid) of saturated primary alcohols (C18–C30) were also detected; whereas the acyl moiety is made up essentially of an even number of carbons, the alcohol counterpart does not exhibit this characteristic. Aldehydes are present (C20–C30) with the homologue patterns C26–C30 most strongly represented. Straight-chain free secondary alcohols characterize the waxes of "Florina" and "Ozark Gold"; the hydroxy function is located far from the extremity of the carbon framework. Outstanding is the presence of three alcohols with 29 carbon centres. These alcohols are accompanied by free straight-chain primary alcohols, mainly with even-numbered carbon chains in the range C26–C30. Free fatty acids are present; all of have a framework of even-numbered carbon chains mainly in the range C16–C20. C18:1 (oleic acid) is well represented. [ABSTRACT FROM AUTHOR]

Analysis of the acid content of coffee extracts has been performed by adaptation of a procedure, recently introduced by our laboratory, to the task of evaluating both the "volatile" and "non volatile" fractions. Besides useful changes in the preparation of the acid pool, diazobutane was used to obtain esters of volatile acids suitable for GC–MS analysis, to minimize losses of material by evaporation. The new procedures have been used to evaluate changes in the acid content of some Italian-style roasted coffee extracts after accelerated ageing (65 °C, 72 h) and in coffee beans after different amounts of roasting. The origin of formation of volatile acidity was also investigated. Electronic supplementary material is available if you access this article at http://dx.doi.org/10.1007/s00216-002-1561-y On that page (frame on the left side) a link takes you directly to the supplementary material. [ABSTRACT FROM AUTHOR]

The nitration of diphenylmethane to three main isomeric dinitro derivatives, performed with nitric acid in dichloromethane, is proposed as an organic laboratory experiment showing a number of advantages over typical aromatic nitrations in sulfuric acid. [ABSTRACT FROM AUTHOR]