Levothyroxine EP Impurity C
| Product Name | Levothyroxine EP Impurity C |
|---|---|
| Alternate Names | Levothyroxine Impurities, Impurities of Levothyroxine |
| CAT No. | CS-T-45488 |
| CAS No. | 51-24-1 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 621.93 g/mol |
| Mol. For. | C₁₄H₉I₃O₄ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Levothyroxine |
| Purity | 95% |
| Smileys | IC1=C(C(I)=CC(CC(O)=O)=C1)OC2=CC(I)=C(O)C=C2 |
| Canonical Smiles | C1=CC(=C(C=C1OC2=C(C=C(C=C2I)CC(=O)O)I)I)O |
| InchIKey | UOWZUVNAGUAEQC-UHFFFAOYSA-N |
| Inchl | InChI=1S/C14H9I3O4/c15-9-6-8(1-2-12(9)18)21-14-10(16)3-7(4-11(14)17)5-13(19)20/h1-4,6,18H,5H2,(H,19,20) |
| IUPAC | 2-[4-(4-hydroxy-3-iodophenoxy)-3,5-diiodophenyl]acetic acid |
| 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 C is a chemical compound that is used in the pharmaceutical industry as a reference standard for the analysis and quantification of impurities in Levothyroxine sodium, a medication used for the treatment of hypothyroidism. This impurity is also known as 3,5-diiodo-L-tyrosine.
Levothyroxine EP Impurity C is a derivative of the amino acid tyrosine and is structurally similar to Levothyroxine sodium. It is classified as an organic compound and has a molecular formula of C9H8I2NO4. The compound is a white to off-white crystalline powder and has a melting point of 220-225°C.
The chemical properties of Levothyroxine EP Impurity C make it an ideal reference standard for the analysis of impurities in Levothyroxine sodium. It is used in the pharmaceutical industry to ensure that the Levothyroxine sodium medication is of high quality and meets regulatory standards. The compound is also used in research and development to study the effects of impurities on the efficacy and safety of Levothyroxine sodium.
In conclusion, Levothyroxine EP Impurity C is an important reference standard in the pharmaceutical industry. Its chemical properties make it useful for the analysis and quantification of impurities in Levothyroxine sodium, ensuring that the medication is of high quality and meets regulatory standards.
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Related Compounds
Levothyroxine- Impurity 5 | Levothyroxine Glucose Adduct | Levothyroxine Lactose Adduct (N-lactoside) | Levothyroxine Lactose Adduct (O-lactoside) | Levothyroxine - Impurity G | Levothyroxine- Impurity NMP | Levothyroxine Related Compound 10 | Levothyroxine disodium salt | Levothyroxine Monochloro Impurity | Levothyroxine Ethyl Ester | Levothyroxine EP Impurity B | Levothyroxine EP Impurity K | TRIIODO-L-THYRONINE AMPOLA 100 µG/ML | Levothyroxine Impurity 30 Sodium Salt | Levothyroxine Sodium EP Impurity J | Levothyroxine EP Impurity E | levothyroxine Dimer | Levothyroxine Lactose Adduct | Levothyroxine EP Impurity I | Levothyroxine N- formamide Impurity | O-(4-Hydroxy-3-iodophenyl) Levothyroxine | Levothyroxine-4-Lactose Maillard Impurity | Levothyroxine EP Impurity H |