Quinine Dihydrochloride BP

Product Description

Quinine Dihydrochloride BP is a pharmaceutical-grade active pharmaceutical ingredient (API) primarily used for the treatment of malaria, muscle cramps, and fever reduction. It is a water-soluble salt of quinine, derived from the Cinchona bark, and is known for its antimalarial, analgesic, and muscle relaxant properties.

At Prism Industries Pvt. Ltd., we manufacture high-purity Quinine Dihydrochloride BP in strict compliance with British Pharmacopoeia (BP) standards. Our Quinine Dihydrochloride BP undergoes rigorous quality control, ensuring purity, potency, and compliance for pharmaceutical formulations.

Identification

  • Chemical Name: Quinine Dihydrochloride
  • Molecular Formula: C20H24N2O2·2HCl·2H2O
  • Molecular Weight: 397.34 g/mol
  • CAS Number: [Specific CAS Number]
  • Synonyms: Quinine 2HCl, Dihydrochloride of Quinine
  • Appearance: White to slightly yellow crystalline powder
  • Odor: Odorless or slightly bitter odor
  • Solubility: Highly soluble in water, sparingly soluble in alcohol
  • Function: Used as an antimalarial agent, muscle relaxant, and fever reducer

Quinine Dihydrochloride BP is widely used in pharmaceutical formulations for oral and injectable medications, offering rapid absorption and high bioavailability.

Quinine Dihydrochloride BP

Regulatory Documents & Compliance

At Prism Industries Pvt. Ltd., we ensure that Quinine Dihydrochloride BP meets global regulatory standards and provide the following regulatory documents:

  • Certificate of Analysis (COA): Confirms purity, potency, and compliance with BP standards.
  • Material Safety Data Sheet (MSDS): Provides safety, handling, and storage guidelines.
  • Good Manufacturing Practices (GMP) Certificate: Ensures production under strict pharmaceutical-grade quality control.
  • British Pharmacopoeia (BP) Compliance: Adheres to BP specifications for pharmaceutical use.
  • TSE/BSE-Free Statement: Confirms that the product is free from animal-derived materials.
  • Stability Data Report: Provides information on long-term stability under various conditions.
  • Residual Solvents Report: Ensures compliance with ICH Q3C guidelines for safe solvent levels.
  • Allergen-Free Statement: Certifies that the product is free from common allergens.

Our commitment to regulatory compliance ensures that Quinine Dihydrochloride BP meets the highest quality and safety standards for pharmaceutical formulations.

Specifications of Quinine Dihydrochloride BP

Our Quinine Dihydrochloride BP is manufactured under strict quality control conditions, meeting the following pharmaceutical specifications:

Parameter

Specification

Appearance

White to slightly yellow crystalline powder

Odor

Odorless or faintly bitter odor

Identification

Positive for Quinine Dihydrochloride

Melting Point

175°C – 190°C

Solubility

Freely soluble in water, sparingly soluble in alcohol

pH (5% Solution in Water)

4.5 – 6.5

Assay (Purity by HPLC)

98.0% – 102.0%

Loss on Drying

≤ 2.0%

Heavy Metals

≤ 10 ppm

Residual Solvents

Complies with ICH Q3C guidelines

Microbial Limits

Complies with BP standards

Our Quinine Dihydrochloride BP meets strict pharmaceutical standards, ensuring its purity, consistency, and safety for medical and research applications.

Solubility of Quinine Dihydrochloride BP

 

The solubility of Quinine Dihydrochloride BP is a key factor in its pharmaceutical applications.

  • Water: Freely soluble, making it ideal for oral and injectable formulations.
  • Alcohol: Sparingly soluble.
  • Acidic Solutions: Highly soluble, ensuring rapid absorption in the body.
  • Organic Solvents: Partially soluble in some organic solvents like ether.

Due to its high water solubility, Quinine Dihydrochloride BP is widely used in intravenous and oral dosage forms for rapid therapeutic action.

Assay of Quinine Dihydrochloride BP

 

The assay of Quinine Dihydrochloride BP is performed using High-Performance Liquid Chromatography (HPLC) to ensure purity and potency.

HPLC Assay Method for Quinine Dihydrochloride BP

 

  • Instrument: High-Performance Liquid Chromatography (HPLC)
  • Mobile Phase: Acetonitrile: Water (60:40) with 0.1% phosphoric acid
  • Column: C18 (250 mm × 4.6 mm, 5 µm)
  • Flow Rate: 1.0 mL/min
  • Detection Wavelength: 254 nm
  • Injection Volume: 10 µL
  • Retention Time: 5.5 ± 0.3 minutes
  • Assay Specification: 98.0% – 102.0%

Our Quinine Dihydrochloride BP undergoes HPLC analysis to ensure it meets assay specifications, providing high purity and accurate dosage for pharmaceutical applications.

Chromatographic Purity by HPLC

The chromatographic purity of Quinine Dihydrochloride BP is determined to identify and quantify impurities using HPLC methods.

HPLC Conditions for Chromatographic Purity Analysis

  • Mobile Phase: Acetonitrile: Phosphate Buffer (70:30)
  • Column: C18 (150 mm × 4.6 mm, 5 µm)
  • Flow Rate: 1.2 mL/min
  • Detection Wavelength: 260 nm
  • Retention Time: 5.0 ± 0.3 minutes
  • Total Impurities Limit: ≤ 0.5%

Our Quinine Dihydrochloride BP undergoes rigorous HPLC testing to ensure pharmaceutical-grade purity and efficacy.

Why Choose Prism Industries Pvt. Ltd. for Quinine Dihydrochloride BP?

As a leading manufacturer of Quinine Dihydrochloride BP, Prism Industries Pvt. Ltd. ensures:

Pharmaceutical-Grade Purity: Meets BP, GMP, and global pharmacopeial standards.
High Solubility & Stability: Ensures fast absorption and effectiveness.
Advanced Quality Control: Rigorous HPLC and microbiological testing.
Global Regulatory Compliance: Ensures safety, purity, and compliance.
Reliable Supply Chain: Capable of bulk production and worldwide distribution.

Quinine Dihydrochloride BP is a highly effective antimalarial agent with excellent solubility, purity, and stability. At Prism Industries Pvt. Ltd., we ensure top-quality production, regulatory compliance, and superior quality control for Quinine Dihydrochloride BP, making it ideal for pharmaceutical applications.

For high-quality Quinine Dihydrochloride BP, contact us today for bulk supply and customized pharmaceutical solutions.

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Our minimum order quantities vary depending on the product:

  • Active Pharmaceutical Ingredients (APIs): 1 kg
  • Excipients: 5 kg
  • Finished Dosage Forms: 1,000 units
  • Custom Orders: Determined on a case-by-case basis

We accept the following payment methods:

  • Bank Transfers: EUR, USD, GBP
  • Credit/Debit Cards: Visa, MasterCard
  • PayPal: For international transactions

API Pharmaceutical Manufacturing Company is a dedicated manufacturer of high-quality pharmaceutical ingredients and finished products. We control the entire production process to ensure compliance with the highest standards of quality and safety.

We primarily serve business clients in the pharmaceutical, biotech, and healthcare industries. For individual customers, we recommend reaching out to our authorized distributors.

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