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Decanoic

Manufactured by Merck Group
Sourced in United Kingdom

Decanoic is a straight-chain saturated fatty acid with the chemical formula CH3(CH2)8COOH. It is a colorless liquid with a mild odor. Decanoic acid is commonly used as a laboratory reagent and in the production of various chemicals and materials.

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3 protocols using decanoic

1

Enzymatic Biocatalysis with Immobilized CALB

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CALB immobilised in acrylic resin (EC 3.1.1.3, 10,000 U/g) (Novozyme 435), xanthine oxidase from bovine milk, xanthine, allopurinol, hesperidin, naringin, and rutin standards and hexanoic, octanoic, decanoic, lauric, and oleic acids were obtained from the Sigma-Aldrich Chemical Co., St. Louis, MO. All the solvents and reagents were of analytical, spectrometric, or chromatographic quality.
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2

Electrospun Fatty Acid-Loaded Polymer Patches

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Electrospinning
methods including solution preparation and patch
production for both PCL and PVP/RS100 patches were performed as previously
described by Santocildes et al.(23 (link)) Briefly, PCL (Mw 80 kDa; Sigma-Aldrich,
Poole, UK) was added at 10 wt % to a solution of dichloromethane/N,N-dimethylformamide (93:7 w/w %; Thermo
Fisher Scientific, Altrincham, UK) and mixed at room temperature until
dissolved. PVP (Kollidon 90 F, Mw 1000–1500
kDa; BASF, Cheadle, UK) at 10 wt % and Eudragit RS100 (Mw 32 kDa; Evonik Industries AG, Essen, Germany) at 12.5
wt % were dissolved in 97% w/w ethanol prepared in deionized water
at room temperature. In this study, short-to-medium-chain fatty acids
including butanoic (C5), hexanoic (C6), heptanoic (C7), octanoic (C8),
nonanoic (C9), decanoic (C10), undecanoic (C11), or dodecanoic (C12)
(all from Sigma-Aldrich, Poole, UK) were added to the polymer dope
solutions at a concentration of 0.2 M prior to spinning. Spinning
conditions were 17 kV, 3 mL/h with a 15 cm tip-to-collector distance. 1H NMR spectroscopy was used to show that solvents were absent
in the final composition of patches (Figure S1).
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3

Fatty Acid Hydrogenation and Acetylation

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Chemicals were purchased from Sigma-Aldrich (Brazil and Canada). Decanoic, myristic, stearic, and oleic acids were purchased from Sigma-Aldrich. Cardanol mixture was donated by Resibras/Cashol (Fortaleza, Brazil). Hydrogenation were performed in a shaker hydrogenation apparatus (Paar Instruments). The acetylation reactions were performed in a household microwave Brastemp BMK38ABHNA model and power 900 W. Chromatographic separations were performed using silica gel columns by flash (silica gel 60, 230â€"400 and 70â€"230 mesh, Silicycle) chromatography with the solvent
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