Y0001555

Ciclesonide impurity B

European Pharmacopoeia (EP) Reference Standard

• Sinónimos: Desisobutyryl-ciclesonide, (2′R)-2′-Cyclohexyl-11b,21-dihydroxy-16bH-[1,3]dioxolo[4′,5′:16,17]pregna-1,4-diene-3,20-dione
• Fórmula empírica (notación de Hill): C₂₈H₃₈O₆
• Número de CAS: 161115-59-9
• Peso molecular: 470.60
• UNSPSC Code: 41116107
• NACRES: NA.24

Propiedades

• biological source: synthetic
• grade: pharmaceutical primary standard
• agency: EP
• API family: ciclesonide
• form: powder
• packaging: pkg of 10 mg
• manufacturer/tradename: EDQM
• storage condition: protect from light
• solubility: water: <0.1 g/L
• application(s): pharmaceutical (small molecule)
• format: neat
• shipped in: ambient
• storage temp.: 2-8°C
• InChI: 1S/C28H38O6/c1-26-11-10-18(30)12-17(26)8-9-19-20-13-23-28(22(32)15-29,27(20,2)14-21(31)24(19)26)34-25(33-23)16-6-4-3-5-7-16/h10-12,16,19-21,23-25,29,31H,3-9,13-15H2,1-2H3/t19-,20-,21-,23+,24+,25+,26-,27-,28+/m0/s1
• InChI key: OXPLANUPKBHPMS-ZXBNPROVSA-N

Descripción

General description

Ciclesonide impurity B is an impurity of ciclesonide, a new-generation, non-halogenated glucocorticoid.
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets, have been developed and issued under the Authority of the issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Ciclesonide impurity B is used as an EP reference standard to quantify the analyte in pharmaceutical formulations by liquid chromatography (LC) technique.

Packaging

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Other Notes

Sales restrictions may apply.