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Linagliptin Structure

Product Type

Active Pharmaceutical Ingredient (API)

Grade

USP / BP / EP (as applicable)

Chemical Name

Linagliptin

Chemical Formula

C₂₅H₂₈N₈O₂

Molecular Weight

~472.55 g/mol

CAS Number

668270-12-0

IUPAC Name

8-[(3R)-3-aminopiperidin-1-yl]-7-(but-2-yn-1-yl)-3-methyl-1-[(4-methylquinazolin-2-yl)methyl]-3,7-dihydro-1H-purine-2,6-dione

Chemical Class

Xanthine derivative

Therapeutic Class

Antidiabetic

Synonyms

PHYSIOCHEMICAL PROPERTIES

Appearance White to off-white crystalline powder
Solubility Practically insoluble in water; soluble in DMSO, methanol, and ethanol
Melting Point 295–298°C
pH -

Product Description

Linagliptin is an oral antidiabetic agent that selectively inhibits dipeptidyl peptidase-4 (DPP-4), an enzyme responsible for the breakdown of incretin hormones like GLP-1. By prolonging incretin activity, it enhances glucose-dependent insulin secretion and suppresses glucagon release, helping to maintain blood glucose levels in patients with type 2 diabetes mellitus. Linagliptin offers the advantage of once-daily dosing without dose adjustment in mild-to-moderate renal impairment.

How Linagliptin Works

Linagliptin selectively inhibits DPP-4, preventing the degradation of incretin hormones such as GLP-1 and GIP. This action enhances glucose-dependent insulin secretion from pancreatic β-cells and suppresses glucagon secretion, thereby reducing hepatic glucose production. When used as monotherapy, it does not cause significant hypoglycemia, making it a safe and effective option for managing type 2 diabetes.

Use(s)

Adverse Effects

Why choose Salius for Linagliptin?

  1. Regulatory-Grade Manufacturing Standards
    They maintain WHO GMP compliance, with some facilities FDA certified, and follow stringent internal QC protocols. Every batch is tested in state-of-the-art labs before release.
  2. Enhancing Cost-Effectiveness Through Large Volume API Utilization
    As an exporter and distributor house, Salius aims to deliver high-quality APIs at competitive prices, a key advantage for cost-sensitive markets.
  3. Global Export Experience & Documentation Support
    Salius regularly exports APIs, provides regulatory documents (DMF, impurity profiles), and supports filings for international clients—even in stringent regulated markets.
  4. Documents We Provide
  5. Transparency & Trustworthiness
    They present as a government-recognized star export house with strong quality and delivery ratings.
Attribute Why Salius Pharma Is a Good Choice
Quality Certification WHO GMP, ISO 9001:2015, FDA audited facilities
Affordability & Generic Access Cost competitive generics for global supply
Export Experience Proven track record of supplying globally

What You Receive in Our Package

When you order from Salius Pharma, you receive more than just a product — you receive a complete, professionally prepared package that meets international regulatory and quality expectations.

Each Shipment Includes:

Product

Expected Delivery Time

We ensure prompt and reliable shipping worldwide. Delivery times vary depending on destination, order volume, and regulatory requirements.

Overall Delivery Time:

7 to 21 business days from dispatch, depending on your location.

FAQs

Yes, widely used in tablets and fixed-dose combinations for type 2 diabetes.

Yes, all documentation is supplied for export and regulated markets.

Yes, fully cGMP-compliant with validated QC methods.

Yes, custom particle sizes and grades are available to optimize dissolution and formulation.

Yes, long-term and accelerated stability studies confirm API stability for tropical and temperate climates.

Place an Order or Request a Quote from Salius Pharma

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Whether you need Active Pharmaceutical Ingredients (APIs), finished formulations, or regulatory support, our team is ready to provide dependable, compliant, and cost-effective solutions tailored to your market needs.

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