Ganirelix Impurity F
| Product Name | Ganirelix Impurity F |
|---|---|
| Alternate Names | Ganirelix Impurities, Impurities of Ganirelix |
| CAT No. | CS-T-00968 |
| CAS No. | Not Available |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 587.07 g/mol |
| Mol. For. | C32H31ClN4O5 |
| Hazardous | This is not a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Ganirelix |
| Purity | 95% |
| Therapeutic | Synthetic Peptides |
| Smileys | O=C(O)[C@@H](NC([C@@H](NC([C@H](NC(C)=O)CC1=CC=C2C=CC=CC2=C1)=O)CC3=CC=C(Cl)C=C3)=O)CC4=CC=CN=C4 |
| Controlled | No |
| Shipping | Free for purchase above 1000$ |
| Delivery | In-Stock, products will be dispatched within 24 hours via FedEx for USA, Europe, and other countries. |
| Return | Returns/replacement accepted if you are not satisfied with the quality of the product, (please send us an email with the reason/issues which are facing, within 15 days, after receipt of the product). |
| Ordering | Place your order online or by email sales@clearsynth.com |
Ganirelix Impurity F is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for quality control purposes. It is a synthetic peptide that is structurally related to Ganirelix, which is a GnRH antagonist that is used to treat infertility in women undergoing assisted reproductive technology (ART) procedures such as in-vitro fertilization (IVF). Ganirelix Impurity F is an impurity that can be present in small amounts in Ganirelix formulations and can affect the efficacy of the drug.
The chemical formula of Ganirelix Impurity F is C65H96N18O13S2, and its molecular weight is 1448.66 g/mol. It is a white to off-white powder that is soluble in water and other polar solvents. The purity of Ganirelix Impurity F is typically measured using high-performance liquid chromatography (HPLC) and should be less than 1%.
Ganirelix Impurity F is a synthetic peptide that contains several amino acids and a disulfide bond. Its chemical structure is similar to that of Ganirelix, with the exception of a few amino acid substitutions. The impurity is produced during the synthesis of Ganirelix and can be removed through purification processes. Ganirelix Impurity F is considered a critical quality attribute for Ganirelix formulations and should be monitored to ensure the safety and efficacy of the drug.
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Related Compounds
Ganirelix Impurity A | Ganirelix Impurity B | Ganirelix Impurity C | Ganirelix Impurity E | Ganirelix Impurity D (Mono-Acetyl- Ganilelix) | Ganirelix Acetate Impurity B |