Citalopram Standard (CAS 59729-33-8) and Impurities: Key Elements in Pharmaceutical Testing

Citalopram, a selective serotonin reuptake inhibitor (SSRI), is increasingly affirming its indispensable role in the medical field. It is used to treat depression. Citalopram was discovered in 1977 and began to be used medically in 1998. To ensure the therapeutic efficacy and absolute safety of the drug, strict quality control through Citalopram standards (CAS 59729-33-8) and Citalopram impurities is extremely essential. This article will delve into the importance of Citalopram standards and impurities and introduce a solution for providing reputable standards that meet the most stringent standards of the pharmaceutical industry.

Detailed Information on Citalopram Standard

• Chemical Name: Citalopram
• CAS Number: 59729-33-8
• Molecular Formula: C20H21FN2O
• Molecular Weight: 324.39
• Synonyms: Nitalapram, Cipram
• Appearance: White to off-white solid
• Storage Conditions: 2-8°C (refrigerator)

Outstanding Importance of Citalopram Standards and Impurities

In the field of pharmaceutical production and testing, quality control is the key factor in ensuring the safety, efficacy, and legal compliance of the product. For Citalopram, the use of pharmaceutical standards and Citalopram impurities plays a crucial role in many aspects:

• Qualitative and Quantitative Analysis: Citalopram standard (CAS 59729-33-8) helps to accurately determine the amount of Citalopram in the final product, ensuring the correct dosage and therapeutic efficacy.
• Purity Control: Citalopram impurities help assess the presence and amount of impurities that may arise during synthesis or storage. Impurity control is mandatory to prevent unwanted substances from affecting the quality and safety of the drug.
• Research and Development (R&D): Standards and impurities support the process of active ingredient synthesis, formula optimization, and stability testing of Citalopram under various conditions.
• Ensuring Compliance with International Pharmacopoeias: The use of standards according to the pharmacopoeia is a mandatory requirement for pharmaceutical manufacturers to comply with the industry’s strict regulations, thereby ensuring that the product is allowed to be marketed globally.

Reliable Source of Citalopram Standards and Impurities

We are proud to be a reputable supplier of high-quality Citalopram standards (CAS 59729-33-8) and Citalopram impurities, fully meeting the stringent requirements of the pharmaceutical industry. Our product catalog includes Citalopram reference standards, and pharmacopoeial and non-pharmacopoeial impurities, as well as stable isotopes. Specifically:

• Citalopram standard
• Pharmacopoeial impurities of Citalopram: Including impurities listed and controlled according to international pharmacopoeias.
• Non-pharmacopoeial impurities of Citalopram: Other impurities that may arise but are not officially listed in the pharmacopoeia, still need to be controlled to ensure product safety.
• Stable isotopes of Citalopram: Isotopic versions of Citalopram used in in-depth research, mass spectrometry analysis, and bioavailability testing.

Benefits of choosing our products:

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• Optimal storage and transportation: Products are stored under ideal conditions (2-8°C) and shipped under standard conditions to maintain the best quality from warehouse to customer.

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Investing in high-quality Citalopram standards (CAS 59729-33-8) and Citalopram impurities is not only a mandatory requirement but also a key factor in ensuring the safety and efficacy of pharmaceutical products. Let us be your trusted partner in your quality control journey.

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