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Carvedilol

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Carvedilol EP Impurity- A.TFA salt

  • CAT NUMBER DCTI-C-2354
  • CAS NUMBER 1198090-73-1 (Free Base)
  • MOLECULAR FORMULA C36H43N3O7 (Free base); C38H44F3N3O9 (Salt)
  • MOLECULAR WEIGHT 629.75 (Free base); 743.78 (Salt)
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Carvedilol EP Impurity-C

  • CAT NUMBER DCTI-C-2356
  • CAS NUMBER 72955-94-3
  • MOLECULAR FORMULA C31H32N2O4
  • MOLECULAR WEIGHT 496.61
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Carvedilol Impurity 12

  • CAT NUMBER DCTI-C-2275
  • CAS NUMBER 1059573-45-3
  • MOLECULAR FORMULA C33H36N2O6
  • MOLECULAR WEIGHT 556.66
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Carvedilol Impurity Bis Stage-A amine coupling

  • CAT NUMBER DCTI-C-2357
  • CAS NUMBER NA
  • MOLECULAR FORMULA C34H38N4O5
  • MOLECULAR WEIGHT 582.7
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Carvedilol Labelled Standard

  • CAT Number DCTI-A-105
  • CAS Number 1133705-56-2
  • Molecular Formula C24H22D4N2O4
  • Molecular Weight 410.51
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Carvedilol Nitroso Impurity

  • CAT NUMBER DCTI-C-3052
  • CAS NUMBER NA
  • MOLECULAR FORMULA C24H25N3O5
  • MOLECULAR WEIGHT 435.48
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Carvedilol Related Compound D

  • CAT NUMBER DCTI-C-2358
  • CAS NUMBER 51997-51-4
  • MOLECULAR FORMULA C15H13NO2
  • MOLECULAR WEIGHT 239.27
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Carvedilol Related Compound F

  • CAT NUMBER DCTI-C-2305
  • CAS NUMBER 1246820-73-4
  • MOLECULAR FORMULA C24H30N2O4
  • MOLECULAR WEIGHT 410.51
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N-​Isopropyl Carvedilol

  • CAT NUMBER DCTI-C-2352
  • CAS NUMBER 1246819-01-1
  • MOLECULAR FORMULA C27H32N2O4
  • MOLECULAR WEIGHT 448.56
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References
FAQ's

References

  1. Wiedemann, Fritz; Kampe, Wolfgang; Thiel, Max; Sponer, Gisbert; Roesch, Egon; Dietmann, Karl, Derivatives Of Carbazolyl-4-Oxypropanolamine, Methods For Their Preparation And Medicines Containing Them, Boehringer Mannheim G.m.b.H., Federal Republic of Germany, EP4920B1, August 5, 1981
  2. Reiff, K., High-performance liquid chromatographic method for the determination of carvedilol and its demethyl metabolite in body fluids, Journal of Chromatography, Biomedical Applications, Volume: 413, Pages: 355-62, 1987

Frequently Asked Questions

Impurities in Carvedilol are identified using analytical techniques such as high-performance liquid chromatography (HPLC), liquid chromatography (LC), mass spectrometry (MS), etc.

The limits for impurities in Carvedilol set by regulatory agencies are  ≤0.2% for individuals and ≤0.5% for total impurities.

Impurity standards in Carvedilol help identify and quantify impurities in the drug substance. They are also used to develop and validate analytical methods for impurity identification and quantification.

Carvedilol impurities are stored at a controlled room temperature between 2-8 °C 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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