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Pyrantel Pamoate USP API with DMF

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MOQ : 100 Kilograms

Pyrantel Pamoate USP API with DMF Specification

Shelf Life
36 months

Melting Point
> 200C (decomposes)

Solubility
Practically insoluble in water, freely soluble in chloroform and methanol

Loss on Drying
NMT 0.5%

EINECS No
244-837-1

Smell
Odorless

Poisonous
Non-poisonous, if used as directed

Color
Yellow

HS Code
29349900

Storage
Store in a tightly closed container, protected from light and moisture at room temperature

Molecular Formula
C34H30N2O6S

Molecular Weight
594.68 g/mol

Structural Formula
Available on request

Heavy Metal (%)
NMT 0.001%

Boiling point
Not applicable (decomposes before boiling)

Ph Level
6.5 - 7.5 (1% solution in water)

Particle Size
D90 < 40 microns

Medicine Name
Pyrantel Pamoate USP API with DMF

Chemical Name
(E)-1,4,5,6-tetrahydro-1-methyl-2-(2-thienylcarbonyl)pyrimidine-4,4-pamoate

CAS No
22204-24-6

Type
Active Pharmaceutical Ingredient (API)

Grade
USP

Usage
Anthelmintic/Used for the treatment of intestinal worm infections

Purity(%)
>=99%

Appearance
Fine Yellow Powder

Physical Form
Solid

Impurities
Within USP limits

Assay (On dried basis)
>=99.0% (by HPLC)

Residual Solvents
Complies with USP requirements

Manufacturer Certification
GMP, WHO-GMP, ISO 9001:2015

DMF Status
Available (Drug Master File Registered)

Controls
Particle size test, Bulk density, Tap density, Individual impurity test

Microbial Limits
Total aerobic microbial count: NMT 1000 CFU/g, Total combined yeasts and molds: NMT 100 CFU/g

Packaging
HDPE drums with double polyethylene liners, 25 kg net

Stability
Stable under recommended storage conditions

Identification
Complies with USP Standards (IR, HPLC)

End Application
Pharmaceutical formulations (tablets, suspensions, chewable tablets, oral solutions)

Pyrantel Pamoate USP API with DMF Trade Information

Minimum Order Quantity
100 Kilograms

Supply Ability
1000 Kilograms Per Month

Delivery Time
7 Days

Pyrantel Pamoate USP API with DMF About

Pyrantel Pamoate USP API with DMF is a best-seller, acclaimed for its sterling quality and gilt-edged compliance with USP standards. Offered at a reduced price, it is a first-class, non-poisonous active pharmaceutical ingredient for anthelmintic use in treating intestinal worm infections. Manufactured under strict GMP and WHO-GMP guidelines, it boasts a purity of 99% and outstanding stability for 36 months. The API meets all regulatory specifications-DMF registered, impurities within USP limits, and comprehensive testing for bulk density, individual impurity, and particle size, ensuring top-tier pharmaceutical reliability.

Advantages & Features of Pyrantel Pamoate USP API with DMF

Pyrantel Pamoate USP API with DMF offers distinct advantages, such as its exceptional assay of 99.0% and compliance with all USP standards. The fine yellow powder is practically insoluble in water, yet freely soluble in chloroform and methanol. Special features include robust particle size control, stringent bulk and tap density testing, and comprehensive impurity assessments. Its stability under recommended storage conditions and non-poisonous profile set it apart for high-quality pharmaceutical formulations.

Packaging Details, Payment Terms & Sample Availability

This first-class API is securely packed in HDPE drums with double polyethylene liners, 25 kg net, ensuring a safe drop-off. Express shipping and global distribution are available. Flexible payment terms are offered for convenience, and product samples can be arranged on request, with a nominal charge. Whether you're a distributor or manufacturer, our streamlined logistics ensure prompt delivery and reliability for every order.

FAQ's of Pyrantel Pamoate USP API with DMF:

Q: How is the quality of Pyrantel Pamoate USP API with DMF assured?

A: The API fully complies with USP standards, features a DMF registration, and undergoes comprehensive tests, including assay (99.0%), impurity analysis, and microbial limits, ensuring sterling, first-class quality.

Q: What pharmaceutical applications is Pyrantel Pamoate USP API suitable for?

A: It is used in manufacturing tablets, chewable tablets, suspensions, and oral solutions for the treatment of intestinal worm infections.

Q: Where is Pyrantel Pamoate USP API manufactured and supplied from?

A: The API is manufactured and supplied in India by GMP, WHO-GMP, and ISO 9001:2015 certified facilities, catering to distributors, exporters, importers, and wholesalers globally.

Q: What are the packaging and shipping options for this API?

A: Pyrantel Pamoate USP API is packaged in 25 kg HDPE drums with double polyethylene liners for secure drop-off and express shipping to various locations.