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Dexamethasone Sodium Phosphate EP Impurity G

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COA COO

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Dexamethasone Sodium Phosphate EP Impurity G

Impurity

CAS Number

37927-01-8

Molecular Formula

C21H27FO5

Product format

Neat

Molecular Weight

378.44

USP Description

Fluoroandrostadiene Carboxylic Acid

Storage

+5°C

Shipping

Room Temperature

API Family

Dexamethasone Sodium Phosphate

Synonyms

(11ß, 16a, 17a)-9-Fluoro-11, 17-dihydroxy-16-methyl-3-oxo-androsta-1, 4-diene-17-carboxylic Acid, (-)-Dexamethasone acid, 9-Fluoro-11ß, 17-dihydroxy-16a-methyl-3-oxoandrosta-1, 4-diene-17ß-carboxylic acid, Dexamethasone Sodium Phosphate Imp. G (EP), Dexamethasone Sodium Phosphate Impurity G and Dexamethasone Phosphate Impurity G

Smiles

C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(O)C(=O)O

Iupac Name

(8S, 9R, 10S, 11S, 13S, 14S, 16R, 17R)-9-fluoro-11, 17-dihydroxy-10, 13, 16-trimethyl-3-oxo-6, 7, 8, 11, 12, 14, 15 and 16-octahydrocyclopenta[a]phenanthrene-17-carboxylic acid

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Available products

Pack Size SKU
Category Expected Delivery Price Quantity
10mg
CE4456.11-10MG

3-4 weeks

25mg
CE4456.11-25MG

3-4 weeks

50mg
CE4456.11-50MG

3-4 weeks

100mg
CE4456.11-100MG

3-4 weeks

25mg
CD4456.11-25MG

3-5 weeks

100mg
CD4456.11-4X25MG

3-5 weeks

25mg
CB4456.11-25MG

4-5 weeks

100mg
CB4456.11-4X25MG

4-5 weeks

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Product Type

Impurity

Our Impurity Characterized Standards portfolio comprises more than 5,000 compounds accompanied by a comprehensive CoA which can be found in 3 product categories that include a set of different analytical techniques for determining Identity and Purity.

API

We have designed a range of primary API standards manufactured according to international regulations that come with the most extensive Certificate of Analysis which includes Identity checks by several techniques.

Excipient

Excipients standards comes with a detailed Certificate of Analysis with Identity, Purity and Assay data. They are also suitable for use with non-compendial analytical methods.

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Synthesis

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