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VIDAGLIPTIN IP/BP/EP/USP

Name: VIDAGLIPTIN IP/BP/EP/USP
Brand: IPSUM LIFESCIENCES LLP
Price: 1800 INR
Availability: InStock

Price 1800 INR/ Kilograms

Get a Price/Quote

MOQ : 25 Kilograms

VIDAGLIPTIN IP/BP/EP/USP Specification

Molecular Weight
303.4 g/mol

Heavy Metal (%)
NMT 0.001%

Residue on Ignition
NMT 0.1%

Place of Origin
India

Moisture (%)
NMT 0.5%

Loss on Drying
NMT 0.5%

Assay
>99%

Melting Point
158-160 C

HS Code
29420090

Molecular Formula
C17H25N3O2

Storage
Store in a cool, dry place

Particle Size
NMT 100 micron

Other Names
Vildagliptin

CAS No
274901-16-5

Type
Pharmaceutical API

Grade
Pharma Grade

Usage
Used for the treatment of type 2 diabetes mellitus

Purity
>99% (HPLC)

Appearance
White to off-white crystalline powder

Application
Pharmaceuticals

Raw Material
Chemical synthesis

Smell
Odorless

Color
White to off-white

Form
Powder

Shelf Life
3 years under recommended storage

Packaging
HDPE drums or customized according to customer

Identification
Complies with IP/BP/EP/USP specifications

Storage Conditions
Protected from light and moisture

Impurity Profile
Complies with pharmacopeial requirements

Solubility
Freely soluble in water, methanol; sparingly soluble in ethanol

About VIDAGLIPTIN IP/BP/EP/USP

Vildagliptin is an oral medication used to treat type 2 diabetes mellitus. It belongs to the class of dipeptidyl peptidase-4 (DPP-4) inhibitors, which work by increasing insulin secretion and reducing glucose production in the body. This helps to lower blood sugar levels after meals. Vildagliptin is typically taken once or twice daily in tablet form. It appears as a white to slightly yellowish crystalline powder and is soluble in water but less so in ethanol. The medication meets stringent quality standards outlined by pharmacopeias like IP, BP, EP, and USP, ensuring its effectiveness and safety for diabetes management.

High Purity and Compliance

VIDAGLIPTIN adheres to strict international pharmacopeial standards, ensuring an assay and purity greater than 99%. Its impurity profile and safety characteristics, including low moisture, heavy metal, and residue on ignition, confirm its suitability for use in pharmaceutical applications.

Optimal Storage and Longevity

This API is stable for up to three years if stored properly-protected from light and moisture and kept in a cool, dry environment. Adhering to these storage conditions helps preserve product integrity and effectiveness throughout its shelf life.

FAQ's of VIDAGLIPTIN IP/BP/EP/USP:

Q: How should VIDAGLIPTIN IP/BP/EP/USP be stored to ensure maximum shelf life?

A: VIDAGLIPTIN should be stored in a cool, dry place, protected from light and moisture, ideally in its original packaging such as HDPE drums. Proper storage maintains its efficacy for up to three years.

Q: What are the recommended packaging options for VIDAGLIPTIN?

A: VIDAGLIPTIN is typically packed in high-density polyethylene (HDPE) drums but can be customized based on the customer's requirements to suit particular storage and transportation needs.

Q: When is VIDAGLIPTIN used in pharmaceutical manufacturing?

A: VIDAGLIPTIN is employed during the formulation of medications intended for the management of type 2 diabetes mellitus. Its high purity and compliance make it ideal for pharmaceutical preparations.

Q: Where is VIDAGLIPTIN manufactured and supplied from?

A: VIDAGLIPTIN is manufactured, supplied, and traded from India, ensuring adherence to international quality and regulatory standards.

Q: What benefits does VIDAGLIPTIN provide in pharmaceutical applications?

A: VIDAGLIPTIN offers consistent quality, high purity above 99%, and compliance with major pharmacopeias, making it a reliable API for safe and effective diabetes medications.

Q: How is the quality of VIDAGLIPTIN verified?

A: Quality is confirmed through compliance with IP/BP/EP/USP specifications. Stringent tests check its assay, impurity profile, moisture content (NMT 0.5%), and other critical attributes.

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