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Levonorgestrel EP Impurity Q

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COA COO

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Levonorgestrel EP Impurity Q

Impurity

CAS Number

14507-49-4

Molecular Formula

C20H30O2

Product format

Neat

Molecular Weight

302.46

Shipping

Room Temperature

API Family

Levonorgestrel

Synonyms

(8R, 9S, 13S, 14S, 17S)-13-ethyl-3-methoxy-4, 6, 7, 8, 9, 11, 12, 13, 14, 15, 16 and 17-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol

Iupac Name

13-ethyl-3-methoxy-1, 4, 6, 7, 8, 9, 11, 12, 14, 15, 16 and 17-dodecahydrocyclopenta[a]phenanthren-16-ol

InChI

InChI=1S/C20H30O2/c1-3-20-9-8-17-16-7-5-15(22-2)10-13(16)4-6-18(17)19(20)11-14(21)12-20/h5,14,17-19,21H,3-4,6-12H2,1-2H3

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COA COO

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Available products

Pack Size SKU
Category Expected Delivery Price Quantity
25mg
CE4386.32-25MG

3-4 weeks

25mg
CD4386.32-25MG

3-5 weeks

25mg
CB4386.32-25MG

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

We offer tailor-made synthesis services of up to gram-quantities of materials for a wide range of pharmaceutical customers. The customer can order a specific molecule that is only synthesized on your request on the scale, with the purity and with the specification or methods you require.

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