Direct Calophyllum oil extraction and resin separation with a binary solvent of n-hexane and methanol mixture

This study investigated the use of a mixture of n-hexane and methanol as a binary solvent for the direct oil extraction and resin separation from Calophyllum seeds, in a single step. Optimal oil and resin yields and physicochemical properties were determined by identifying the best extraction conditions. The solvent mixture tested extracted oil and resin effectively from Calophyllum seeds, and separated resin from oil. Extraction conditions affected oil and resin yields and their physicochemical properties, with the n-hexane-to-methanol ratio being the most critical factor. Oil yield improved as n-hexane-to-methanol ratio increased from 0.5:1 to 2:1, and resin yield increased as methanol-to-n-hexane ratio increased from 0.5:1 to 2:1. Physicochemical properties of oil and resin, particularly for acid value and impurity content, improved as the n-hexane-to-methanol ratio decreased from 2:1 to 0.5:1. The best oil (51% with more than 95% triglycerides) and resin (18% with more than 5% polyphenols) yields were obtained with n-hexane-to-methanol ratios of 2:1 and 0.5:1, respectively, at a temperature of 50 °C, with an extraction time of 5 h. The best values for physicochemical property of oil were a density of 0.885 g/cm3, a viscosity of 26.0 mPa.s, an acid value of 13 mg KOH/g, an iodine value of 127 g/100 g, an unsaponifiable content of 1.5%, a moisture content of 0.8% and an ash content of 0.04%

Antimicrobial and cytotoxic agents from Calophyllum inophyllum.

International audienceThe study of the chemical constituents of the root bark and the nut of Calophyllum inophyllum has resulted in the isolation and characterization of a xanthone derivative, named inoxanthone, 3, together with 12 known compounds: caloxanthones A, 4 and B, 5, macluraxanthone, 6, 1,5-dihydroxyxanthone, 7, calophynic acid, 8, brasiliensic acid, 9 inophylloidic acid, 10, friedelan-3-one, 11, calaustralin, 12, calophyllolide, 13, inophyllums C, 14 and E, 15. Their structures were established on the basis of spectral evidence. Their in vitro cytotoxicity against the KB cell line and their antibacterial activity and potency against a wide range of micro organisms were evaluated

A NEW SOURCE OF KOJIC ACID ISOLATED FROM KIGELIA AFRICANA: A POSSIBLE PRECURSOR FOR QUINONE BIOSYNTHESIS

ABSTRACT Kojic acid (5-hydroxy-2-hydroxymethyl-γ-pyrone) a fungal metabolite produced by Aspergillus spp., Penicillium spp. and belonging mainly to the flavus-oryzaetamarii groups was isolated for the first time from Kigelia africana as the major constituent by mass fragmentation guided isolation. From a biosynthetic consideration, Kojic acid is a possible intermediate in the synthesis of the quinone scaffolds