Active ingredientFluvastatin Sodium SaltCat. No. P-F106-001CAS 93957-55-2
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Pharmacopoeial impurity · Fluvastatin family
Pharmaceutical analytical standardFluvastatin EP Impurity B (as Racemate)
Synonyms: Fluvastatin t-butyl ester, (+)-
- Cat. No.
- P-F106-003
- CAS
- 129332-29-2
- Alternative CAS
- N/A
- Formula
- C28H34FNO4
- Molecular weight
- 467.58 g/mol
- Category
- Pharmacopoeial impurity (EP/USP)
Family: Fluvastatin
A statin, that is an inhibitor of HMG-CoA reductase, the key enzyme in cholesterol production, in use since the 1990s to lower LDL cholesterol and cardiovascular risk.
Did you know?It was the first entirely synthetic statin: the earlier ones, such as lovastatin, simvastatin and pravastatin, derive from substances made by fungi.
The two levels compared
| Level 1 Mass balance | Level 2 Mass balance + qNMR | |
|---|---|---|
| Identity (IR, MS, 1H and 13C-NMR; peptides: ESI-MS, MALDI-TOF and IR) | ✓ | ✓ |
| HPLC purity (min. 95%) | ✓ | ✓ |
| Content by mass balance (min. 90%; peptides: for information only)* | ✓ | ✓ |
| Content verified by qNMR (small molecules only) | · | ✓ |
| Suitable to qualify it as an in-house primary standard (ICH Q7) | · | ✓ |
* Mass balance is performed on every molecule. The only exceptions are cases where the chemistry of the molecule prevents it, for example oils and highly volatile substances, on which some of the required measurements cannot be made: in those cases the CoA states how the content was assigned.
What you receive
The analytical standard
Shipped under controlled temperature when the molecule requires it.
Certificate of analysis (CoA)
For every lot: identity, purity and assay, with the supporting spectra and chromatograms.
Safety data sheet (SDS)
Sent with every order.
Tracked shipment
Follow your shipment live, from our warehouse to your lab.
More products in the Fluvastatin family
Active ingredientFluvastatin Sodium SaltCat. No. P-F106-001CAS 93957-55-2
Pharmacopoeial impurityFluvastatin EP Impurity A Sodium SaltCat. No. P-F106-002CAS 93957-58-5
Pharmacopoeial impurityFluvastatin EP Impurity BCat. No. P-F106-004CAS 194934-96-8
Pharmacopoeial impurityFluvastatin EP Impurity CCat. No. P-F106-005CAS 2451176-31-9
Pharmacopoeial impurityFluvastatin EP Impurity C Enantiomer Sodium SaltCat. No. P-F106-006
Pharmacopoeial impurityFluvastatin EP Impurity DCat. No. P-F106-008CAS 1160169-39-0
Pharmacopoeial impurityFluvastatin EP Impurity F Sodium SaltCat. No. P-F106-010CAS 2118370-51-5
Pharmacopoeial impurityFluvastatin EP Impurity GCat. No. P-F106-011CAS 101125-34-2Frequently asked questions
Is mass balance always performed?
Yes, on every molecule. The only exceptions are cases where the chemistry of the molecule prevents it: for example oils and highly volatile substances, on which some measurements (such as thermogravimetry) cannot be made. In those cases the CoA states which method was used to assign the content.
Can I ask for a different quantity?
Yes. The quantities are only suggestions: choose "Other" and enter the milligrams or grams you need.
Which level should I choose?
Level 1 is enough for most routine testing. Level 2 adds an independent qNMR content value and is meant for labs that need to qualify an in-house primary standard. For peptides and similar molecules, Level 2 is not available.
When will I get the quote?
Within 24 working hours, with price, availability and delivery time.
Need a molecule you cannot find?
Custom synthesis of impurities, metabolites and labelled compounds, with the same characterisation level.