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Arformoterol
References
FAQ's
References
- Murase, Kiyoshi; Mase, Toshiyasu; Ida, Hisashi; Takahashi, Kozo; Murakami, Masuo, Absolute configurations of four isomers of 3-formamido-4-hydroxy-α-[[N-(p-methoxy-α-methylphenethyl)amino]methyl]benzyl alcohol, a potent β-adrenoreceptor stimulant, Chemical & Pharmaceutical Bulletin, Volume: 26, Issue: 4, Pages: 1123-9, 1978
- Trofast, Jan; Oesterberg, Kristina; Kaellstroem, Britt Louise; Waldeck, Bertil, Steric aspects of agonism and antagonism at β-adrenoceptors: synthesis and pharmacological experiments with the enantiomers of formoterol and their diastereomers, Chirality, Volume: 3, Issue: 6, Pages: 443-50, 1991
- Butter, J. J.; van den Berg, B. T. J.; Portier, E. J. G.; Kaiser, G.; van Boxtel, C. J., Determination by HPLC with electrochemical detection of formoterol RR and SS enantiomers in urine, Journal of Liquid Chromatography & Related Technologies, Volume: 19, Issue: 6, Pages: 993-1005, 1996
Frequently Asked Questions
How are degradation impurities formed in Arformoterol?
Arformoterol can undergo various degradation pathways that lead to the formation of degradation impurities. These pathways include oxidation, deamination, and hydrolysis.
How can Arformoterol impurities be detected?
Arformoterol impurities are detected through various analytical methods such as High-Performance Liquid Chromatography (HPLC), liquid chromatography-mass spectrometry (LC-MS), etc.
Which solvent help in the analysis of Arformoterol impurities?
Methanol is a solvent used in analyzing Arformoterol impurities.
What are the temperature conditions required to store Arformoterol impurities?
Arformoterol impurities are stored at a controlled room temperature between 2-8 ⁰C or as indicated on the Certificate of Analysis (CoA).
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