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Quiniodochlor IP API with DMF

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MOQ : 100 Kilograms

Quiniodochlor IP API with DMF Specification

Smell
Odorless

Structural Formula
(See product image for structural diagram)

Melting Point
180-185C

Solubility
Slightly soluble in water, soluble in alcohol and chloroform

Poisonous
Not classified as poisonous under standard conditions; may be toxic at high doses

Molecular Weight
305.50 g/mol

Heavy Metal (%)
<0.001%

Ph Level
5.0 - 7.0 (1% solution in water)

Storage
Store in a well-closed container, protected from light and moisture

Boiling point
Not applicable (decomposes)

Shelf Life
3 years from the date of manufacture, if stored properly

Particle Size
90% passes through 100 mesh

Taste
Bitter

EINECS No
201-496-0

Loss on Drying
0.5%

HS Code
2933.49

Molecular Formula
C9H5ClINO

Color
White to pale yellow

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

Microbial Limits
Complies as per IP specification

Related Substances
Complies with IP limits (NMT 1.0%)

Packaging
HDPE drum with double polyethylene bags

Documentation
DMF, GMP, and COA available

Certificate of Analysis (COA)
Provided with each batch

Residual Solvents
Within ICH limits

Transportation Condition
Ambient, avoid excessive heat and moisture

Assay (By Titration/UV)
>=98%

Stability Data
Available on request

Manufacturing Standard
GMP Certified

DMF (Drug Master File) Status
Available

Identity (By IR)
Conforms to standard

Quiniodochlor IP API with DMF Trade Information

Minimum Order Quantity
100 Kilograms

Supply Ability
1000 Kilograms Per Month

Delivery Time
7 Days

Quiniodochlor IP API with DMF About

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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