Merck, 8187669011, 2-Propanol

General description
EMPLURA® is our low-cost alternative to high-purity qualities. With EMPLURA we offer a range of solvents for a plurality of basic applications in non-regulated industries and for less demanding applications, preparative laboratory work and cleaning purposes. EMPLURA solvents provide adequate specifications with the most important parameters.
Application

Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones.: The study showcases the role of 2-propanol in asymmetric catalysis, providing an efficient method for the stereoselective hydrogenation of ketones, which is vital in pharmaceutical synthesis (Noyori and Ohkuma, 2001).

Electrospray ionization mass spectrometry of synthetic oligonucleotides using 2-propanol and spermidine.: This research examines the use of 2-propanol in electrospray ionization mass spectrometry, enhancing the detection and analysis of synthetic oligonucleotides (De Bellis et al., 2000).

Isolation, identification, and chemical synthesis of 8 alpha,25-dihydroxy-9,10-seco-4,6,10(19)-cholestatrien-3-one. A new metabolite of 25-hydroxyvitamin D3 produced by mouse myeloid leukemia cells (M1).: This study details the use of 2-propanol in the chemical synthesis of a new vitamin D3 metabolite, which is significant for understanding vitamin D metabolism in leukemia cells (Yamada et al., 1987).

Features and Benefits
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This solvent is safe to use and thus aligns with "Safer Solvents and Auxiliaries". Click here for more information.
Analysis Note
Purity (GC): ≥ 99.5 %
Identity (IR): conforms
Density (d 20 °C/ 4 °C): 0.784 - 0.785
Evaporation residue: ≤ 0.0020 %
Water: ≤ 0.20 %
Legal Information
EMPLURA is a registered trademark of Merck KGaA, Darmstadt, Germany