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Clopidogrel Bisulfate BP-USP

Clopidogrel Bisulfate BP-USP
Clopidogrel Bisulfate BP-USP

Clopidogrel Bisulfate BP-USP Specification

  • Storage
  • Dry Place
  • Molecular Formula
  • C16H16ClNO2SH2SO4
  • Solubility
  • Freely soluble at pH1 and practically insoluble in neutral pH.
  • Molecular Weight
  • 321.82 g/mol
  • Shelf Life
  • 4 Years
  • Loss on Drying
  • 0.5%
  • Medicine Name
  • Clopidogrel
  • Chemical Name
  • (+)-(S)-methyl 2-(2-chlorophenyl)-2-(6, 7-dihydrothieno [3, 2-c] pyridin-5(4H)-yl) acetate
  • CAS No
  • 113665-84-2
  • Type
  • Pharmaceutical Intermediates
  • Grade
  • Industrial Grade
  • Usage
  • Pharmaceutical
  • Purity(%)
  • 97.0%-101.5%
  • Appearance
  • White off white free flowing powder.
  • Physical Form
  • Powder
 

Clopidogrel Bisulfate BP-USP Trade Information

  • Minimum Order Quantity
  • 100 Kilograms
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
 

About Clopidogrel Bisulfate BP-USP

It is usedalone or together with aspirin to lessen the chance of a heart attack orstroke. It is given to patients with acute coronary syndrome (ACS), to patientswho have already had a heart attack, severe chest pain, or a stroke, or topatients with other circulation problems (eg, peripheral arterial disease) thatcould cause a stroke or heart attack. Acute coronary syndrome is a conditionwhere the blood flow to the heart is blocked.


Key Features and Quality Standards

Clopidogrel Bisulfate BP-USP adheres to both BP and USP standards, ensuring consistent quality for pharmaceutical use. Its industrial-grade nature allows for effective integration into large-scale manufacturing. With high purity and reliable chemical properties, it meets the stringent requirements of the pharmaceutical industry.


Applications and Benefits in Pharmaceuticals

Primarily used as a pharmaceutical intermediate, Clopidogrel Bisulfate facilitates the production of antiplatelet drugs. Thanks to its precise composition and stability, it enhances the efficiency of medication synthesis processes. Its white to off-white appearance and free-flowing nature simplify handling and measurement during formulation.


Storage, Stability, and Handling

To preserve its integrity and effectiveness, Clopidogrel Bisulfate BP-USP should be stored in a dry environment. Its low loss on drying (0.5%) and four-year shelf life ensure longevity and dependability, making it a cost-effective choice for manufacturers and suppliers.

FAQs of Clopidogrel Bisulfate BP-USP:


Q: How should Clopidogrel Bisulfate BP-USP be stored to maintain its quality?

A: Clopidogrel Bisulfate BP-USP should be kept in a dry place to prevent moisture absorption, which helps maintain its stability and prolongs its shelf life up to four years.

Q: What is the primary usage of Clopidogrel Bisulfate BP-USP powder?

A: This product serves as a pharmaceutical intermediate, mainly used in the synthesis of antiplatelet agents such as Clopidogrel, which helps prevent blood clots.

Q: When is Clopidogrel Bisulfate BP-USP typically used during the pharmaceutical manufacturing process?

A: Clopidogrel Bisulfate BP-USP is introduced during the intermediate stages of active pharmaceutical ingredient synthesis before formulating the final medication.

Q: Where does Clopidogrel Bisulfate BP-USP exhibit optimal solubility?

A: It is freely soluble in highly acidic environments (at pH 1) but remains practically insoluble at neutral pH, making it suitable for specific pharmaceutical formulations.

Q: What process ensures the consistent free-flowing appearance of Clopidogrel Bisulfate BP-USP?

A: Careful manufacturing and stringent drying protocols result in the powders white to off-white color and free-flowing texture, which simplifies handling during production.

Q: What are the main benefits of using Clopidogrel Bisulfate BP-USP for manufacturers?

A: Manufacturers benefit from its high purity, long shelf life, easy handling, and compliance with BP and USP standards, ensuring consistent and reliable pharmaceutical outputs.

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