Ambroxol EP Impurity A

Product Name Ambroxol EP Impurity A
Alternate Names Ambroxol Impurities, Impurities of Ambroxol
CAT No. CS-O-07152
CAS No. 50739-76-9
Category Impurities
Stock IN-Stock
Mol. Wt. 280.94 g/mol
Mol. For. C₇H₇Br₂NO
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Ambroxol
Purity >98%
Therapeutic Anti-Asthma / COPD
Smileys OCC(C=C(Br)C=C1Br)=C1N
Canonical Smiles C1=C(C=C(C(=C1CO)N)Br)Br
InchIKey GHUMSGGCKVMYGH-UHFFFAOYSA-N
Inchl InChI=1S/C7H7Br2NO/c8-5-1-4(3-11)7(10)6(9)2-5/h1-2,11H,3,10H2
IUPAC (2-amino-3,5-dibromophenyl)methanol
Controlled No
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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.

Related Compounds

Ambroxol EP Impurity E | Ambroxol hydrochloride EP Impurity B | N-Nitroso-Ambroxol | Ambroxol EP Impurity D | Ambroxol Monobromine HCl salt |

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