Fexofenadine Hydrochloride BP-USP

Fexofenadine Hydrochloride BP-USP Specification

Molecular Weight
538.12

Molecular Formula
C32H40ClNO4

Storage
Dry Place

Loss on Drying
2.0%

Solubility
Freely soluble in methanol slightly soluble in water very slightly soluble in acetone.

Shelf Life
5

Medicine Name
Fexofenadine

Chemical Name
Terfenadine carboxylate hydrochloride

CAS No
153439-40-8

Type
Pharmaceutical Intermediates

Grade
Industrial Grade

Usage
Pharmaceuticals

Purity(%)
99%

Appearance
White or almost white powder.

Physical Form
Powder

Fexofenadine Hydrochloride 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 Fexofenadine Hydrochloride BP-USP

Fexofenadine is an antihistamine. It is used to relieve the symptoms of hay fever (seasonal allergic rhinitis) and hives of the skin (chronic idiopathic urticaria) .Antihistamines work by preventing the effects of a substance called histamine, which is produced by the body. Histamine can cause itching, sneezing, runny nose, and watery eyes. Also, in some people histamine can close up the bronchial tubes (air passages of the lungs) and make breathing difficult. Histamine can also cause some people to have hives, with severe itching of the skin.

Premium Quality and Purity

Our Fexofenadine Hydrochloride BP-USP is produced under rigorous quality standards, achieving a purity of 99%. The physical form is a fine powder with strict controls on moisture content, ensuring a maximum loss on drying of 2.0%. This guarantees consistent results for pharmaceutical manufacturing processes.

Versatile Pharmaceutical Intermediate

Widely used as a key intermediate in the pharmaceutical industry, Fexofenadine Hydrochloride serves as the backbone for developing antihistamine medications to treat allergy symptoms. Its robust chemical profile enables efficient synthesis of finished dosage forms.

Safe Storage and Long Shelf Life

The compound should be stored in a dry place to maintain its stability and pharmacological effectiveness. With a shelf life of five years, it offers longevity and reduced risk of product degradation, ensuring reliable supply and stock management for manufacturers.

FAQs of Fexofenadine Hydrochloride BP-USP:

Q: How should Fexofenadine Hydrochloride BP-USP be stored to ensure stability?

A: Fexofenadine Hydrochloride BP-USP must be stored in a dry environment to protect it from moisture, which can affect its quality and purity. Proper storage extends its shelf life and maintains its effectiveness for pharmaceutical production.

Q: What is the primary usage of Fexofenadine Hydrochloride BP-USP in the pharmaceutical industry?

A: This compound is used as an intermediate in the synthesis of antihistamine drugs, particularly for producing Fexofenadine-based medications that treat allergy symptoms such as sneezing, runny nose, and itching.

Q: When should manufacturers use Fexofenadine Hydrochloride BP-USP in their process?

A: Manufacturers incorporate this intermediate during the early stages of drug synthesis, ensuring thorough integration and conversion into the final pharmaceutical product according to industry standards.

Q: Where is Fexofenadine Hydrochloride BP-USP commonly manufactured and exported?

A: Fexofenadine Hydrochloride BP-USP is produced, exported, and supplied primarily from India, taking advantage of the countrys advanced pharmaceutical manufacturing infrastructure and quality control protocols.

Q: What is the solubility profile of Fexofenadine Hydrochloride BP-USP?

A: Fexofenadine Hydrochloride BP-USP is freely soluble in methanol, slightly soluble in water, and very slightly soluble in acetone. This property is important for choosing appropriate solvents and processing conditions during pharmaceutical production.

Q: What benefits does Fexofenadine Hydrochloride BP-USP provide to drug manufacturers?

A: Its high purity, stable shelf life, and well-defined chemical characteristics make it ideal for reliable, large-scale pharmaceutical synthesis. These features help manufacturers maintain quality and regulatory compliance.

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