Therapeutic Uses
Antihistamine
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
2-(2-(4-chlorophenyl)acetyl)benzoic acid
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
Azelastine EP Impurity C 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.
Azelastine EP Impurity C usage and description
Azelastine EP Impurity C is a chemical compound that is used as an impurity reference standard in the pharmaceutical industry. It is commonly used in the manufacturing of Azelastine hydrochloride, which is a type of antihistamine medication used to treat allergic rhinitis and other allergic conditions.
Chemically, Azelastine EP Impurity C is known as (E)-1-(2-((4-(4-chlorobenzyl)-2-(1H-tetrazol-5-yl)-1H-imidazol-1-yl)methyl)phenyl)-3-phenylprop-2-en-1-one. It is a white to off-white powder that is sparingly soluble in water but soluble in organic solvents such as methanol, ethanol, and DMSO.
As an impurity reference standard, Azelastine EP Impurity C is used to ensure the quality and purity of Azelastine hydrochloride. It is important to monitor impurities in pharmaceutical products as they can affect the safety and efficacy of the medication. Azelastine EP Impurity C is also used as a standard for analytical testing methods, such as high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS).
In conclusion, Azelastine EP Impurity C is a chemical compound that plays an important role in the quality control and manufacturing of Azelastine hydrochloride. Its usage as an impurity reference standard ensures that the medication is safe and effective for patients suffering from allergies.
