Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
3-(3,4-Dihydroxyphenyl)-D-alanine;D-3-Hydroxytyrosine, D-DOPA
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Levodopa EP Impurity D 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.
Levodopa EP Impurity D usage and description
Levodopa EP impurity D is a chemical compound that is used as an analytical standard and reference material in the pharmaceutical industry. It is a derivative of Levodopa, which is a medication used to treat Parkinson's disease. Levodopa EP impurity D is one of the many impurities that can be found in Levodopa, and its presence can affect the purity and quality of the medication.
Chemically, Levodopa EP impurity D is known as 3,4-Dihydroxyphenylacetaldehyde. It is a yellow to brownish-yellow crystalline powder that is soluble in water and ethanol. Its molecular formula is C8H8O3 and its molecular weight is 152.15 g/mol.
Levodopa EP impurity D is used in the analysis and identification of impurities in Levodopa. It is also used in research and development of new drugs that target the same neurological pathways as Levodopa. The presence of impurities in pharmaceuticals can affect the efficacy and safety of the medication, which is why Levodopa EP impurity D is an important tool in the quality control process.
In conclusion, Levodopa EP impurity D is a useful reference material for the pharmaceutical industry. Its chemical properties and usage make it a valuable tool for ensuring the purity and quality of Levodopa and other medications that target the same neurological pathways.
