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Available Variants100 g
CHA.79393-100g
Price
€52.48
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
100 g | CHA.79393-100g | €52.48 |
98%
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) | C9H7NO · 0.5H2O4S · 0.5H2O |
|---|---|
| CAS Number | 207386-91-2 |
| Molecular Weight | 203.20 |
| NACRES | NA.22 |
| PubChem Substance ID | 24846798 |
| UNSPSC Code | 12352100 |
| EC Number | 205-137-1 |
| MDL number | MFCD00149610 |
| Assay | 98% |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H302 |
| pcodes | P264 - P270 - P301 + P312 - P501 |
| Hazard Classifications | Acute Tox. 4 Oral |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
8-Hydroxyquinoline hemisulfate salt hemihydrate, with a CAS number of 207386-91-2, is a chemical compound that has garnered significant attention in various scientific fields. This compound is a derivative of 8-hydroxyquinoline, which is a versatile chelating agent known for its ability to form stable complexes with metal ions. The hemisulfate salt hemihydrate form of this compound exhibits enhanced solubility and stability, making it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique properties also render it useful in analytical chemistry, particularly in the detection and quantification of metal ions in environmental and biological samples. As a result, 8-hydroxyquinoline hemisulfate salt hemihydrate is a highly sought-after compound in research and industrial applications, driving ongoing efforts to optimize its synthesis and characterization.
