Storage Condition
Store at refrigerator (2-8°C) for long term storage
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 90%
Hazard Compound
No -Refer MSDS for accurate information
Levothyroxine Monochloro Impurity 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
basis. If there is no other option, we will either replace your product(s) or issue a refund or account credit, whichever you prefer.
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
always, we appreciate your support.
Levothyroxine Monochloro Impurity usage and description
Levothyroxine Monochloro Impurity is a chemical compound that is commonly used in the pharmaceutical industry. It is a synthetic derivative of the hormone thyroxine, which is produced by the thyroid gland in the human body. Levothyroxine Monochloro Impurity is used as an impurity standard in the quality control of Levothyroxine Sodium tablets.
Levothyroxine Monochloro Impurity is classified as a halide compound, which means it contains a halogen atom (in this case, chlorine) bound to a carbon atom. The chemical formula of Levothyroxine Monochloro Impurity is C15H10ClNO4, and its molecular weight is 313.7 g/mol.
The presence of Levothyroxine Monochloro Impurity in Levothyroxine Sodium tablets is closely monitored, as it can affect the quality and efficacy of the medication. Too much or too little Levothyroxine Monochloro Impurity can lead to adverse effects in patients, such as hypothyroidism or hyperthyroidism.
In conclusion, Levothyroxine Monochloro Impurity is a crucial chemical in the pharmaceutical industry. Its usage as an impurity standard ensures that Levothyroxine Sodium tablets are of high quality and safe for patient consumption. The careful monitoring of Levothyroxine Monochloro Impurity levels is essential to ensure the efficacy of the medication and prevent adverse effects in patients.
