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Quiniodochlor IP API with DMF
Quiniodochlor IP API with DMF
Quiniodochlor IP API with DMF
Quiniodochlor IP API with DMF
Quiniodochlor IP API with DMF
Quiniodochlor IP API with DMF
Quiniodochlor IP API with DMF
Quiniodochlor IP API with DMF
Quiniodochlor IP API with DMF
Quiniodochlor IP API with DMF
Quiniodochlor IP API with DMF
Quiniodochlor IP API with DMF

Quiniodochlor IP API with DMF

Price 3600 INR/ Kilograms

MOQ : 100 Kilograms

Quiniodochlor IP API with DMF Specification

  • Molecular Formula
  • C9H5ClINO
  • Structural Formula
  • (See product image for structural diagram)
  • Ph Level
  • 5.0 - 7.0 (1% solution in water)
  • Boiling point
  • Not applicable (decomposes)
  • Smell
  • Odorless
  • Melting Point
  • 180-185C
  • Taste
  • Bitter
  • Storage
  • Store in a well-closed container, protected from light and moisture
  • Molecular Weight
  • 305.50 g/mol
  • Color
  • White to pale yellow
  • Loss on Drying
  • 0.5%
  • Heavy Metal (%)
  • <0.001%
  • Particle Size
  • 90% passes through 100 mesh
  • Shelf Life
  • 3 years from the date of manufacture, if stored properly
  • HS Code
  • 2933.49
  • Solubility
  • Slightly soluble in water, soluble in alcohol and chloroform
  • Poisonous
  • Not classified as poisonous under standard conditions; may be toxic at high doses
  • EINECS No
  • 201-496-0
  • Medicine Name
  • Quiniodochlor IP API with DMF
  • Chemical Name
  • 8-Hydroxy-7-iodo-5-quinolinesulfonic acid
  • CAS No
  • 83-73-8
  • Type
  • Active Pharmaceutical Ingredient (API)
  • Grade
  • IP (Indian Pharmacopoeia)
  • Usage
  • Used in pharmaceutical formulations as an intestinal antiseptic
  • Purity(%)
  • >=98%
  • Appearance
  • White to yellowish crystalline powder
  • Physical Form
  • Solid
  • Related Substances
  • Complies with IP limits (NMT 1.0%)
  • Manufacturing Standard
  • GMP Certified
  • Transportation Condition
  • Ambient, avoid excessive heat and moisture
  • DMF (Drug Master File) Status
  • Available
  • Residual Solvents
  • Within ICH limits
  • Identity (By IR)
  • Conforms to standard
  • Packaging
  • HDPE drum with double polyethylene bags
  • Microbial Limits
  • Complies as per IP specification
  • Certificate of Analysis (COA)
  • Provided with each batch
  • Assay (By Titration/UV)
  • >=98%
  • Stability Data
  • Available on request
  • Documentation
  • DMF, GMP, and COA available
 

Quiniodochlor IP API with DMF Trade Information

  • Minimum Order Quantity
  • 100 Kilograms
  • FOB Port
  • mudara
  • Payment Terms
  • Cash Advance (CA), Cash in Advance (CID), Letter of Credit at Sight (Sight L/C), Letter of Credit (L/C)
  • Supply Ability
  • 1000 Kilograms Per Month
  • Delivery Time
  • 7 Days
  • Sample Available
  • Yes
  • Sample Policy
  • If order is confirmed we will reimburse the sample cost
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • Main Domestic Market
  • , All India, South India, Central India, West India, North India, East India, Gujarat, Karnataka, Kerala, Lakshadweep, Mizoram, Meghalaya, Manipur, Andhra Pradesh, Bihar, Chandigarh, Daman and Diu, Goa, Jharkhand, Odisha, Punjab, Assam
 

About Quiniodochlor IP API with DMF



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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