Lovastatin EP Impurity D
Synonyms: Lovastatin Dimer · Lovastatin - Impurity D
Lovastatin EP Impurity D (CAS 149756-62-7) – Lovastatin impurity standard. C48H72O10, MW 809.1. Supplied by Vaqora Chemicals with COA, exported worldwide.
About Lovastatin EP Impurity D
Vaqora Chemicals supplies Lovastatin EP Impurity D, a pharmacopeial impurity of Lovastatin registered under CAS number 149756-62-7. Its molecular formula is C48H72O10 and its molecular weight is 809.1 g/mol. It is also known as Lovastatin Dimer or Lovastatin - Impurity D.
It is supplied as a solid. Store the standard in its sealed vial, protected from light and moisture, and follow the storage condition printed on the COA. Good laboratory practice and suitable PPE are recommended during handling.
This Lovastatin impurity supports analytical method development and validation (AMV), batch release testing and the impurity sections of ANDA and DMF filings. Buyers come mainly from pharmaceutical manufacturing and academic and industrial research.
Standard pack sizes are 10 mg, 25 mg, 50 mg and 100 mg, and every batch ships with a Certificate of Analysis (COA) and we export worldwide.
Typical applications
- Pharmacopeial method verification
- Impurity profiling
- QC release testing
- ANDA / DMF filings
Industries
View every impurity, metabolite and intermediate we list for Lovastatin.
Lovastatin impuritiesGrade guides
Specifications & identifiers
| Product name | Lovastatin EP Impurity D |
|---|---|
| Catalogue No. | VQ-031659 |
| CAS Number | 149756-62-7 |
| IUPAC name | [(4R)-2-[2-[(1S,2S,6R,8S,8aR)-2,6-dimethyl-8-[(2S)-2-methylbutanoyl]oxy-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl]-6-oxooxan-4-yl] (3R,5R)-7-[(1S,2S,6R,8S,8aR)-2,6-dimethyl-8-[(2S)-2-methylbutanoyl]oxy-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoate |
| Molecular formula | C48H72O10 |
| Molecular weight | 809.1 g/mol |
| Exact mass | 808.5125 |
| Grade | Reference Standard |
| HSN code | 38229090 |
| InChIKey | GZGUDHDMNATZDU-CRMSOXFQSA-N |
| SMILES | CC[C@H](C)C(=O)O[C@H]1C[C@H](C=C2[C@H]1[C@H]([C@H](C=C2)C)CCC3C[C@H](CC(=O)O3)OC(=O)C[C@@H](C[C@@H](CC[C@H]4[C@H](C=CC5=C[C@@H](C[C@@H]([C@H]45)OC(=O)[C@@H](C)CC)C)C)O)O)C |
| PubChem CID | 71749741 |
| Physical form | Solid |
|---|---|
| LogP (XLogP3) | 8.6 |
| H-bond donors / acceptors | 2 / 10 |
| TPSA | 146 Ų |
Documents
Frequently asked questions
What is the CAS number of Lovastatin EP Impurity D?
The CAS Registry Number of Lovastatin EP Impurity D is 149756-62-7. It is also known as Lovastatin Dimer, Lovastatin - Impurity D.
What is the molecular formula and molecular weight of Lovastatin EP Impurity D?
Lovastatin EP Impurity D has the molecular formula C48H72O10 and a molecular weight of 809.1 g/mol.
What is Lovastatin EP Impurity D used for?
Lovastatin EP Impurity D is supplied as a characterised reference material related to Lovastatin. It is used for analytical method development and validation (AMV), impurity profiling, stability studies and quality control, and in ANDA/DMF regulatory filings.
Which grade and pack sizes of Lovastatin EP Impurity D can I order?
We supply Lovastatin EP Impurity D in Reference Standard grade, in 10 mg, 25 mg, 50 mg, 100 mg packs. Larger bulk quantities and custom packing are quoted on request.
Do you provide a COA and SDS with Lovastatin EP Impurity D?
Yes. Every lot of Lovastatin EP Impurity D is shipped with a batch-specific Certificate of Analysis, and a 16-section GHS Safety Data Sheet is provided with the quotation and the shipment.
Can Lovastatin EP Impurity D be shipped internationally?
Yes. We export Lovastatin EP Impurity D worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.
Enquire about Lovastatin EP Impurity D
We reply within one business day with price, pack options, lead time and documentation.