Levothyroxine EP Impurity E
| Product Name | Levothyroxine EP Impurity E |
|---|---|
| Alternate Names | Levothyroxine Impurities, Impurities of Levothyroxine |
| CAT No. | CS-T-19369 |
| CAS No. | 1041-01-6 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 525.08 g/mol |
| Mol. For. | C₁₅H₁₃I₂NO₄ |
| 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(C[C@H](N)C(O)=O)=C1)OC2=CC=C(O)C=C2 |
| Canonical Smiles | C1=CC(=CC=C1O)OC2=C(C=C(C=C2I)CC(C(=O)O)N)I |
| InchIKey | ZHSOTLOTTDYIIK-ZDUSSCGKSA-N |
| Inchl | InChI=1S/C15H13I2NO4/c16-11-5-8(7-13(18)15(20)21)6-12(17)14(11)22-10-3-1-9(19)2-4-10/h1-6,13,19H,7,18H2,(H,20,21)/t13-/m0/s1 |
| IUPAC | (2S)-2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]propanoic 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 is a synthetic thyroid hormone that is widely used in the treatment of hypothyroidism. It is a potent medication that helps to regulate the levels of thyroid hormones in the body. However, as with any medication, there are impurities present in Levothyroxine that need to be taken into consideration.
One of the most important impurities in Levothyroxine is EP Impurity E. This impurity is also known as L-thyroxine-3,5-dinitrobenzoate and is a chemical compound that is formed during the manufacturing process of Levothyroxine. It is a yellow to orange crystalline powder that is insoluble in water and most organic solvents.
EP Impurity E is present in very small quantities in Levothyroxine, typically less than 0.1%. However, even at these low levels, it can have an impact on the efficacy and safety of the medication. Therefore, it is important to monitor the levels of this impurity in Levothyroxine and ensure that they are within acceptable limits.
In terms of usage, EP Impurity E is not used directly as a medication. Rather, it is a byproduct of the manufacturing process of Levothyroxine. However, it is important to consider its presence when prescribing and administering Levothyroxine to patients. Overall, EP Impurity E is an important consideration in the quality control of Levothyroxine and ensuring its safety and effectiveness in treating hypothyroidism.
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Related Compounds
Levothyroxine- Impurity 5 | levothyroxine Dimer | TRIIODO-L-THYRONINE AMPOLA 100 µG/ML | Levothyroxine-4-Lactose Maillard Impurity | Levothyroxine Related Compound 10 | O-(4-Hydroxy-3-iodophenyl) Levothyroxine | Levothyroxine Lactose Adduct (N-lactoside) | Levothyroxine Ethyl Ester | Levothyroxine disodium salt | Levothyroxine EP Impurity K | Levothyroxine- Impurity NMP | Levothyroxine - Impurity G | Levothyroxine Lactose Adduct (O-lactoside) | Levothyroxine Lactose Adduct | Levothyroxine EP Impurity H | Levothyroxine EP Impurity C | Levothyroxine Sodium EP Impurity J | Levothyroxine Monochloro Impurity | Levothyroxine Glucose Adduct | Levothyroxine N- formamide Impurity | Levothyroxine Impurity 30 Sodium Salt | Levothyroxine EP Impurity I | Levothyroxine EP Impurity B |