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Alogliptin(Alogliptine, Alogliptina) CAS NO 850649-61-5


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CAS No.:850649-61-5

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Alogliptin (Alogliptine, Alogliptina) is a potent and selective dipeptidyl peptidase-4 (DPP-4) inhibitor. This compound is a critical active pharmaceutical ingredient (API) used in the management of type 2 diabetes mellitus. It is essential for pharmaceutical manufacturers and research institutions developing innovative antidiabetic therapies. Our supply ensures high purity and consistent quality for reliable formulation and research outcomes.

Application

  • Pharmaceutical API: Primary use as the active ingredient in oral antidiabetic medications for type 2 diabetes.
  • Fixed-Dose Combination Drugs: Used in combination with other antidiabetic agents like metformin or pioglitazone.
  • Pharmaceutical Research & Development: Serves as a key reference standard and building block in metabolic disease research.
  • Formulation Development: Utilized in the development and testing of various dosage forms, including tablets.
  • Analytical Standard: Acts as a high-purity standard for quality control and analytical method development (HPLC, LC-MS).
  • Clinical Trial Material: Supplied as a GMP-grade material for pre-clinical and clinical studies.

Basic Information

Product Name Alogliptin (Alogliptine, Alogliptina)
CAS No. 850649-61-5
Molecular Formula C18H21N5O2
Molecular Weight 339.40 g/mol
Synonyms Alogliptin; Alogliptine; Alogliptina; SYR-322; 2-({6-[(3R)-3-Aminopiperidin-1-yl]-3-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl}methyl)benzonitrile; Nesina (Brand Name); (R)-2-((6-(3-Aminopiperidin-1-yl)-3-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)methyl)benzonitrile
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Quality Control

Our Alogliptin is manufactured and tested under strict quality systems. We provide material that meets or exceeds pharmaceutical-grade standards, with typical purity levels >98.5% (HPLC). Each batch is supported by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We adhere to ICH Q7 guidelines and can supply material suitable for GMP applications upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept under dry, inert conditions to maintain stability and potency.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference standard
Identification (HPLC) Retention time matches reference
Assay (HPLC) ≥ 98.5%
Related Substances (HPLC) Total impurities ≤ 1.0% Any single unknown impurity ≤ 0.10%
Residual Solvents (GC) Complies with ICH Q3C
Water Content (KF) ≤ 0.5%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

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Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.