Cefmepidium chloride

Reagent used for fluorescent labeling of proteins, N-terminal amino acids, and amines. Biochem/physiol Actions Cell permeable: no Primary Target Reagent used for fluorescent labeling of proteins, N-terminal amino acids, and amines Product does not

Didymium oxide (4%) in 10% v/v perchloric acid. Sealed in a far UV quartz cell for wavelength scale accuracy. For both UV and visible region of the spectrum.

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 1.

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 1.

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 1.

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 1.

Packaging This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service .

Diethylaluminum chloride is an organoaluminum reagent used in the reductive condensation of &#945-haloketones. Application Lewis-acid catalyst in Diels-Alder reactions and reactant in the synthesis of aluminum-phosphorus compounds.

Diethylaluminum chloride solution

Application Diethylaluminum chloride solution can be used: As a Lewis acid for the synthesis of Lewis acid-base bifunctional asymmetric catalysts for cyanosilylation of aldehydes and in Strecker reaction. For the synthesis of precursors for

Application Diethylaluminum chloride solution can be used: As a Lewis acid for the synthesis of Lewis acid-base bifunctional asymmetric catalysts for cyanosilylation of aldehydes and in Strecker reaction. For the synthesis of precursors for

Application Diethylaluminum chloride solution can be used: As a Lewis acid for the synthesis of Lewis acid-base bifunctional asymmetric catalysts for cyanosilylation of aldehydes and in Strecker reaction. For the synthesis of precursors for