Levothyroxine EP Impurity G hydrochloride
| Product Name | Levothyroxine EP Impurity G hydrochloride |
|---|---|
| CAT No. | CS-O-33624 |
| CAS No. | 2230724-39-5 (Freebase) |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 783.35 g/mol |
| Mol. For. | C₁₅H₁₄ClI₄NO₂ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| 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 G hydrochloride is a pharmaceutical impurity that is used in the development and testing of levothyroxine sodium drugs. Levothyroxine is a hormone that is naturally produced by the thyroid gland and is responsible for regulating metabolism and energy levels in the body. Levothyroxine sodium drugs are used to treat hypothyroidism, a condition where the thyroid gland does not produce enough of this hormone.
Levothyroxine EP Impurity G hydrochloride is a derivative of levothyroxine and is used as a reference standard in the development and testing of levothyroxine sodium drugs. It is also used as a quality control standard in the manufacture of these drugs to ensure their purity and potency.
The chemical formula of Levothyroxine EP Impurity G hydrochloride is C15H10I4NO4·HCl and its molecular weight is 799.46 g/mol. It is a white to off-white powder that is soluble in water and ethanol.
Levothyroxine EP Impurity G hydrochloride is classified as an organic compound and is a derivative of the amino acid tyrosine. It is a halogenated compound that contains four iodine atoms and a carboxylic acid group. Its chemical properties make it useful as a reference standard in the development and testing of levothyroxine sodium drugs.
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