Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Levothyroxine T6 impurity(USP)
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Levothyroxine EP Impurity F is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
We are committed to offering products of the highest quality in order to meet the needs of our customers, and have elaborate systems in
place to ensure that material specifications, their certification and all handling and storage conditions are communicated at the time of
material handover.
We have invested in the highest quality packaging materials and use international logistics partners to service our customers. While all
possible precautions have been taken to deliver the required product(s), there may be some rare situations when our product does not
meet your requirements. Should that arise, please contact us with your concerns and we will endeavour to address them on a priority
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If there is an issue with one or more of our products, our policy is that it must be reported to us within 45 days of your receiving shipment.
While we will always address product issues after the 45 day return window has passed, we cannot issue a refund or account credit. As
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Levothyroxine EP Impurity F usage and description
Levothyroxine EP Impurity F is a chemical compound that is used in the production of levothyroxine, a medication that is used to treat hypothyroidism. Levothyroxine is a synthetic version of the thyroid hormone thyroxine, which is produced naturally by the thyroid gland. Hypothyroidism is a condition in which the thyroid gland does not produce enough thyroxine, resulting in symptoms such as fatigue, weight gain, and depression.
Levothyroxine EP Impurity F is a byproduct of the synthesis of levothyroxine. It is classified as an impurity because it is not the desired end product, but it is present in small quantities in the final product. The chemical formula of Levothyroxine EP Impurity F is C15H11I4NO4, and its molecular weight is 776.97 g/mol.
Levothyroxine EP Impurity F is typically removed from the final product through various purification methods, including chromatography and crystallization. The presence of impurities in pharmaceuticals is closely monitored by regulatory bodies such as the European Pharmacopoeia (EP), which sets standards for the purity and quality of medicines.
In conclusion, Levothyroxine EP Impurity F is a chemical compound that plays a crucial role in the production of levothyroxine, a medication used to treat hypothyroidism. Although it is present in small quantities in the final product, its removal is essential to ensure the purity and quality of the medication.
