Ordering
Available Variants10 mg
CHA.51083-10mg
Price
€107.20
Available – Dispatch in 14 days
50 mg
CHA.51083-50mg
Price
€393.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
10 mg | CHA.51083-10mg | €107.20 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
50 mg | CHA.51083-50mg | €393.60 |
≥98% (HPLC), powder, antiretroviral agent
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C36H47N5O4·H2SO4 · xH2O |
|---|---|
| Molecular Weight | 711.87 (anhydrous basis) |
| UNSPSC Code | 51111800 |
| NACRES | NA.77 |
| Assay | ≥98% (HPLC) |
| Form | powder |
| Quality level | 100 |
| Storage condition | desiccated |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
Indinavir sulfate salt hydrate, with a CAS number of 157810-81-6, is a crystalline solid that serves as a key intermediate in the synthesis of indinavir, a potent inhibitor of the human immunodeficiency virus (HIV) protease. The compound is highly soluble in water and exhibits a high degree of stability under various storage conditions. As a sulfate salt hydrate, it is commonly utilized in the production of indinavir, which is administered orally for the treatment of HIV infection. The synthesis of indinavir sulfate salt hydrate involves a multi-step process, including the reaction of indinavir with sulfuric acid, followed by crystallization and purification. The resulting compound is then subjected to rigorous quality control measures to ensure its purity and suitability for use in pharmaceutical applications. Its importance lies in its role as a precursor to indinavir, a crucial component of HIV therapy regimens.
