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BRAND

Ketorolac EP Impurity I

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COA COO

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Ketorolac EP Impurity I

Impurity

CAS Number

113502-55-9

Molecular Formula

C14H13NO

Product format

Neat

Molecular Weight

211.26

USP Description

Ketorolac Related Compound D

Storage

+5°C

Shipping

Room Temperature

API Family

Ketorolac Trometamol

Synonyms

Ketorolac USP Related Compound D, Ketorolac USP RC D, Phenyl(2, 3-dihydro-1H-pyrrolizin-5-yl)methanone, Ketorolac Trometamol Imp. I (EP), Ketorolac Related Compound D, Ketorolac Trometamol Impurity I and Ketorolac Impurity I

Smiles

O=C(c1ccccc1)c2ccc3CCCn23

Iupac Name

6 and 7-dihydro-5H-pyrrolizin-3-yl(phenyl)methanone

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COA COO

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Available products

Pack Size SKU
Category Expected Delivery Price Quantity
2.5mg
CE3354.12-2.5MG

3-4 weeks

20mg
CE3354.12-20MG

3-4 weeks

25mg
CE3354.12-25MG

3-4 weeks

50mg
CE3354.12-50MG

3-4 weeks

100mg
CE3354.12-100MG

3-4 weeks

25mg
CD3354.12-25MG

3-5 weeks

100mg
CD3354.12-4X25MG

3-5 weeks

25mg
CB3354.12-25MG

4-5 weeks

100mg
CB3354.12-4X25MG

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

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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