Raltegravir EP Impurity E
Synonyms: Raltegravir Related Compound E USPRS · Raltegravir - Impurity E · 4-Defluoro raltegravir · Raltegravir Related Compound E
Raltegravir EP Impurity E (CAS 1193687-87-4) – Raltegravir impurity standard. C20H22N6O5, MW 426.4. Order from Vaqora Chemicals with COA and global delivery.
About Raltegravir EP Impurity E
Vaqora Chemicals supplies Raltegravir EP Impurity E, a pharmacopeial impurity of Raltegravir registered under CAS number 1193687-87-4. Formula C20H22N6O5, molecular weight 426.4 g/mol. Common synonyms include Raltegravir Related Compound E USPRS and Raltegravir - Impurity E.
It is supplied as a solid. Keep the vial tightly closed, protected from light and humidity, at the temperature stated on the Certificate of Analysis. Good laboratory practice and suitable PPE are recommended during handling.
As a characterised impurity of Raltegravir, it is used for analytical method development, method validation (AMV) and routine quality-control testing, and it supports ANDA and DMF regulatory filings. 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 Raltegravir.
Raltegravir impuritiesGrade guides
Specifications & identifiers
| Product name | Raltegravir EP Impurity E |
|---|---|
| Catalogue No. | VQ-023606 |
| CAS Number | 1193687-87-4 |
| IUPAC name | N-[2-[4-(benzylcarbamoyl)-5-hydroxy-1-methyl-6-oxopyrimidin-2-yl]propan-2-yl]-5-methyl-1,3,4-oxadiazole-2-carboxamide |
| Molecular formula | C20H22N6O5 |
| Molecular weight | 426.4 g/mol |
| Exact mass | 426.1652 |
| Grade | Reference Standard |
| HSN code | 38229090 |
| InChIKey | COAAUZDDPLHEFT-UHFFFAOYSA-N |
| SMILES | CC1=NN=C(O1)C(=O)NC(C)(C)C2=NC(=C(C(=O)N2C)O)C(=O)NCC3=CC=CC=C3 |
| PubChem CID | 137552082 |
| Physical form | Solid |
|---|---|
| LogP (XLogP3) | 1 |
| H-bond donors / acceptors | 3 / 8 |
| TPSA | 150 Ų |
| Synonyms | Raltegravir Related Compound E USPRS, Raltegravir - Impurity E, 4-Defluoro raltegravir, Raltegravir Related Compound E, 4-DefluoroRaltegravir, Raltegravir Impurity G |
Documents
Frequently asked questions
What is the CAS number of Raltegravir EP Impurity E?
The CAS Registry Number of Raltegravir EP Impurity E is 1193687-87-4. It is also known as Raltegravir Related Compound E USPRS, Raltegravir - Impurity E, 4-Defluoro raltegravir.
What is the molecular formula and molecular weight of Raltegravir EP Impurity E?
Raltegravir EP Impurity E has the molecular formula C20H22N6O5 and a molecular weight of 426.4 g/mol. Its IUPAC name is N-[2-[4-(benzylcarbamoyl)-5-hydroxy-1-methyl-6-oxopyrimidin-2-yl]propan-2-yl]-5-methyl-1,3,4-oxadiazole-2-carboxamide.
What is Raltegravir EP Impurity E used for?
Raltegravir EP Impurity E is supplied as a characterised reference material related to Raltegravir. 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 Raltegravir EP Impurity E can I order?
We supply Raltegravir 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 Raltegravir EP Impurity E?
Yes. Every lot of Raltegravir 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 Raltegravir EP Impurity E be shipped internationally?
Yes. We export Raltegravir 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 Raltegravir EP Impurity E
We reply within one business day with price, pack options, lead time and documentation.
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