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Boron trifluoride methanol bf3

Manufactured by Merck Group
Sourced in France, Portugal

Boron trifluoride-methanol (BF3) is a chemical compound commonly used as a laboratory reagent. It is a colorless, volatile liquid with a pungent odor. BF3 is a Lewis acid and is used in various organic synthesis reactions, particularly in the areas of electrophilic addition and rearrangement reactions.

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2 protocols using boron trifluoride methanol bf3

1

Enzymatic Hydrolysis of Salmon Lecithin

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Salmon lecithin was obtained by enzymatic hydrolysis in our laboratory, as described before [23 (link)]. Lipidic fractions were extracted by a low temperature enzymatic process that is solvent-free. The following materials were used in the present study: acetonitrile and diethyl ether (Sigma-Aldrich, Lyon, France), boron trifluoride-methanol (BF3) (Supelco, Bellfonte, PA, USA), chloroform (VWR-Prolabo, Milan, Italy), hexane, methanol, and formic acid (Carlo-Erba, Peypin, France), and ammoniac (Merck KGaA, Darmstadt, Germany). All of the organic solvents used were analytical grade reagents.
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2

Fatty Acid Analysis by GC-FID

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Sodium hydroxide and anhydrous sodium sulfate were obtained from Pronalab (Lisbon, Portugal); boron trifluoride-methanol (BF3) (14% in methanol), Supelco 37 Component FAME Mix and butylated hydroxytoluene (BHT) (≥99%) were from Sigma-Aldrich (St. Louis, MI, USA); dichloromethane, methanol and n-hexane (99%) were from Merck (Darmstadt, Germany); Tridecanoic acid (C13:0) was from Fluka (Buchs, Switzerland) and sodium chloride (99.5%) was from Panreac (Barcelona, Spain).
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