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Quiniodochlor IP API with DMF

Quiniodochlor IP API with DMF

Product Details:

  • Solubility Slightly soluble in water, soluble in alcohol and chloroform
  • Molecular Weight 305.50 g/mol
  • Taste Bitter
  • HS Code 2933.49
  • Storage Store in a well-closed container, protected from light and moisture
  • Boiling point Not applicable (decomposes)
  • Ph Level 5.0 - 7.0 (1% solution in water)
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Quiniodochlor IP API with DMF Price And Quantity

  • 100 Kilograms

Quiniodochlor IP API with DMF Product Specifications

  • 305.50 g/mol
  • Bitter
  • Slightly soluble in water, soluble in alcohol and chloroform
  • 83-73-8
  • >=98%
  • Store in a well-closed container, protected from light and moisture
  • 2933.49
  • Used in pharmaceutical formulations as an intestinal antiseptic
  • Solid
  • 8-Hydroxy-7-iodo-5-quinolinesulfonic acid
  • 90% passes through 100 mesh
  • Not applicable (decomposes)
  • 5.0 - 7.0 (1% solution in water)
  • Quiniodochlor IP API with DMF
  • Odorless
  • 201-496-0
  • 3 years from the date of manufacture, if stored properly
  • Active Pharmaceutical Ingredient (API)
  • Not classified as poisonous under standard conditions; may be toxic at high doses
  • White to yellowish crystalline powder
  • (See product image for structural diagram)
  • White to pale yellow
  • <0.001%
  • IP (Indian Pharmacopoeia)
  • 180-185C
  • 0.5%
  • C9H5ClINO
  • Ambient, avoid excessive heat and moisture
  • Complies with IP limits (NMT 1.0%)
  • HDPE drum with double polyethylene bags
  • DMF, GMP, and COA available
  • >=98%
  • Complies as per IP specification
  • Conforms to standard
  • Available on request
  • Available
  • GMP Certified
  • Within ICH limits
  • Provided with each batch

Quiniodochlor IP API with DMF Trade Information

  • 1000 Kilograms Per Month
  • 7 Days

Product Description



Unlock the potential of our new, best-seller Quiniodochlor IP API with DMF-crafted for unassailable quality and flawless results in pharmaceutical formulations. This resplendent ingredient, also known as 8-Hydroxy-7-iodo-5-quinolinesulfonic acid, meets stringent IP standards with 98% purity, low heavy metal content (<0.001%), and residual solvents within ICH regulations. Every batch is GMP certified, comes with a comprehensive Certificate of Analysis, and is expertly packaged in HDPE drums. Stability data and Drug Master File documentation are readily available, ensuring your projects benefit from unwavering reliability.

Quiniodochlor IP API with DMF: Usage and Features

Quiniodochlor IP API with DMF is essential for pharmaceutical manufacturers as an intestinal antiseptic. Renowned for its flawless purity, it is delivered as a white to yellowish crystalline powder. Its applications span intestinal antiseptic formulations, adhering to IP norms and GMP-certified processes. With a high assay (98%), remarkable stability, and reliable compliance with stringent microbial and residual solvent specifications, this pharmaceutical API is tailored for quality-driven export and domestic supply requirements.


Payment Terms, Sample Policy, and Export Information

Packing & Dispatch of Quiniodochlor IP API with DMF prioritizes safety-utilizing double polyethylene bags in HDPE drums. Purchase Orders are seamlessly processed, and dispatch is arranged under ambient transportation, with goods safeguarded against excessive heat or moisture. Sample policies are flexible, catering to client assurance needs. Our main export markets span India, Asia, Africa, and more, with streamlined goods transport ensuring prompt deliveries and competitive global service.


FAQ's of Quiniodochlor IP API with DMF:


Q: How should Quiniodochlor IP API with DMF be stored to maintain its flawless quality?

A: Quiniodochlor IP API with DMF should be stored in a well-closed container, protected from light and moisture, at ambient temperature to preserve its integrity for up to three years.

Q: What is the main usage of Quiniodochlor IP API with DMF in pharmaceuticals?

A: It is primarily used as an intestinal antiseptic in various pharmaceutical formulations, valued for its resplendent purity and reliable compliance with pharmacopoeial standards.

Q: When is a Certificate of Analysis (COA) provided for each batch?

A: A detailed Certificate of Analysis is provided with every batch, ensuring that each delivery meets the expected identity, purity, and quality standards.

Q: Where is Quiniodochlor IP API with DMF mainly exported or supplied from?

A: We distribute, export, and supply Quiniodochlor IP API with DMF from India, serving clients across Asia, Africa, and global markets.

Q: What is the process for obtaining stability data and DMF documentation?

A: Stability data and Drug Master File documentation are available on request; simply mention your requirements when placing a Purchase Order or inquiry.

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