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Allopurinol Structure

Product Type

API

Grade

BP/USP/EP

Chemical Formula

C5H4N4O

IUPAC Name

1H-pyrazolo[3,4-d] pyrimidin-4-ol

CAS No.

315-30-0

Molecular Weight

136.1115 g/mol

Chemical Class

Pyrazolo[3,4-d] pyrimidines

Therapeutic Class

Antigout

Synonyms

PHYSIOCHEMICAL PROPERTIES

Appearance White or almost white crystalline powder
Solubility soluble in DMSO (3 mg/ml), poorly soluble in water (0.1 mg/mL)
Melting point 320°C
pH 3.1- 3.4

Product Description

Allopurinol is a xanthine oxidase inhibitor used to reduce urinary and serum uric acid concentrations in patients with gout, recurrent calcium oxalate calculi, and various malignancies. Allopurinol is one of the most effective drugs used to decrease urate levels and is frequently used in the treatment of chronic gout.

How Allopurinol Works

Allopurinol and its active metabolite inhibit xanthine oxidase, the enzyme that converts hypoxanthine to xanthine and xanthine to uric acid. The inhibition of this enzyme is responsible for the effects of allopurinol. This drug increases the reutilization of hypoxanthine and xanthine for nucleotide and nucleic acid synthesis by a process that involves the enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRTase). This process results in an increased nucleotide concentration, which causes feedback inhibition of de novo purine synthesis. The end result is decreased urine and serum uric acid concentrations 15, which decreases the incidence of gout symptoms.

Use(s)

Adverse Effects

Why choose Salius for Allopurinol?

  1. Commitment to Global Quality Standards
    Salius upholds strict compliance with WHO-GMP guidelines across all manufacturing units, with select facilities additionally certified by the U.S. FDA. Each production batch undergoes thorough testing in advanced laboratories, reinforced by a robust internal quality assurance system to guarantee consistent safety and product integrity.
  2. Enhancing Cost Efficiency Through High-Volume API Supply
    Salius delivers high-quality Active Pharmaceutical Ingredients (APIs) at competitive global pricing. With strong capabilities in large-scale manufacturing and export, Salius supports cost-effective sourcing and reliable supply — a key advantage for pharmaceutical companies in price-sensitive markets.
  3. Global Export Expertise and Comprehensive Documentation Support
    Salius has experience exporting APIs worldwide, offering full regulatory documentation including Drug Master Files (DMF) and impurity profiles. We provide dedicated support for regulatory filings to help international clients, even in highly regulated markets, ensure smooth approval and compliance.
  4. Documents We Provide
  5. Proven Reliability
    Salius Pharma is presented as a government-recognized star export house with strong quality and delivery ratings.
Attribute Why Salius Pharma Is a Good Choice
Quality Certification WHO-GMP, ISO 9001:2015, FDA-audited facilities
Affordability & Generic Access Cost-competitive generics for global supply
Export Experience Proven record of supplying globally

What You Receive in Our Package

When you order from Salius Pharma, you receive more than just a product — you receive a complete, professionally prepared package that meets international regulatory and quality expectations.

Each Shipment Includes:

Product

Expected Delivery Time

We ensure prompt and reliable shipping worldwide. Delivery times vary depending on destination, order volume, and regulatory requirements.

Overall Delivery Time:

7 to 21 business days from dispatch, depending on your location.

FAQs

In Latin America, Allopurinol is widely used to manage gout and hyperuricemia (high uric acid levels). It helps reduce the production of uric acid in the body, preventing gout attacks and complications such as kidney stones.

Yes, common side effects include skin rash, nausea, and drowsiness. In rare cases, more serious reactions can occur. It’s important to follow your doctor’s instructions and report any unusual symptoms.

Salius Pharma supplies Allopurinol as a bulk API (Active Pharmaceutical Ingredient). Upon request, we can also provide finished dosage forms such as tablets, tailored to the regulatory standards of Latin American markets.

To place an order, contact Salius Pharma with details such as required quantity, destination country in Latin America, and documentation needs like WHO-GMP certification, Certificate of Analysis, or Drug Master File (DMF). Our team will guide you through the process.

Salius Pharma supplies Allopurinol to several Latin American countries, including Peru, Ecuador, Bolivia, Guatemala, and the Dominican Republic, supporting local pharmaceutical production and formulation.

Place an Order or Request a Quote

Looking to source Allopurinol or other high-quality pharmaceutical products? We’re here to help. Whether you need Active Pharmaceutical Ingredients (APIs), finished formulations, or regulatory support, our team is ready to provide dependable, compliant, and cost-effective solutions tailored to your market needs.

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