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Pyrantel Pamoate USP raw material
Pyrantel Pamoate USP raw material
Pyrantel Pamoate USP raw material
Pyrantel Pamoate USP raw material
Pyrantel Pamoate USP raw material
Pyrantel Pamoate USP raw material
Pyrantel Pamoate USP raw material
Pyrantel Pamoate USP raw material
Pyrantel Pamoate USP raw material
Pyrantel Pamoate USP raw material
Pyrantel Pamoate USP raw material
Pyrantel Pamoate USP raw material

Pyrantel Pamoate USP raw material

Price 36000 INR/ Kilograms

MOQ : 100 Kilograms

Pyrantel Pamoate USP raw material Specification

  • Storage
  • Store in a tightly closed container. Keep in a cool, dry place, protected from light.
  • Shelf Life
  • 5 years
  • Smell
  • Odorless
  • HS Code
  • 29339900
  • Color
  • Yellow to orange
  • Melting Point
  • 133-136C
  • Structural Formula
  • [Refer to chemical structure diagram in chemical literature]
  • Boiling point
  • Not applicable (decomposes)
  • Taste
  • Bitter
  • Solubility
  • Practically insoluble in water, soluble in alcohol, chloroform and dilute mineral acids
  • EINECS No
  • 244-837-1
  • Heavy Metal (%)
  • 0.002%
  • Particle Size
  • 90% passes through 100 mesh
  • Molecular Weight
  • 594.70 g/mol
  • Molecular Formula
  • C11H14N2SC23H16O6
  • Poisonous
  • Non-poisonous at therapeutic doses
  • Ph Level
  • pH (1% suspension): 6.0-7.5
  • Loss on Drying
  • 5.0%
  • Medicine Name
  • Pyrantel Pamoate USP
  • Chemical Name
  • (E)-1,4,5,6-tetrahydro-1-methyl-2-(2-thienylcarbonyl)pyrimidine pamoate
  • CAS No
  • 22204-24-6
  • Type
  • Anthelmintic Active Pharmaceutical Ingredient
  • Grade
  • USP
  • Usage
  • Used for treatment of intestinal worm infections
  • Purity(%)
  • 98%
  • Appearance
  • Yellow to orange crystalline powder
  • Physical Form
  • Solid
  • Packing
  • Drum with double PE bags, 25 kg net
  • Endotoxins
  • <0.25 EU/mg
  • Identification
  • Complies with USP tests (IR, HPLC, chemical tests)
  • Microbial Limits
  • Total aerobic microbial count 1000 cfu/g, Total yeast and mold 100 cfu/g
  • Residual Solvents
  • Complies with USP <467> limits
  • Assay (HPLC)
  • 98.0% - 102.0%
  • Bulk Density
  • 0.30 - 0.50 g/cm3
  • Specific Optical Rotation
  • Not more than 5
  • Stability
  • Stable under recommended storage conditions
  • Related Substances
  • Total impurities 1.0%
 

Pyrantel Pamoate USP raw material 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
 

About Pyrantel Pamoate USP raw material



Experience the fresh excellence of Pyrantel Pamoate USP-an opulent anthelmintic raw material designed for pharmaceutical brilliance. Highlighted by a magnificent purity of 98% (HPLC), this must-have ingredient boasts impeccable compliance with USP standards for identification, residual solvents, and related substances. Its stability and broad-spectrum efficacy render it perfect for intestinal worm treatments, offering a solid, yellow to orange crystalline powder form. With magnificent control over microbial and impurity limits, this product assures exceptional safety for your pharmaceutical innovations. An essential addition for manufacturers demanding quality and reliability.

Versatile Application for Anthelmintic Treatment

Pyrantel Pamoate USP is a premium active pharmaceutical ingredient (API) specially designed for the treatment of intestinal worm infections. This raw material finds use in oral solid dosage forms such as tablets and suspensions. The key site of application is the gastrointestinal tract, where it acts effectively against common parasites. Utilized by pharmaceutical and veterinary manufacturers, it is an indispensable ingredient for health solutions addressing parasitic infections.


Certifications, Export Markets, and Pricing Information

This product is USP certified and comes with compliance documentation for all relevant specifications. Our list price reflects the supreme quality and safety standards maintained throughout production. Pyrantel Pamoate USP is exported to major markets worldwide, with India as a leading distribution hub. FOB port services from Mumbai and other major Indian ports are available, with efficient freight and transportation options arranged for global shipping. Our robust supply network supports consistent export to distributors and wholesalers internationally.


FAQ's of Pyrantel Pamoate USP raw material:


Q: How is Pyrantel Pamoate USP best stored to ensure stability?

A: Pyrantel Pamoate USP should be stored in a tightly closed container, kept in a cool, dry place, and protected from light to maintain its stability and efficacy throughout its 5-year shelf life.

Q: What are the primary benefits of using Pyrantel Pamoate USP in pharmaceutical formulations?

A: The primary benefits include its high assay purity of 98%-102%, compliance with strict USP microbial and residual solvent limits, and targeted anthelmintic effectiveness for treating intestinal worms.

Q: Where is Pyrantel Pamoate USP typically applied in formulations?

A: It is primarily used in oral solid dosage forms like tablets and suspensions, specifically targeting the gastrointestinal tract to combat parasitic infections.

Q: What testing and certifications does Pyrantel Pamoate USP comply with?

A: Pyrantel Pamoate USP complies with USP identification tests (IR, HPLC, chemical), residual solvents test USP <467>, related substances, microbial limits, and is supplied with all supporting certifications.

Q: When should manufacturers opt for Pyrantel Pamoate USP raw material?

A: Manufacturers should choose Pyrantel Pamoate USP when creating medicines aimed at intestinal worm infections, seeking a purified, safe, and stable API to ensure product efficacy and regulatory compliance.

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