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Ranitidine HCL IP pharma grade powder

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MOQ : 100 Kilograms

Ranitidine HCL IP pharma grade powder Specification

Shelf Life
3 Years

Melting Point
134-140C

Loss on Drying
Not more than 0.5%

Solubility
Freely soluble in water; slightly soluble in alcohol; practically insoluble in chloroform and in ether.

Particle Size
25-80 Microns

EINECS No
266-583-3

Ph Level
4.5 - 7.5 (5% solution)

Smell
Odorless

Structural Formula
C13H22N4O3SHCl (structure available on request)

HS Code
29349900

Molecular Weight
350.87 g/mol

Boiling point
Not applicable (decomposes before boiling)

Taste
Bitter

Poisonous
No (when handled as per pharma standards)

Molecular Formula
C13H22N4O3SHCl

Color
White to Off-White

Heavy Metal (%)
Not more than 0.001%

Storage
Store in a cool, dry place, protected from light and moisture.

Medicine Name
Ranitidine HCL

Chemical Name
N-[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylthio]ethyl]-N-methyl-2-nitroethene-1,1-diamine hydrochloride

CAS No
66357-59-3

Type
Pharmaceutical Raw Material

Grade
IP (Indian Pharmacopoeia), Pharma Grade

Usage
Used in the manufacture of antacid formulations; treatment of ulcers, GERD, and conditions of excessive stomach acid.

Purity(%)
>= 99%

Appearance
White to Pale Yellow Crystalline Powder

Physical Form
Powder

Assay (on dried basis)
Between 98.5% and 101.0%

Identification Tests
Complies with IP standards

Application Area
Pharmaceutical Formulations, Research & Development, Bulk Drug Manufacturing

Origin of Raw Material
Synthetically manufactured

Microbial Limits
Complies with IP pharmacopeia

Related Substances
Not more than 0.3%

pKa Value
8.2

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

Ranitidine HCL IP pharma grade powder Trade Information

Minimum Order Quantity
100 Kilograms

Supply Ability
1000 Kilograms Per Week

Delivery Time
7 Days

About Ranitidine HCL IP pharma grade powder

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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