Ephedrine Hydrochloride EP Impurity A

CAS: 1798-60-3

Ref. 3D-IE176322

Produktinformation

• Name: Ephedrine Hydrochloride EP Impurity A
• Synonyme: (1R)-1-Hydroxy-1-phenylpropan-2-one, (-)-(1R)-1-Hydroxy-1-phenyl-2-propanone, (1R)-1-Phenyl-1-hydroxypropan-2-one, (1R)-1-hydroxy-1-phenylpropan-2-one, (R)-1-Hydroxy-1-phenyl-2-propanone, (R)-1-Hydroxy-1-phenylpropanone, (R)-Hydroxy-1-Phenyl-2-propanedione, (R)-Phenylacetylcarbinol, 1-Hydroxy-1-Phenylpropan-2-One, 2-Propanone, 1-hydroxy-1-phenyl-, (1R)-, 2-Propanone, 1-hydroxy-1-phenyl-, (R)-, <span class="text-smallcaps">D</span>-(-)-1-Hydroxy-1-phenylpropanone, <span class="text-smallcaps">D</span>-(-)-1-Phenyl-1-hydroxy-2-propanone, <span class="text-smallcaps">D</span>-(-)-Phenylacetylcarbinol, l-Phenylacetylcarbinol
• CAS: 1798-60-3

Beschreibung

Ephedrine Hydrochloride EP Impurity A is a product of the biotransformations of pseudoephedrine. It has been shown that this impurity can be formed in enzymatic reactions where pseudoephedrine is acted upon by β-unsaturated ketones or by filamentous fungi. Ephedrine Hydrochloride EP Impurity A is a chiral compound, which means that it has two different forms that are non-superimposable mirror images of each other. The enantiomers (left and right) are the individual molecules that make up the racemic mixture. In some cases, ephedrine hydrochloride ep impurity a may be present as a result of a reaction between pseudoephedrine and an enzyme preparation containing β-unsaturated ketones, such as acetone peroxide or benzoyl peroxide. This impurity has been shown to inhibit candida glabrata and to have kinetic properties similar to that of ephed

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 150.17 g/mol
• Formel: C₉H₁₀O₂
• Reinheit: Min. 96 Area-%
• Farbe/Form: Clear Viscous Liquid