Y0001555

Ciclesonide impurity B

European Pharmacopoeia (EP) Reference Standard

• 別名: Desisobutyryl-ciclesonide, (2′R)-2′-Cyclohexyl-11b,21-dihydroxy-16bH-[1,3]dioxolo[4′,5′:16,17]pregna-1,4-diene-3,20-dione
• 実験式（ヒル表記法）: C₂₈H₃₈O₆
• CAS番号: 161115-59-9
• 分子量: 470.60
• UNSPSCコード: 41116107
• NACRES: NA.24

特性

• 由来生物: synthetic
• グレード: pharmaceutical primary standard
• 認証: EP
• APIファミリー: ciclesonide
• 形状: powder
• 包装: pkg of 10 mg
• メーカー／製品名: EDQM
• 保管条件: protect from light
• 溶解性: water: <0.1 g/L
• アプリケーション: pharmaceutical (small molecule)
• フォーマット: neat
• 輸送温度: ambient
• 保管温度: 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 Key: OXPLANUPKBHPMS-ZXBNPROVSA-N

詳細

詳細

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.

アプリケーション

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

包装

この製品は発行元の薬局方による供給としてお届けします。現在の単位量については、EDQM reference substance catalogueをご覧ください。

その他情報

Sales restrictions may apply.