Y0001556
Ciclesonid Unreinheit C
European Pharmacopoeia (EP) Reference Standard
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About This Item
Empfohlene Produkte
Biologische Quelle
synthetic
Qualität
pharmaceutical primary standard
Agentur
EP
API-Familie
ciclesonide
Form
powder
Verpackung
pkg of 10 mg
Hersteller/Markenname
EDQM
Lagerbedingungen
protect from light
Löslichkeit
water: <0.1 g/L
Anwendung(en)
pharmaceutical (small molecule)
Format
neat
Versandbedingung
ambient
Lagertemp.
2-8°C
Allgemeine Beschreibung
Ciclesonide impurity C is an impurity of ciclesonide, which is 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.
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.
Anwendung
Ciclesonide impurity C is used as a EP reference standard to quantify the analyte in pharmaceutical formulations using liquid chromatography (LC) technique.
Verpackung
The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.
Sonstige Hinweise
Sales restrictions may apply.
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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Analysenzertifikate (COA)
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Ciclesonide
European pharmacopoeia, 10.3 (2017)
Clinical pharmacokinetics, 43(7), 479-486 (2004-05-14)
Ciclesonide is a novel inhaled corticosteroid developed for the treatment of asthma. To investigate the extent of oral absorption and bioavailability of ciclesonide referenced to an intravenous infusion. This information provides an estimate for the contribution of the swallowed fraction
New Drugs for Asthma, Allergy and COPD (2001)
Rethinking Cleaning Validation for API Manufacturing
Pharmaceutical Technology, 42, 42-54 (2018)
Pharmacokinetics of [14 C] ciclesonide after oral and intravenous administration to healthy subjects
Clinical Pharmacokinetics, 43, 479-486 (2004)
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