Therapeutic Uses
Anti-Asthma / COPD
Storage Condition
Keep in a tightly closed vial, store in refrigerator
Synonyms
Bromhexine EP Impurity A
Application Notes
Useful research chemical for a range of applications
Hazard Compound
Yes -Refer MSDS for accurate information
Ambroxol EP Impurity A 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.
Ambroxol EP Impurity A usage and description
Ambroxol EP Impurity A is a pharmaceutical impurity that is used in the manufacturing of Ambroxol hydrochloride, which is commonly used as an expectorant in the treatment of respiratory disorders. The impurity is a byproduct of the synthesis of Ambroxol hydrochloride and is present in trace amounts in the final product.
Chemically, Ambroxol EP Impurity A is known as (2-amino-3,5-dibromo)benzoic acid, and its molecular formula is C7H5Br2NO2. It is a white or off-white crystalline powder that is sparingly soluble in water and ethanol. The impurity is known to be stable under normal storage conditions and does not pose any significant safety or health hazards.
The presence of Ambroxol EP Impurity A in Ambroxol hydrochloride is closely monitored, and it is subject to strict quality control measures to ensure that the impurity does not exceed the permissible limits set by regulatory authorities. The impurity is considered to be a degradation product of Ambroxol hydrochloride and is formed as a result of the hydrolysis of the amide bond in the molecule.
In conclusion, Ambroxol EP Impurity A is an important impurity in the manufacturing of Ambroxol hydrochloride, and its presence is closely monitored to ensure product quality and safety.
