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Glimepiride Api Powder
Glimepiride Api Powder

Glimepiride Api Powder

Price 28600.0 INR/ Piece

MOQ : 10 Pieces

Glimepiride Api Powder Specification

  • Solubility
  • Practically insoluble in water; soluble in methanol, slightly soluble in ethanol
  • Poisonous
  • No (When used as specified)
  • Structural Formula
  • C24H34N4O5S
  • Heavy Metal (%)
  • 0.001%
  • HS Code
  • 29420090
  • Taste
  • Tasteless
  • Storage
  • Store in a tightly closed container, protected from light, moisture, and excessive heat
  • Boiling point
  • Not available (decomposes)
  • Shelf Life
  • 3 years from manufacturing date
  • Molecular Weight
  • 490.62 g/mol
  • Molecular Formula
  • C24H34N4O5S
  • Color
  • White to off-white
  • Smell
  • Odorless
  • Particle Size
  • D90 < 25 microns
  • Ph Level
  • 4.5 6.5 (1% solution)
  • Loss on Drying
  • 0.5%
  • Melting Point
  • 207-209C
  • EINECS No
  • 405-769-7
  • Medicine Name
  • Glimepiride Api Powder
  • Chemical Name
  • Glimepiride
  • CAS No
  • 93479-97-1
  • Type
  • API (Active Pharmaceutical Ingredient)
  • Grade
  • Pharmaceutical Grade
  • Usage
  • Used as an antidiabetic agent in the treatment of type 2 diabetes mellitus
  • Purity(%)
  • >99%
  • Appearance
  • White to off-white crystalline powder
  • Physical Form
  • Powder
  • Specific Optical Rotation
  • +125 to +135 (c=0.5 in DMF)
  • Identification
  • Complies to standard USP/BP requirements
  • Packing
  • Packed in double LDPE bags inside HDPE drums
  • Related Substances
  • Maximum single impurity: 0.1%, Total impurities: 0.3%
  • Manufacturing Standard
  • Manufactured under GMP compliance
  • Microbial Limit
  • Total aerobic microbial count: 100 CFU/g; Total yeast & mould count: 50 CFU/g
  • Residue on Ignition
  • 0.1%
 

Glimepiride Api Powder Trade Information

  • Minimum Order Quantity
  • 10 Pieces
  • Supply Ability
  • 100 Pieces Per Day
  • Delivery Time
  • 7 Days
  • Sample Available
  • No
  • Sample Policy
  • Contact us for information regarding our sample policy
 

About Glimepiride Api Powder

Product Specification

CAS Number 93479-97-1
Formula: C24H34N4O5S C24H34N4O5S
Purity 99 %
Treatment Treat high blood sugar levels caused by type 2 diabetes
GRADE IP/BP/USP
Minimum Order Quantity 20 Kg

Product Description

packing type

drum
Product DescriptionGlimepirideiis an orally available medium-to-long acting sulfonylurea antidiabetic drug. Glimepiride is indicated to treat type 2 diabetes mellitus; its mode of action is to increase insulin production by the pancreas. Its use is contraindicated in patients with hypersensitivity to glimepiride or other sulfonylureas.

It lowers blood sugar by stimulating the release of insulin by pancreatic beta cells and by inducing increased activity of intracellular insulin receptors.Exports To:iGeorgia | Palestinian National Authority | Latvia | Japan | Iraq

Additional Information

Delivery Time week
Production Capacity 2500
Packaging Details 1kg to 25 kg


Exceptional Purity and Quality Assurance

Glimepiride API Powder offers a purity greater than 99%, meeting rigorous USP/BP standards for pharmaceuticals. With strictly limited impurities and tight microbial controls, it ensures a safe and reliable product suitable for critical pharmaceutical formulation. Regular quality reviews and adherence to GMP guidelines underpin its consistent performance.


Efficiently Packed and Safe for Global Shipment

Our Glimepiride API Powder is carefully packed in double-layer LDPE bags fitted inside robust HDPE drums. This protective packaging maintains the product's stability by shielding it from moisture, light, and contamination, ensuring it arrives safely and intact for use by global suppliers, manufacturers, and importers.


Optimized for Specialized Pharmaceutical Use

Designed specifically for pharmaceutical manufacturing, Glimepiride API Powder is mainly used as an active antidiabetic ingredient. Its precise particle size and dependable chemical properties streamline production processes and enhance medication quality for patients managing type 2 diabetes.

FAQ's of Glimepiride Api Powder:


Q: How is the purity and quality of Glimepiride API Powder ensured?

A: Glimepiride API Powder is manufactured under stringent GMP (Good Manufacturing Practice) compliance, with purity exceeding 99%. The product conforms to USP/BP standards, with single and total impurities kept below 0.1% and 0.3%, respectively, and undergoes thorough quality testing for microbial limits and other key parameters.

Q: What is the recommended process for storing Glimepiride API Powder?

A: To maintain its stability, Glimepiride API Powder should be stored in a tightly closed container, away from light, moisture, and excessive heat. The original double LDPE bags inside HDPE drums provide optimal protection during storage.

Q: When should Glimepiride API Powder be used in pharmaceutical production?

A: Glimepiride API Powder is suitable for use in the formulation of antidiabetic medications at any production phase where the incorporation of an active pharmaceutical ingredient (API) is required. It is typically integrated during the active ingredient blending process of oral antidiabetic drug manufacturing.

Q: Where is the Glimepiride API Powder manufactured and supplied from?

A: Our Glimepiride API Powder is produced in India by GMP-certified facilities and is available for export, import, and local supply. The secure packaging facilitates safe transport to both domestic and international pharmaceutical manufacturers.

Q: What are the key benefits of using Glimepiride API Powder in drug formulations?

A: The high purity, low impurity profile, and strict microbial limits of Glimepiride API Powder ensure the safety and effectiveness of the final medication. Its consistent quality and compliance with pharmacopoeial standards make it an ideal choice for producing safe treatments for type 2 diabetes mellitus.

Q: How is the physical integrity of the powder ensured during shipping?

A: Glimepiride API Powder is packed in double LDPE bags, sealed within HDPE drums, which protect it from contamination, environmental factors, and damage during transit, ensuring the product maintains its quality upon delivery.

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