Therapeutic Uses
Anti-Asthma / COPD
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Acetylsalicylic Acid EP Impurity D (Aspirin Impurity D); Acetylsalicylsalicylic Acid; 2-(Acetyloxy)benzoic Acid 2-Carboxyphenyl Ester; Acesalum; Diplosal Acetate; Diplosalacetat; Salicylacetylsalicylic Acid; Aspirin Impurity D
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
"Not less than 95%
"
Hazard Compound
No -Refer MSDS for accurate information
Aspirin 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.
Aspirin EP Impurity D usage and description
Aspirin EP Impurity D, also known as 2-Acetoxybenzoic acid, is a chemical compound that is commonly used as a reference standard in the pharmaceutical industry. This impurity is a byproduct of the synthesis of Aspirin, an analgesic and anti-inflammatory drug that is widely used to alleviate pain and reduce inflammation.
Aspirin EP Impurity D is a white crystalline powder that has a molecular weight of 180.16 g/mol. It is soluble in methanol, ethanol, and chloroform, and has a melting point of 146-149°C. The chemical formula of Aspirin EP Impurity D is C9H8O4.
This impurity is considered to be a significant impurity in Aspirin, and its presence in the final product can affect the quality and efficacy of the drug. Therefore, it is essential to monitor the levels of Aspirin EP Impurity D during the manufacturing process of Aspirin.
Aspirin EP Impurity D is also used as a reference standard in the development and validation of analytical methods for the detection and quantification of impurities in pharmaceuticals. It is an important tool for ensuring the safety, efficacy, and quality of pharmaceutical products.
In conclusion, Aspirin EP Impurity D is a crucial reference standard in the pharmaceutical industry, used to monitor and control the levels of impurities in Aspirin and other pharmaceutical products. Its accurate detection and quantification are essential for ensuring the safety and efficacy of these drugs.
