Description

Indinavir (100 Mg)F0D3080.971Mg/Mg(Ai) is a high-purity active pharmaceutical ingredient (API) and a potent, selective inhibitor of the HIV-1 protease enzyme. This compound is critical for the formulation of antiretroviral medications used in the management of HIV infection. It is essential for pharmaceutical manufacturers and research institutions engaged in the development and production of antiviral therapies, particularly for combination antiretroviral treatment (cART) regimens.

Application

• Pharmaceutical API: Primary active ingredient in the formulation of antiretroviral drugs for the treatment of HIV-1 infection.
• Combination Therapy: Used in fixed-dose combination tablets as part of highly active antiretroviral therapy (HAART).
• Research & Development: Key reference standard and intermediate in virology research, drug discovery, and mechanism of action studies.
• Generic Drug Manufacturing: Serves as the core API for the production of generic versions of protease inhibitor medications.
• Clinical Trial Materials: Used in the preparation of investigational new drugs (INDs) for clinical studies.
• Analytical Standard: High-purity grade suitable for use as a calibration standard in HPLC, LC-MS, and other analytical methods for quality control.

Basic Information

Product Name	Indinavir (100 Mg)F0D3080.971Mg/Mg(Ai)
CAS No.	180683-37-8
Molecular Formula	C36H47N5O4
Molecular Weight	613.80 g/mol
Synonyms	Indinavir; Indinavir Sulfate; MK-639; L-735,524; Crixivan® (brand name); (2S)-1-[(2S,4R)-4-Benzyl-2-hydroxy-4-[[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]carbamoyl]butyl]-N-tert-butyl-4-(pyridin-3-ylmethyl)piperazine-2-carboxamide; HIV-1 Protease Inhibitor
EINECS	Contact for details

Quality Control

Our Indinavir is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent pharmaceutical-grade specifications, including identity, purity, and impurity profile. Certificates of Analysis (COA) documenting compliance with relevant pharmacopeial standards (such as USP/EP) are provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to maintain stability and potency. For long-term storage, consider desiccated conditions.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Specific Optical Rotation	Contact for details

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