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Rivaroxaban Phthalimido Descarbonyl Impurity

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COA COO

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Rivaroxaban Phthalimido Descarbonyl Impurity

Impurity

CAS Number

446292-07-5

Molecular Formula

C21H21N3O5

Product format

Neat

Molecular Weight

395.41

USP Description

Rivaroxaban Phthalimido Analog

Storage

+5°C

Shipping

Room Temperature

API Family

Rivaroxaban

Synonyms

2-[(2R)-2-Hydroxy-3-[[4-(3-oxo-4-morpholinyl)phenyl]amino]propyl]-1H-isoindole-1 and 3(2H)-dione

Smiles

O[C@H](CNc1ccc(cc1)N2CCOCC2=O)CN3C(=O)c4ccccc4C3=O

Iupac Name

2-[(2R)-2-hydroxy-3-[4-(3-oxomorpholin-4-yl)anilino]propyl]isoindole-1 and 3-dione

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COA COO

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Available products

Pack Size SKU
Category Expected Delivery Price Quantity
25mg
CE4220.19-25MG

In Stock(Pending QC - 1-2 weeks)

50mg
CE4220.19-50MG

In Stock(Pending QC - 1-2 weeks)

100mg
CE4220.19-100MG

In Stock(Pending QC - 1-2 weeks)

25mg
CD4220.19-25MG

In Stock(Pending QC - 2-3 weeks)

100mg
CD4220.19-4X25MG

In Stock(Pending QC - 2-3 weeks)

25mg
CB4220.19-25MG

In Stock(Pending QC - 2-3 weeks)

100mg
CB4220.19-4X25MG

In Stock(Pending QC - 2-3 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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