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Pyrantel Pamoate USP raw material

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MOQ : 100 Kilograms

Pyrantel Pamoate USP raw material Specification

Loss on Drying
5.0%

Molecular Weight
594.70 g/mol

Smell
Odorless

Storage
Store in a tightly closed container. Keep in a cool, dry place, protected from light.

Structural Formula
[Refer to chemical structure diagram in chemical literature]

Boiling point
Not applicable (decomposes)

Taste
Bitter

Melting Point
133-136C

HS Code
29339900

Ph Level
pH (1% suspension): 6.0-7.5

EINECS No
244-837-1

Poisonous
Non-poisonous at therapeutic doses

Shelf Life
5 years

Particle Size
90% passes through 100 mesh

Molecular Formula
C11H14N2SC23H16O6

Heavy Metal (%)
0.002%

Solubility
Practically insoluble in water, soluble in alcohol, chloroform and dilute mineral acids

Color
Yellow to orange

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

Identification
Complies with USP tests (IR, HPLC, chemical tests)

Stability
Stable under recommended storage conditions

Microbial Limits
Total aerobic microbial count 1000 cfu/g, Total yeast and mold 100 cfu/g

Endotoxins
<0.25 EU/mg

Specific Optical Rotation
Not more than 5

Assay (HPLC)
98.0% - 102.0%

Related Substances
Total impurities 1.0%

Bulk Density
0.30 - 0.50 g/cm3

Residual Solvents
Complies with USP <467> limits

Pyrantel Pamoate USP raw material Trade Information

Minimum Order Quantity
100 Kilograms

Supply Ability
1000 Kilograms Per Month

Delivery Time
7 Days

Pyrantel Pamoate USP raw material About

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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