Ranitidine HCL IP pharma grade powder

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Product Details:

Structural Formula C13H22N4O3SHCl (structure available on request)
Heavy Metal (%) Not more than 0.001%
Solubility Freely soluble in water; slightly soluble in alcohol; practically insoluble in chloroform and in ether.
Loss on Drying Not more than 0.5%
Taste Bitter
HS Code 29349900
Shelf Life 3 Years
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Ranitidine HCL IP pharma grade powder Price And Quantity

Minimum Order Quantity 100 Kilograms

Ranitidine HCL IP pharma grade powder Product Specifications

Boiling point Not applicable (decomposes before boiling)
Ph Level 4.5 - 7.5 (5% solution)
Molecular Formula C13H22N4O3SHCl
Particle Size 25-80 Microns
Poisonous No (when handled as per pharma standards)
Color White to Off-White
Smell Odorless
Melting Point 134-140C
Storage Store in a cool, dry place, protected from light and moisture.
Shelf Life 3 Years
EINECS No 266-583-3
Molecular Weight 350.87 g/mol
Appearance White to Pale Yellow Crystalline Powder
Physical Form Powder
Grade IP (Indian Pharmacopoeia), Pharma Grade
Loss on Drying Not more than 0.5%
Type Pharmaceutical Raw Material
Medicine Name Ranitidine HCL
CAS No 66357-59-3
HS Code 29349900
Taste Bitter
Heavy Metal (%) Not more than 0.001%
Purity(%) >= 99%
Chemical Name N-[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylthio]ethyl]-N-methyl-2-nitroethene-1,1-diamine hydrochloride
Structural Formula C13H22N4O3SHCl (structure available on request)
Solubility Freely soluble in water; slightly soluble in alcohol; practically insoluble in chloroform and in ether.
Usage Used in the manufacture of antacid formulations; treatment of ulcers, GERD, and conditions of excessive stomach acid.

Residual Solvents Complies with ICH guidelines
Packaging Fibre drums with double polyethylene liner, 25 kg net weight or as required
Precautions Avoid inhalation and direct contact; use personal protective equipment while handling
Microbial Limits Complies with IP pharmacopeia
pKa Value 8.2
Application Area Pharmaceutical Formulations, Research & Development, Bulk Drug Manufacturing
Related Substances Not more than 0.3%
Identification Tests Complies with IP standards
Origin of Raw Material Synthetically manufactured
Assay (on dried basis) Between 98.5% and 101.0%

Ranitidine HCL IP pharma grade powder Trade Information

Supply Ability 1000 Kilograms Per Week
Delivery Time 7 Days

Product Description

Unlock an unrivaled promotion with our Ranitidine HCL IP Pharma Grade Powder, now available at a special rate for a limited offer. This praiseworthy, first-string pharmaceutical raw material boasts purity of 99%, a precise assay (98.5%-101.0%), and strictly complies with IP standards and ICH guidelines. Presented in secure fibre drums (25 kg net), it's perfectly suited for pharmaceutical formulations, R&D, and bulk drug manufacturing. Choose quality assurance backed by exceptional pharmacological credentials-your trusted partner for authentic, efficacious antacid production solutions.

Diverse Commercial Applications and Premium Usage

Ranitidine HCL IP pharma grade powder is an ideal choice for manufacturers and research entities engaged in antacid, ulcer, and GERD formulations. Its versatility extends to pharmaceutical R&D and bulk drug production, supporting a wide spectrum of application media. With high solubility in water and fine particle size, the formulation process is streamlined, ensuring superior product consistency across various drug delivery systems. Experience efficacy and dependable results with this pharmaceutical-grade material in all your commercial ventures.

FOB Port, Export Market Valuation, and Supply Capacity

Our Ranitidine HCL IP pharma grade powder is readily available for bulk export, shipped from major FOB ports in India. We ensure a consistent and reliable supply for both domestic and international markets, with an emphasis on quality and valuation compliance. Our robust distribution channels position us as a preferred supplier, trader, and wholesaler, supporting growing demands across global export markets while sustaining impeccable delivery and service standards for every consignment.

FAQ's of Ranitidine HCL IP pharma grade powder:

Q: How is Ranitidine HCL IP pharma grade powder typically used in pharmaceutical manufacturing?

A: Ranitidine HCL IP pharma grade powder is primarily used in the formulation of antacid preparations, treatment regimens for ulcers, GERD, and other conditions related to excessive stomach acid production. Pharmaceutical companies value its high purity and compliance with stringent regulatory standards for safe and effective drug manufacturing.

Q: What application areas benefit most from Ranitidine HCL IP powder?

A: This product is highly beneficial for pharmaceutical formulation, bulk drug manufacturing, and research and development sectors. Its extensive use in the creation of oral dosage forms, including tablets and suspensions, underscores its versatility in the pharmaceutical industry.

Q: Where is the raw material for Ranitidine HCL IP synthesized?

A: The raw material for Ranitidine HCL IP pharma grade powder is synthetically manufactured under controlled chemical processes, ensuring high consistency, purity, and compliance with pharmacopeial standards.

Q: What precautions should be taken while handling Ranitidine HCL IP powder?

A: Always avoid inhalation and direct contact when handling this powder. It is advisable to use appropriate personal protective equipment, such as gloves, masks, and safety glasses, within a controlled environment to maintain safety standards.

Q: How can clients order and receive supply of Ranitidine HCL IP pharma grade powder for export?

A: Clients can contact us directly for orders. Bulk quantities are shipped in fibre drums with double polyethylene liners from leading FOB ports in India. We ensure efficient and timely delivery to international and domestic markets with reliable supply chains.

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