Ordering
Available Variants5 g
CHA.49734-5g
Price
€30.32
Available – Dispatch in 14 days
25 g
CHA.49734-25g
Price
€98.40
Available – Dispatch in 14 days
100 g
CHA.49734-100g
Price
€342.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.49734-5g | €30.32 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.49734-25g | €98.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
100 g | CHA.49734-100g | €342.40 |
suitable for fluorescence, anhydrous, ≥98.0% (dried material, NT)
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) | C20H24N2O2 |
|---|---|
| CAS Number | 130-95-0 |
| Molecular Weight | 324.42 |
| UNSPSC Code | 12171500 |
| NACRES | NA.32 |
| PubChem Substance ID | 57647993 |
| EC Number | 205-003-2 |
| Beilstein/REAXYS Number | 91867 |
| MDL number | MFCD00198096 |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H302,H317 |
| pcodes | P261 - P264 - P272 - P280 - P301 + P312 - P302 + P352 |
| Hazard Classifications | Acute Tox. 4 Oral - Skin Sens. 1 |
| Storage Class | 11 - Combustible Solids |
| ppe | dust mask type N95 (US), Eyeshields, Faceshields, Gloves |
Technical Overview & Applications Use-case context
Quinine, with the chemical formula C20H24N2O2 and CAS number 130-95-0, is a naturally occurring alkaloid compound derived from the bark of the cinchona tree. It has been widely used for centuries in the treatment and prevention of malaria, due to its ability to interfere with the replication of the Plasmodium parasite. Quinine functions by inhibiting the parasites ability to break down hemoglobin, thereby preventing the parasite from obtaining the necessary nutrients for survival. The compound has also been used to treat other conditions, such as babesiosis and amoebiasis, although its use has been largely supplanted by more modern and effective treatments. Despite this, quinine remains an important compound in the field of pharmacology and continues to be studied for its potential therapeutic applications, particularly in the development of new antimalarial agents. Its mechanism of action is still not fully understood.
