Escitalopram Oxalate BP-USP

Escitalopram Oxalate BP-USP Specification

Molecular Formula
C22H23FN2O5

Molecular Weight
414.43

Loss on Drying
1.0% w/w

Storage
Dry Place

Solubility
Freely soluble in methanol

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

CAS No
219861-08-2

Type
Pharmaceutical Intermediates

Grade
Industrial Grade

Usage
Pharmaceutical

Purity(%)
98.0 to 102.0%

Appearance
Fine to white slightly yellow powder

Physical Form
Powder

Escitalopram Oxalate BP-USP 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 Escitalopram Oxalate BP-USP

It is used to treat depression andgeneralized anxiety disorder (GAD). It is an antidepressant that belongs to agroup of medicines known as selective serotonin reuptake inhibitors (SSRIs).These medicines work by increasing the activity of the chemical serotonin inthe brain.

Exceptional Quality and Purity

Escitalopram Oxalate BP-USP guarantees consistent purity levels, ranging from 98.0% to 102.0%, making it suitable for rigorous pharmaceutical standards. Manufactured under strict guidelines, it comes as a fine to slightly yellowish powder, ensuring minimal impurities and reliable results during formulation.

Broad Pharmaceutical Applications

This compound is extensively utilized as an active intermediate in synthesizing antidepressant drugs. Its proven solubility in methanol and favorable handling characteristics support diverse industrial pharmaceutical processes, facilitating the production of high-efficacy medications around the world.

Safe Storage and Handling

To preserve its integrity, Escitalopram Oxalate BP-USP should be stored in a dry environment. Proper storage not only maintains its chemical stability but also extends its shelf life, keeping it ready for use in large-scale industrial and pharmaceutical manufacturing.

FAQs of Escitalopram Oxalate BP-USP:

Q: What is Escitalopram Oxalate BP-USP commonly used for?

A: Escitalopram Oxalate BP-USP is primarily used as a pharmaceutical intermediate in the manufacture of antidepressant medications. Its high purity and favorable chemical profile make it essential in pharmaceutical industries globally.

Q: How should Escitalopram Oxalate BP-USP be stored?

A: This compound should be stored in a dry place to ensure its chemical stability and to prevent degradation. Avoid exposure to moisture and direct sunlight for maximum shelf life.

Q: What are the key specifications of Escitalopram Oxalate BP-USP?

A: It features a purity of 98.0% to 102.0%, a molecular weight of 414.43, and a loss on drying of 1.0% w/w. The product appears as a fine to white slightly yellow powder and is freely soluble in methanol.

Q: When is Escitalopram Oxalate BP-USP introduced into the pharmaceutical production process?

A: It is typically used during the intermediate stages of synthesizing pharmaceuticals, particularly antidepressants, to ensure the final drug product meets regulatory requirements for quality and efficacy.

Q: Where is Escitalopram Oxalate BP-USP manufactured and exported from?

A: This pharmaceutical intermediate is manufactured and supplied in India and is available for export worldwide through reliable exporters, manufacturers, and suppliers.

Q: What benefits does Escitalopram Oxalate BP-USP offer to manufacturers?

A: Manufacturers benefit from its consistent high purity, optimal solubility in methanol, and stable physical form, which streamline the production process and contribute to high-quality end products.

Q: How does the loss on drying value affect the products usability?

A: The loss on drying value, capped at 1.0% w/w, ensures that the compound maintains low moisture content, which is crucial for maintaining its stability and suitability for pharmaceutical formulations.

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