Ordering
Available Variants5 mg
CHA.94213-5mg
Price
€111.20
Available – Dispatch in 14 days
25 mg
CHA.94213-25mg
Price
€427.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 mg | CHA.94213-5mg | €111.20 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 mg | CHA.94213-25mg | €427.20 |
≥98% (HPLC), α-glucosidase inhibitor, powder
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) | C16H12 O6 |
|---|---|
| CAS Number | 1447-88-7 |
| Molecular Weight | 300.26 |
| NACRES | NA.77 |
| UNSPSC Code | 12352200 |
| MDL number | MFCD00143504 |
| 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
Hispidulin, with the chemical formula C16H12O6 and CAS number 1447-88-7, is a naturally occurring flavonoid compound found in various plant species. It is characterized by its distinct chemical structure, which consists of a flavone backbone with specific hydroxyl and methoxyl substituents. Hispidulin has been reported to exhibit a range of biological activities, including antioxidant, anti-inflammatory, and antimicrobial properties, making it a compound of interest for potential therapeutic applications. The compound has been isolated from several plant sources, including species of the genera Teucrium and Scutellaria, and its chemical synthesis has also been achieved through various methods. Further research is needed to fully elucidate the pharmacological properties and potential uses of hispidulin, but its unique chemical structure and biological activities make it a promising area of study.
