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Postion:Product Catalog >Analytical Chemistry>Standard>Pharmaceutical Impurity Reference Standards>Citalopram EP Impurity F
Citalopram EP Impurity F
  • Citalopram EP Impurity F
  • Citalopram EP Impurity F
  • Citalopram EP Impurity F
  • Citalopram EP Impurity F

Citalopram EP Impurity F NEW

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Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-07-31

Product Details

Product Name: Citalopram EP Impurity F CAS No.: 64169-39-7
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/31

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WhatsAPP: +86 17320513646
E-mail: anna@molcoo.com

Product Basic Information

  • Product Number: C037012

  • English Name: Citalopram EP Impurity F

  • English Alias: 3-(5 - bromo - 1 -(4 - fluorophenyl)-1,3 - dihydroisobenzofuran - 1 - yl)-N,N - dimethylpropan - 1 - amine; 1644389 - 68 - 3(HCl)

  • CAS Number: 64169 - 39 - 7

  • Molecular Formula: C19H21BrFNO

  • Molecular Weight: 378.28

Product Background

Citalopram is a widely used antidepressant in clinical practice, belonging to the class of selective serotonin reuptake inhibitors (SSRIs). During the synthesis, storage, or metabolism of citalopram, various impurities may be produced, and Citalopram EP Impurity F is one of the impurities of concern. The study of drug impurities is an important part of drug quality control, because the presence of impurities may affect the safety, effectiveness, and stability of drugs. Understanding and controlling these impurities are crucial to ensuring the quality of drugs and the safety of patients' medication.

Research Status

At present, the research on Citalopram EP Impurity F mainly focuses on the fields of drug analysis and quality control. Researchers are committed to developing highly sensitive and selective analytical methods to detect the content of this impurity in drugs, such as high - performance liquid chromatography (HPLC), gas chromatography - mass spectrometry (GC - MS), etc. Through these methods, the residual amount of Citalopram EP Impurity F in drug preparations can be accurately determined, so as to ensure that the drugs meet the quality standards. In addition, there are also studies focusing on the formation mechanism of this impurity, so as to take corresponding measures in the drug production process to reduce its formation and improve the purity and quality of drugs.


NOTE!

We can also customize related analogues and modified peptides including HPLC, MS, 1H-NMR, MS, HPLC, IR, UV, COA, MSDS.
This product is intended for laboratory use only!

WhatsAPP: +86 17320513646
E-mail: anna@molcoo.com


NEW IN STOCK!

The Molcoo Laboratory added drug impurity reference standards, including Baricitinib, Piperazine, Benzylpenicillin, Tranilast and multiple N-Nitroso drug impurities! Now available for immediate delivery! 










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