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Quiniodochlor IP WHO GMP

Quiniodochlor IP WHO GMP

Product Details:

  • EINECS No 201-496-9
  • Particle Size Passes through 120 mesh
  • Heavy Metal (%) Not more than 0.002%
  • Taste Bitter
  • Melting Point 175-180C
  • Solubility Slightly soluble in water, soluble in dilute acids and alkalis
  • Smell Odorless
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Quiniodochlor IP WHO GMP Price And Quantity

  • 100 Kilograms

Quiniodochlor IP WHO GMP Product Specifications

  • C9H5ClINO
  • Powder
  • Quiniodochlor IP WHO GMP
  • Non-poisonous as per IP
  • Pharmaceutical Formulation
  • 83-73-8
  • 98% Min
  • Yellow to greenish-yellow crystalline powder
  • Yellow to greenish-yellow
  • C9H5ClINO
  • IP, WHO GMP
  • Store in a cool, dry place, protected from light
  • Not more than 1.0%
  • 5 years from date of manufacture
  • 2933.39.19
  • 305.5 g/mol
  • Odorless
  • Slightly soluble in water, soluble in dilute acids and alkalis
  • Active Pharmaceutical Ingredient
  • 175-180C
  • Bitter
  • Not more than 0.002%
  • Passes through 120 mesh
  • 201-496-9
  • 5-Chloro-7-iodo-8-quinolinol
  • 98.0% to 101.0%
  • Complies with IP tests
  • Meets IP standards
  • HDPE drums with double polythene liners / as required
  • Complies with IP

Quiniodochlor IP WHO GMP Trade Information

  • 1000 Kilograms Per Month
  • 7 Days

Product Description



Experience the illustrious quality of Quiniodochlor IP WHO GMP, an ultimate Active Pharmaceutical Ingredient meticulously designed for pharmaceutical formulation. Presented in special HDPE drums with double polythene liners, this product offers soaring purity, registering 98.0% to 101.0% assay on a dry basis and meeting all IP standards for related substances and residual solvents. Utilise offers that ensure you benefit from this ephemeral, high-grade API with unmatched stability, appearance, and chemical integrity. Secure your stock through our trusted distribution network and elevate your pharmaceutical endeavors.

Applications and Features of Quiniodochlor IP WHO GMP

Widely used by pharmaceutical manufacturers, Quiniodochlor IP WHO GMP is ideal for fabricating safe and effective formulations. The product features a crystalline powder form, yellow to greenish-yellow in color, with odorless, bitter characteristics. Passing through a 120 mesh sieve, it ensures uniformity for precise blending. Apply it on pharmaceutical-grade machinery and surfaces, offering optimal consistency and compliance with stringent industry standards for active ingredients.


Certifications, Export Logistics, and Delivery Details

Our Quiniodochlor IP WHO GMP is certified to comply with IP and WHO GMP standards, cementing its place among the industry's most trusted APIs. With flexible delivery and exchange options via major Indian FOB ports, we ensure your logistics needs are seamlessly met. Our main export markets encompass Asia, Africa, and the Middle East, guaranteeing timely response and efficient transport to various global destinations.


FAQ's of Quiniodochlor IP WHO GMP:


Q: How is Quiniodochlor IP WHO GMP typically used in pharmaceutical formulations?

A: Quiniodochlor IP WHO GMP is utilised as an active pharmaceutical ingredient in the manufacturing of medications, contributing to the desired therapeutic properties in the finished products.

Q: What is the process for ensuring product identification and purity?

A: Each batch of Quiniodochlor IP WHO GMP is tested to comply with IP standards for identification, assay, related substances, and residual solvents, ensuring high purity and consistent quality.

Q: When should Quiniodochlor IP WHO GMP be stored to maintain potency?

A: For best results, store Quiniodochlor IP WHO GMP in a cool, dry place protected from light to preserve its quality and extend its five-year shelf life.

Q: Where can Quiniodochlor IP WHO GMP be exported from?

A: The product is exported from India, with shipments coordinated through major FOB ports, ensuring efficient delivery to global destinations.

Q: What are the benefits of using a WHO GMP certified Quiniodochlor IP?

A: Utilising a WHO GMP certified product guarantees compliance with global safety and efficacy standards, offering assurance of premium quality and regulatory acceptance in pharmaceutical markets.

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