Quinine
ALDRICH/145904 - 90%
Synonym: 6′-Methoxycinchonidine
CAS Number: 130-95-0
Empirical Formula (Hill Notation): C20H24N2O2
Molecular Weight: 324.42
EC Number: 205-003-2
MDL Number: MFCD00198096
Linear Formula: C20H24N2O2
Product Type: Chemical
| assay | 90% |
| functional group | hydroxyl |
| InChI | 1S/C20H24N2O2/c1-3-13-12- |
| InChI key | LOUPRKONTZGTKE-WZBLMQSHSA |
| mp | 173-175 °C (lit.) |
| optical activity | [α]25/D −165°, c = 2 in ethanol |
| Quality Level | 200 ![]() |
| SMILES string | COc1ccc2nccc([C@@H](O)[C@ |
| Application: | Quinine has been used as a standard during the chemical evaluation of alkaloids in the hydroethanolic extracts of endophytic fungi obtained from the leaves of Costus spiralis by TLC. |
| Application: | Resolving agent for carboxylic acids. Catalyzes the kinetic resolution of furanones. |
| Biochem/physiol Actions: | Potassium channel blocker |
| General description: | Quinine, a cinchona alkaloid found in the bark of the cinchona tree, is known for its anti-malarial property. |
| Other Notes: | remainder hydroquinine |
| Packaging: | 10, 50 g in poly bottle |
| Symbol | GHS07 |
| Signal word | Warning |
| Hazard statements | H302 - H317 |
| Precautionary statements | P261 - P264 - P280 - P301 + P312 + P330 - P302 + P352 - P333 + P313 |
| Hazard Codes | Xn |
| Risk Statements | 36/38-42/43 |
| Safety Statements | 22-26-36/37-45 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 1 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Purity | 90% |
| mp | 173-175 °C (lit.) |
| UNSPSC | 12352104 |


