Salbutamol EP Impurity F (Formate Salt)
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Salbutamol EP Impurity F (Formate Salt)

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Catalogue No.:VE009682
CAS No.:N/A
Mol. Formula:C27H42N2O7
Mol. Weight:506.63 g/mol

Additional information on Salbutamol EP Impurity F (Formate Salt)

Parent drug

Salbutamol

IUPAC Name

2,2′-(oxybis(methylene))bis(4-(2-(tert-butylamino)-1-hydroxyethyl)phenol) formate

Pharmacopoeial Synonyms

Albuterol Related Compound E / Salbutamol BP Impurity F

Other Synonyms

Salbutamol Dimer Ether

Smile

OC1=C(COCC2=C(O)C=CC(C(O)CNC(C)(C)C)C2)CC(C(O)CNC(C)(C)C)C=C1.[H]C(O)=O

InChI

InChI=1S/C27H40N2O6/c1-26(2,3)28-13-23(32)18-7-9-22(31)20(11-18)15-34-16-21-12-19(8-10-25(21)35-17-30)24(33)14-29-27(4,5)6/h7-12,17,23-24,28-29,31-33H,13-16H2,1-6H3

Description

Salbutamol EP Impurity F , also known in pharmacopoeias as Albuterol Related Compound E / Salbutamol BP Impurity F , is a highly characterized reference material. It fully complies with stringent regulatory standards, including those set by USP, EMA, JP, and BP. This product is essential for use in Abbreviated New Drug Applications (ANDA), New Drug Applications (NDA), and the commercial production of Salbutamol. Moreover, it comes with a detailed Structure Elucidation Report (SER), ensuring its accuracy and reliability for a wide range of analytical applications.

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