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Cat. No.: HY-135381

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3-Oxo Atorvastatin

3-Oxo Atorvastatin is an impurity of 3-Oxo Atorvastatin. Atorvastatin is an orally active HMG-CoA reductase inhibitor and has the ability to effectively decrease blood lipids.

For research use only. We do not sell to patients.

CAS No.: 887196-30-7
Formula: C₃₃H₃₃FN₂O₅
Molecular Weight:556.62

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (270 KB)

3-Oxo Atorvastatin Chemical Structure

CAS No.: 887196-30-7

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Top Publications Citing

Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity

Description

3-Oxo Atorvastatin is an impurity of 3-Oxo Atorvastatin. Atorvastatin is an orally active HMG-CoA reductase inhibitor and has the ability to effectively decrease blood lipids^[1].

Chemical Information

CAS No. 887196-30-7
Molecular Weight 556.62
Formula C₃₃H₃₃FN₂O₅
SMILES

O=C(C1=C(C(C)C)N(CC[C@@H](O)CC(CC(O)=O)=O)C(C2=CC=C(F)C=C2)=C1C3=CC=CC=C3)NC4=CC=CC=C4
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (270 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Ramesha, B., et al. DEVELOPMENT AND VALIDATION OF A STABILITY-INDICATING GRADIENT RP-UHPLC METHOD FOR THE DETERMINATION OF IMPURITIES IN ATORVASTATIN DRUG SUBSTANCE. Journal of Liquid Chromatography & Related Technologies.2013; 37(3), 275–297.

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Keywords

100 mg

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