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Ranitidine HCL IP pharmaceutical raw material
Ranitidine HCL IP pharmaceutical raw material

Ranitidine HCL IP pharmaceutical raw material

MOQ : 100 Kilograms

Ranitidine HCL IP pharmaceutical raw material Specification

  • Particle Size
  • As per specification (usually 100% passes through 60 mesh)
  • HS Code
  • 29420090
  • Melting Point
  • 140-144C
  • Molecular Weight
  • 350.87 g/mol
  • Shelf Life
  • 5 years when properly stored
  • Color
  • White to pale yellow
  • Solubility
  • Freely soluble in water, sparingly soluble in alcohol
  • Taste
  • Slightly bitter
  • EINECS No
  • 266-583-0
  • Structural Formula
  • Refer to product literature for detailed structure
  • Storage
  • Store in cool, dry place, protected from light
  • Loss on Drying
  • 0.5%
  • Molecular Formula
  • C13H22N4O3SHCl
  • Ph Level
  • Approximately 6.0-7.0 (1% solution)
  • Poisonous
  • Non-poisonous under recommended usage
  • Smell
  • Odorless
  • Boiling point
  • Not applicable (decomposes)
  • Heavy Metal (%)
  • 0.001%
  • Medicine Name
  • Ranitidine HCL IP
  • Chemical Name
  • N-(2-((5-[(dimethylamino)methyl]furan-2-yl)methylthio)ethyl)-N-methyl-2-nitroethene-1,1-diamine hydrochloride
  • CAS No
  • 66357-35-5
  • Type
  • Pharmaceutical Raw Material
  • Grade
  • IP (Indian Pharmacopoeia)
  • Usage
  • Used in the formulation of antiulcer medications and acid reducers
  • Purity(%)
  • 99% min
  • Appearance
  • White to pale yellow crystalline powder
  • Physical Form
  • Solid
  • Residual Solvents
  • Complies with ICH guidelines
  • Specific Optical Rotation
  • As per IP specifications
  • Chloride Content
  • Within pharmacopoeial limits
  • Identification
  • Complies with IP tests
  • Assay (by HPLC)
  • Not less than 99.0% and not more than 101.0%
  • Related Substances
  • Meets IP requirements
  • Packing
  • HDPE drums with double polyethylene inner bag, 25 kg net wt.
  • Endotoxin Level
  • Less than 0.25 EU/mg
  • Microbial Limits
  • Complies as per IP standards
 

Ranitidine HCL IP pharmaceutical raw material Trade Information

  • Minimum Order Quantity
  • 100 Kilograms
  • Supply Ability
  • 1000 Kilograms Per Week
  • Delivery Time
  • 7 Days
 

Ranitidine HCL IP pharmaceutical raw material About



Ranitidine HCL IP pharmaceutical raw material is a top-quality, praiseworthy selection for those seeking an enlightened choice in antiulcer and acid reducer formulation. With uncommon purity (minimum 99%), this product complies with special IP and ICH guidelines, ensuring residual solvents, microbial, and heavy metal content remain within pharmacopoeial limits. Each batch undergoes rigorous identification and related substance checks. Packed securely in HDPE drums with double polyethylene liners, this limited stock is odorless, non-poisonous under recommended use, and ready for pharmaceutical manufacturing needs. Secure your supply while stock lasts!

Distinguished Features and Specialized Usage

Ranitidine HCL IP stands out with its high purity, impressive 5-year shelf life, and adherence to IP (Indian Pharmacopoeia) specifications. Uncommon solubility in water and strict microbial safety make it a special choice for medicine manufacturers. Primarily used in creating antiulcer drugs and acid reducers, its slightly bitter, odorless powder form ensures easy formulation. With its stable pH and low moisture content, it provides consistent results for distributors, importers, and exporters alike.


Convenient Payment, Immediate Shipping, and Smooth Delivery

Payment for Ranitidine HCL IP can be arranged via secure channels matched to buyer preference. Once orders are confirmed, goods are efficiently shipped out, ensuring prompt delivery across India and overseas destinations. Samples can be provided for quality verification prior to final purchase. Your consignment will be packed to top standards for safe goods transport, and the entire process is designed for reliability and customer satisfaction.


FAQ's of Ranitidine HCL IP pharmaceutical raw material:


Q: How is the quality of Ranitidine HCL IP pharmaceutical raw material ensured?

A: Each batch of Ranitidine HCL IP complies with Indian Pharmacopoeia (IP) and ICH guidelines. Parameters like assay, residual solvents, chloride content, microbial limits, and related substances are meticulously tested, ensuring exceptional purity and safety.

Q: What specific uses does Ranitidine HCL IP have in pharmaceutical manufacturing?

A: Ranitidine HCL IP is mainly used as a raw material in the formulation of antiulcer medications and acid reducers, trusted for its purity, stability, and performance in solid dosage development.

Q: Where can I purchase or request samples of Ranitidine HCL IP?

A: You can purchase or request samples directly through the manufacturer, authorized distributors, or suppliers listed across India and global export markets. Samples are available for quality assessment prior to bulk ordering.

Q: What are the shipping and delivery timelines for Ranitidine HCL IP?

A: Orders are promptly processed and shipped according to your delivery location and requirements. Standard packing ensures safe goods transport, and most shipments are dispatched within a few business days after payment confirmation.

Q: How should Ranitidine HCL IP be stored for optimal stability?

A: Store Ranitidine HCL IP in a cool, dry place protected from light. When stored under recommended conditions, it retains shelf life and quality for up to five years.

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