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Formoterol

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Formoterol EP impurity D (Mixture of Diastereomers)

  • CAT Number DCTI-C-1029
  • CAS Number NA
  • Molecular Formula C20H26N2O4
  • Molecular Weight 358.43
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Formoterol-DCTI-C-1223-Daicel
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Formoterol EP Impurity-G

  • CAT Number DCTI-C-1223
  • CAS Number 64-13-1
  • Molecular Formula C10H15NO
  • Molecular Weight 165.24
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Formoterol-DCTI-C-1217-Daicel
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Formoterol impurity 3

  • CAT Number DCTI-C-1217
  • CAS Number NA
  • Molecular Formula C19H24N2O3
  • Molecular Weight 328.41
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Formoterol-DCTI-C-1117-Daicel
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Formoterol impurity-1

  • CAT Number DCTI-C-1117
  • CAS Number NA
  • Molecular Formula C20H26N2O4
  • Molecular Weight 358.44
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Formoterol-DCTI-C-1118-Daicel
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Formoterol impurity-2

  • CAT Number DCTI-C-1118
  • CAS Number NA
  • Molecular Formula C9H11NO3
  • Molecular Weight 181.19
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Formoterol Nitroso Impurity

  • CAT NUMBER DCTI-C-3651
  • CAS NUMBER NA
  • MOLECULAR FORMULA C19H23N3O5
  • MOLECULAR WEIGHT 373.41
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Formoterol-DCTI-C-1057-Daicel
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Formoterol related compound E (Mixture of Diastereomers)

  • CAT Number DCTI-C-1057
  • CAS Number 1616967-26-0
  • Molecular Formula C20H26N2O4
  • Molecular Weight 358.44
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Formoterol-DCTI-C-530-Daicel
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Formoterol related compound I

  • CAT Number DCTI-C-530
  • CAS Number 532414-36-1
  • Molecular Formula C19H24N2O4
  • Molecular Weight 344.41
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Formoterol-DCTI-C-1058-Daicel
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N-(2-(benzyloxy)-5-(1-hydroxyethyl)phenyl)formamide

  • CAT Number DCTI-C-1058
  • CAS Number NA
  • Molecular Formula C16H17NO3
  • Molecular Weight 271.32
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References
FAQ's

References

  1.  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
  1. Kamimura, Hidetaka; Sasaki, Hirokazu; Higuchi, Saburo; Shiobara, Yuichi, Quantitative determination of the β-adrenoceptor stimulant formoterol in urine by gas chromatography mass spectrometry, Journal of Chromatography, Biomedical Applications, Volume: 229, Issue: 2, Pages: 337-45, 1982

Frequently Asked Questions

The purpose of synthesizing Formoterol impurities is to identify, characterize, and quantify the impurities present in Formoterol drug products. It assesses Formoterol's safety, efficacy, and quality while ensuring compliance with regulatory guidelines.

Formoterol impurities are typically detected and quantified using analytical methods such as high-performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometry (LC-MS).

The polar solvent methanol helps in analyzing Formoterol and its impurities.

Formoterol impurities should be stored at a controlled room temperature between 2-8 ⁰C or as indicated on the Certificate of Analysis (CoA).

Note: Products protected by valid patents by a manufacturer are not offered for sale in countries having patent protection. The sale of such products constitutes a patent infringement, and its liability is at the buyer's risk.

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