Therapeutic Uses
Anti-Hypertensives
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Perindopril EP Impurity I, 145513-33-3
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Perindopril EP Impurity I 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
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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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Perindopril EP Impurity I usage and description
Perindopril EP Impurity I is a pharmaceutical impurity that is commonly used in the production of antihypertensive drugs such as Perindopril. The impurity is added during the synthesis process of Perindopril to enhance its therapeutic effects. The chemical name of Perindopril EP Impurity I is (2S,3aS,7aS)-1-[(2S)-2-[[(2S)-2-[(1S)-1-carboxybutyl]amino]propanoyl]amino]octahydro-1H-indole-2-carboxylic acid.
Perindopril EP Impurity I is a chiral compound, which means that it exists in two mirror-image forms known as enantiomers. These enantiomers have different biological activities, and the production of Perindopril involves the separation of the enantiomers to produce the desired therapeutic effect.
The usage and chemical information of Perindopril EP Impurity I are critical to the quality control and regulatory compliance of Perindopril-based drugs. The impurity is closely monitored during the production process to ensure that it meets the strict quality standards required by the pharmaceutical industry. The chemical properties of Perindopril EP Impurity I are also important in determining its stability, solubility, and bioavailability, which affect its therapeutic efficacy and safety.
In conclusion, Perindopril EP Impurity I is an essential component in the production of Perindopril-based antihypertensive drugs. Its usage and chemical information play a crucial role in ensuring the quality and safety of these drugs, making it a vital component of the pharmaceutical industry.
