Everolimus EP Impurity E
Synonyms: Everolimus - Impurity E
Everolimus EP Impurity E (CAS 1237826-25-3) – Everolimus impurity standard. C52H79NO14, MW 942.2. Supplied by Vaqora Chemicals with COA, exported worldwide.
About Everolimus EP Impurity E
Everolimus EP Impurity E is a pharmacopeial impurity of Everolimus carrying the CAS registry number 1237826-25-3. Formula C52H79NO14, molecular weight 942.2 g/mol. Common synonyms include Everolimus - Impurity E.
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. Handle it with standard laboratory precautions and appropriate personal protective equipment.
Pharmaceutical QC and development laboratories use this impurity standard of Everolimus to develop and validate HPLC methods, to set specification limits and to document impurity profiles in ANDA and DMF submissions. Our customers for this product work in 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 Everolimus.
Everolimus impuritiesGrade guides
Specifications & identifiers
| Product name | Everolimus EP Impurity E |
|---|---|
| Catalogue No. | VQ-030638 |
| CAS Number | 1237826-25-3 |
| IUPAC name | [(1R,2R,4S)-4-[(2R)-2-[(1R,9S,12S,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32S,35R)-1,18-dihydroxy-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-2,3,10,14,20-pentaoxo-11,36-dioxa-4-azatricyclo[30.3.1.04,9]hexatriaconta-16,24,26,28-tetraen-12-yl]propyl]-2-methoxycyclohexyl] formate |
| Molecular formula | C52H79NO14 |
| Molecular weight | 942.2 g/mol |
| Exact mass | 941.5501 |
| Grade | Reference Standard |
| HSN code | 38229090 |
| InChIKey | IUPNCBWADBCXHV-MYYCYPOOSA-N |
| SMILES | C[C@@H]1CC[C@H]2C[C@@H](/C(=C/C=C/C=C/[C@H](C[C@H](C(=O)[C@@H]([C@@H](/C(=C/[C@H](C(=O)C[C@H](OC(=O)[C@@H]3CCCCN3C(=O)C(=O)[C@@]1(O2)O)[C@H](C)C[C@@H]4CC[C@H]([C@@H](C4)OC)OC=O)C)/C)O)OC)C)C)/C)OC |
| PubChem CID | 140569793 |
| Physical form | Solid |
|---|---|
| LogP (XLogP3) | 6.6 |
| H-bond donors / acceptors | 2 / 14 |
| TPSA | 202 Ų |
Documents
Frequently asked questions
What is the CAS number of Everolimus EP Impurity E?
The CAS Registry Number of Everolimus EP Impurity E is 1237826-25-3. It is also known as Everolimus - Impurity E.
What is the molecular formula and molecular weight of Everolimus EP Impurity E?
Everolimus EP Impurity E has the molecular formula C52H79NO14 and a molecular weight of 942.2 g/mol.
What is Everolimus EP Impurity E used for?
Everolimus EP Impurity E is supplied as a characterised reference material related to Everolimus. 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 Everolimus EP Impurity E can I order?
We supply Everolimus EP Impurity E 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 Everolimus EP Impurity E?
Yes. Every lot of Everolimus EP Impurity E 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 Everolimus EP Impurity E be shipped internationally?
Yes. We export Everolimus EP Impurity E worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.
Enquire about Everolimus EP Impurity E
We reply within one business day with price, pack options, lead time and documentation.
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