Levothyroxine EP Impurity B
| Product Name | Levothyroxine EP Impurity B |
|---|---|
| Alternate Names | Levothyroxine Impurities, Impurities of Levothyroxine |
| CAT No. | CS-O-15811 |
| CAS No. | 1628720-66-0 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 685.42 g/mol |
| Mol. For. | C₁₅H₁₁ClI₃NO₄ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Levothyroxine |
| Smileys | IC1=C(OC2=CC(Cl)=C(C(I)=C2)O)C(I)=CC(C[C@@H](C(O)=O)N)=C1 |
| 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 |
Levothyroxine EP Impurity B is a chemical compound that is mainly used in the pharmaceutical industry for quality control purposes. It is a known impurity in the synthesis of Levothyroxine, a hormone medication used to treat thyroid hormone deficiency. The impurity is typically present in small amounts in the final product and its detection is essential to ensure that the Levothyroxine formulation is safe and effective for human use.
Chemically, Levothyroxine EP Impurity B is a derivative of L-tyrosine, an amino acid that is a precursor to the synthesis of thyroid hormones. It is also known as 3,5-Diiodo-L-tyrosine or DIT and has a molecular weight of 525.96 g/mol. The structure of Levothyroxine EP Impurity B contains two iodine atoms attached to the tyrosine molecule.
The presence of Levothyroxine EP Impurity B in the Levothyroxine formulation can affect the purity and potency of the medication, which can have adverse effects on patients. Therefore, it is important to monitor and control the levels of the impurity during the synthesis and manufacturing process of Levothyroxine.
In conclusion, Levothyroxine EP Impurity B plays a critical role in the quality control of Levothyroxine medication. Its chemical structure and properties make it a useful tool for monitoring the purity and potency of the final product, ensuring that patients receive safe and effective treatment for their thyroid hormone deficiency.
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Related Compounds
Levothyroxine Ethyl Ester | Levothyroxine EP Impurity H | Levothyroxine N- formamide Impurity | Levothyroxine- Impurity NMP | Levothyroxine Impurity 30 Sodium Salt | Levothyroxine - Impurity G | Levothyroxine Related Compound 10 | levothyroxine Dimer | Levothyroxine Lactose Adduct (O-lactoside) | TRIIODO-L-THYRONINE AMPOLA 100 µG/ML | Levothyroxine EP Impurity E | Levothyroxine EP Impurity I | Levothyroxine disodium salt | Levothyroxine Lactose Adduct (N-lactoside) | Levothyroxine Monochloro Impurity | Levothyroxine-4-Lactose Maillard Impurity | Levothyroxine EP Impurity C | Levothyroxine Glucose Adduct | O-(4-Hydroxy-3-iodophenyl) Levothyroxine | Levothyroxine- Impurity 5 | Levothyroxine EP Impurity K | Levothyroxine Sodium EP Impurity J | Levothyroxine Lactose Adduct |