Formoterol
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Formoterol EP Impurity I
| SZ CAT No: | SZ-F005009 |
| CAS No | 532414-36-1 |
| Mol.F. | C19H24N2O4 |
| Mol.Wt. | 344.4 |
| Inv. Status | In Stock |
| Shipping Condition | Room Temperature |
Chemical Name: N-[2-Hydroxy-5-[(1RS)-1-hydroxy-2-[[(1SR)-2-(4-methoxyphenyl)-1-methylethyl]amino]ethyl]phenyl]formamide (as per EP);N-(2-hydroxy-5-[(RS)-1-hydroxy-2-{[(SR)-1-(4-methoxyphenyl)propan-2-yl]amino}ethyl]phenyl)formamide (as per USP)
Synonym: Formoterol USP Related Compound I ; rel-(R,S)-Formoterol ; anti-rac-Formoterol
Shipping Temperature: Room Temperature
HSN Code: 38229010
Country of Origin: India
Smiles: OC(C1=CC(NC=O)=C(O)C=C1)CNC(C)CC2=CC=C(OC)C=C2
Formoterol EP Impurity I is chemically N-[2-Hydroxy-5-[(1RS)-1-hydroxy-2-[[(1SR)-2-(4-methoxyphenyl)-1-methylethyl]amino]ethyl]phenyl]formamide (as per EP);N-(2-hydroxy-5-[(RS)-1-hydroxy-2-{[(SR)-1-(4-methoxyphenyl)propan-2-yl]amino}ethyl]phenyl)formamide (as per USP). It is also known as Formoterol USP Related Compound I ; rel-(R,S)-Formoterol ; anti-rac-Formoterol. Formoterol EP Impurity I is supplied with detailed characterization data compliant with regulatory guideline. Formoterol EP Impurity I can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Formoterol.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.
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