Y0001555

Ciclesonide impurity B

European Pharmacopoeia (EP) Reference Standard

• 别名: Desisobutyryl-ciclesonide, (2′R)-2′-Cyclohexyl-11b,21-dihydroxy-16bH-[1,3]dioxolo[4′,5′:16,17]pregna-1,4-diene-3,20-dione
• 经验公式（希尔记法）: C₂₈H₃₈O₆
• CAS号: 161115-59-9
• 分子量: 470.60
• 分類程式碼代碼: 41116107
• NACRES: NA.24

属性

• 生物源: synthetic
• 等級: pharmaceutical primary standard
• agency: EP
• API 家族: ciclesonide
• 形狀: powder
• 包裝: pkg of 10 mg
• 製造商／商標名: EDQM
• 儲存條件: protect from light
• 溶解度: water: <0.1 g/L
• 應用: pharmaceutical (small molecule)
• 格式: neat
• 運輸包裝: ambient
• 儲存溫度: 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 密鑰: OXPLANUPKBHPMS-ZXBNPROVSA-N

说明

一般說明

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.

應用

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

包裝

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

其他說明

Sales restrictions may apply.