Citalopram Hydrobromide -BP-USP-EP

Citalopram Hydrobromide -BP-USP-EP Specification

Molecular Weight
405.35

Molecular Formula
C20H21FN2O.HBr

HS Code
29420090

Solubility
Clear, colourless solution

Medicine Name
Citalopram

Chemical Name
()-1-(3-dimethylaminopropyl)-1-(4-fluorophenyl)-1, 3- dihydroisobenzofuran -5carbonitrile, HBR

CAS No
59729-32-7

Type
Pharmaceutical Intermediates

Grade
Industrial Grade

Usage
Pharmaceutical

Purity(%)
99%

Appearance
white to off-white powder

Physical Form
Powder

Citalopram Hydrobromide -BP-USP-EP Trade Information

Minimum Order Quantity
25 Kilograms

Main Export Market(s)
Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa

About Citalopram Hydrobromide -BP-USP-EP

Citalopram is used to treatdepression, including major depressive disorder (MDD). It is an antidepressantthat belongs to a group of medicines known as selective serotonin reuptakeinhibitors (SSRIs). These medicines are thought to work by increasing the activityof a chemical called serotonin in the brain.

Superior Chemical Purity for Pharmaceutical Applications

Our Citalopram Hydrobromide is synthesized to a high purity of 99%, ensuring reliability and effectiveness in pharmaceutical intermediates. This guarantees minimal impurities and consistency for manufacturers utilizing it in antidepressant drug formulations. The powders solubility profile allows seamless integration into various production processes, supporting a clear and colorless solution suitable for quality pharmaceutical outcomes.

Versatile Usage and Global Supply

Citalopram Hydrobromide, with HS Code 29420090 and CAS No. 59729-32-7, is tailored for industrial-scale pharmaceutical production. Our product adheres strictly to BP, USP, and EP guidelines, making it suitable for export and supply worldwide from India. Its consistent physical form (white to off-white powder) and robust molecular stability make it an optimal choice for pharmaceutical manufacturers and researchers.

FAQs of Citalopram Hydrobromide -BP-USP-EP:

Q: How is Citalopram Hydrobromide typically used in the pharmaceutical industry?

A: Citalopram Hydrobromide serves as a crucial intermediate in the synthesis of antidepressant medications, particularly formulations containing Citalopram. Its stability and high purity ensure optimal effectiveness in finished pharmaceutical products.

Q: What benefits does pharmaceutical-grade Citalopram Hydrobromide offer manufacturers?

A: With a purity of 99%, our pharmaceutical-grade product minimizes impurity risks, ensuring safe and effective end formulations. Its solubility in water adds versatility during manufacturing, while BP, USP, and EP compliance provides regulatory assurance.

Q: When should Citalopram Hydrobromide be selected over other intermediates?

A: Citalopram Hydrobromide is ideal when formulation purity, precise solubility, and compliance with international standards such as BP, USP, and EP are prerequisites for antidepressant production.

Q: Where is your Citalopram Hydrobromide manufactured and supplied?

A: Our Citalopram Hydrobromide is manufactured in India under stringent quality controls and supplied both domestically and to international markets through our established exporter network.

Q: What is the process of ensuring the quality and purity of your Citalopram Hydrobromide?

A: Quality assurance is maintained via adherence to BP-USP-EP protocols, rigorous purification, and analytical verifications. Each batch is tested for chemical consistency, solubility, and appearance before dispatch.

Q: How is Citalopram Hydrobromide supplied in terms of physical form and packaging?

A: The product is delivered as a white to off-white powder, tailored for industrial pharmaceutical processes. Packaging is designed to preserve purity and protect from moisture or contaminants during transit.

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