2015
DOI: 10.1021/ed500788q
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Determination of Niacinamide in Lotions and Creams Using Liquid–Liquid Extraction and High-Performance Liquid Chromatography

Abstract: Chemical separations are an important part of an undergraduate chemistry curriculum. Sophomore students often get experience with liquid−liquid extraction in organic chemistry classes, but liquid−liquid extraction is not as often introduced as a quantitative sample preparation method in honors general chemistry or quantitative analysis classes. This experiment offers a relevant, interesting way to use liquid−liquid extraction and high-performance liquid chromatography (HPLC) to analyze popular lotions and crea… Show more

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Cited by 12 publications
(12 citation statements)
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“…All chemicals used were of either analytical or pharmaceutical grade. 12 10 mg of Niacinamide was accurately weighed and transferred into 10 ml clean dry volumetric flask; 7 ml of water was added and sonicated for 5 mins. Finally, the volume was made up to 10 ml with water.…”
Section: Materials and Methods Materialsmentioning
confidence: 99%
“…All chemicals used were of either analytical or pharmaceutical grade. 12 10 mg of Niacinamide was accurately weighed and transferred into 10 ml clean dry volumetric flask; 7 ml of water was added and sonicated for 5 mins. Finally, the volume was made up to 10 ml with water.…”
Section: Materials and Methods Materialsmentioning
confidence: 99%
“…While the procedure itself is of moderate complexity for the novice organic chemistry student, the underlying concepts and their interconnectedness provide a more nuanced opportunity to probe student understanding of solubility/miscibility, density, and acid–base chemistry. In the classic liquid–liquid extraction separation procedure, two components (or more) are separated by using base to selectively deprotonate one component rendering it soluble in water while the other component remains soluble in the organic phase. After separation of the phases, the aqueous phase is then acidified, reprotonating the water-soluble conjugate base to yield an insoluble material that can be removed by filtration or by extraction with an organic phase. Alternately, a component that readily protonates may be extracted into an aqueous phase using acid, and then base to return the component to the organic phase.…”
Section: Introductionmentioning
confidence: 99%
“…Depending on the pH of the aqueous solution and the p K a of different functional groups, molecules will exist in their ionic or nonionic states and dissolve better in either the aqueous or organic layer (Figure ). Although there have been several laboratory experiments designed to teach students this technique, beginning students of organic chemistry continue to struggle to connect the concepts involved in acid–base extraction . Therefore, additional methods such as demonstrations should be implemented to increase and support students’ learning.…”
Section: Introductionmentioning
confidence: 99%