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Brexpiprazole - NDSRI's
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1-(benzo[b]thiophen-4-yl)-4-nitrosopiperazine

  • CAT NUMBER DCTI-C-004088
  • CAS NUMBER 2639426-95-0
  • MOLECULAR FORMULA C12H13N3OS
  • MOLECULAR WEIGHT 247.32
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7-(4-(4-nitrosopiperazin-1-yl)butoxy)quinolin-2(1H)-one 

  • CAT NUMBER DCTI-C-004120
  • CAS NUMBER NA
  • MOLECULAR FORMULA C17H22N4O3
  • MOLECULAR WEIGHT 330.39
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References
FAQ's

References

  1. Yamashita, Hiroshi; Matsubara, Jun; Oshima, Kunio; Kuroda, Hideaki; Ito, Nobuaki; Miyamura, Shin; Shimizu, Satoshi; Tanaka, Tatsuyoshi; Oshiro, Yasuo; Shimada, Jun; et al, Piperazine-Substituted Benzothiophenes For Treatment Of Mental Disorders, Otsuka Pharmaceutical Co., Ltd., Japan, EP1869025B1, January 26, 2011
  2. Bhawar, H. S.; Sanket, Thete; Shinde, G. S., Development and validation of stability indicating RP-HPLC method for estimation of Brexpiprazole from bulk and tablet form, Journal of Drug Delivery and Therapeutics, Volume: 9, Issue: 4, Pages: 141-145, 2019

Frequently Asked Questions

The methods for controlling Brexpiprazole impurities include optimizing the synthetic process, using high-quality raw materials, employing effective purification methods, and implementing analytical methods to detect and quantify impurities.

The presence of impurities in Brexpiprazole can reduce its shelf life and stability, leading to a shorter expiration date.

Impurities in Brexpiprazole are typically detected using analytical techniques such as high-performance liquid chromatography (HPLC) or liquid chromatography-mass spectrometry (LC-MS).

Brexpiprazole 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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