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Lafutidine

Lafutidine
Lafutidine

Lafutidine Specification

  • Heavy Metal (%)
  • Not more than 0.001%
  • HS Code
  • 29349900
  • Smell
  • Odorless
  • Solubility
  • Freely soluble in dimethyl sulfoxide (DMSO), sparingly soluble in water
  • Loss on Drying
  • Not more than 0.5%
  • Melting Point
  • 158-160C
  • Molecular Formula
  • C22H29N3O3S
  • Storage
  • Store in a cool, dry place, away from direct sunlight
  • Poisonous
  • NO
  • Shelf Life
  • 5 Years
  • Structural Formula
  • See image/structure provided
  • Color
  • White to off-white
  • Molecular Weight
  • 415.55 g/mol
  • Medicine Name
  • Lafutidine
  • Chemical Name
  • 2-[furfurylsulfinyl)-N-(4-(piperidinomethyl)-2-pyridyl)acetamide
  • CAS No
  • 118288-08-7
  • Type
  • Other
  • Grade
  • Other
  • Usage
  • Used as anti-ulcer agent, H2 receptor antagonist
  • Purity(%)
  • >=99.0%
  • Appearance
  • White to off-white crystalline powder
  • Physical Form
  • Solid
  • Stability
  • Stable under recommended storage conditions
  • Impurities
  • Complies with pharmacopoeial standards
  • Formulation
  • Bulk API material
  • Storage Temperature
  • 2-8°C recommended
  • Packing
  • HDPE drum or as per customer requirement
  • Pharmaceutical Grade
  • Complies with in-house specification and/or pharmacopoeial requirements
 

Lafutidine Trade Information

  • Minimum Order Quantity
  • 1 Kilograms
  • Supply Ability
  • 2000 Kilograms Per Day
  • Delivery Time
  • 1 Days
 

About Lafutidine

Lafutidine is a generic antihistamine drug which is used to treat diseases involving the gastrointestinal tract such as oesophagus, stomach, small intestine, large intestine, rectum etc., It is a histamine H2-receptor that prevents the excess secretion of gastric acid. It is also beneficial for treating peptic, duodenal and gastric ulcers. Some of the common side effects of Lafutidine includes diarrhea, vomiting, nausea, constipation and dizziness and may also cause an increase in liver enzymes and blood urea. It is highly reactive and beneficial for instant results. This drug is not suitable for a person below the age of 18 year and adults can only take it under supervision of doctor.



High Purity and Quality Compliance

Lafutidine is produced to meet or exceed pharmacopoeial and in-house quality standards, delivering a purity of at least 99.0%. Heavy metal content and impurities comply with regulatory norms, making it suitable for reliable pharmaceutical formulations. Its crystalline, odorless, white to off-white appearance attests to its refined manufacturing and stringent quality assurance.


Recommended Handling and Storage Conditions

To maintain Lafutidines stability and effectiveness, it is recommended to store the product at 2-8C in a cool, dry area, protected from direct sunlight. The API remains stable under these conditions, preserving both its potency and a 5-year shelf life. Packing options, including HDPE drums, are chosen to safeguard the product during storage and transportation.


Application and Benefits in Pharmaceutical Industry

Lafutidine serves as an anti-ulcer agent and potent H2 receptor antagonist, widely used in pharmaceutical formulations for gastrointestinal therapy. Its high quality, stability, and reliability ensure consistent results in drug manufacturing, offering therapeutic benefits for patients by reducing stomach acid and promoting ulcer healing.

FAQs of Lafutidine:


Q: How should Lafutidine be stored to ensure maximum stability?

A: Lafutidine should be stored at a temperature between 2-8C in a cool, dry place and kept away from direct sunlight. These conditions are recommended to maintain its stability, purity, and 5-year shelf life.

Q: What is the primary use of Lafutidine in the pharmaceutical industry?

A: Lafutidine is primarily used as an anti-ulcer agent and H2 receptor antagonist in pharmaceutical formulations, helping reduce stomach acid and support ulcer healing.

Q: What are the impurity and heavy metal standards for Lafutidine?

A: Lafutidine complies with pharmacopoeial requirements for impurities and in-house standards. The product has heavy metal content of not more than 0.001%, ensuring it meets high safety and quality criteria.

Q: When and where is the optimal packing option chosen for Lafutidine?

A: Packing options, such as HDPE drums or custom solutions, are provided at the point of manufacturing or distribution, based on customer requirements. This helps protect the API during storage and shipping.

Q: What is the process for ordering Lafutidine as a bulk API material?

A: Lafutidine can be sourced from distributors, exporters, importers, manufacturers, suppliers, or traders in India. Orders are typically supplied in bulk and packed according to specific customer or regulatory requirements.

Q: What are the benefits of using Lafutidine formulated as a bulk pharmaceutical API?

A: Using Lafutidine as a bulk API offers consistent high purity, reliable performance, and compliance with international standards, facilitating efficient drug manufacturing and therapeutic effectiveness.

Price 100 INR/ Kilograms

  • Minimum Order Quantity
  • 1 Kilograms
  • Supply Ability
  • 2000 Kilograms Per Day
  • Delivery Time
  • 1 Days
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"We are into Supply of Pharmaceutical Raw Material / API". We only deal in Bulk Quantity. We do not deals in Pakistan and Bangladesh Countries.