A5454812
Moclobemide (Ro 111163) , 98% , 71320-77-9
Synonym(s):
4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide;Aurorix;Moclamine
CAS NO.:71320-77-9
Empirical Formula: C13H17ClN2O2
Molecular Weight: 268.74
MDL number: MFCD00865388
EINECS: 629-727-7
| Pack Size | Price | Stock | Quantity |
| 10MG | RMB228.80 | In Stock |
|
| 50MG | RMB905.60 | In Stock |
|
| 100mg | RMB1574.40 | In Stock |
|
| 250MG | RMB3039.20 | In Stock |
|
| others | Enquire |
Update time: 2022-07-08
PRODUCT Properties
| Melting point: | 137°C |
| Boiling point: | 447.7±40.0 °C(Predicted) |
| Density | 1.206±0.06 g/cm3(Predicted) |
| storage temp. | room temp |
| solubility | DMSO: >20mg/mL |
| pka | 14.26±0.46(Predicted) |
| form | solid |
| color | white |
| Merck | 14,6226 |
| InChI | InChI=1S/C13H17ClN2O2/c14-12-3-1-11(2-4-12)13(17)15-5-6-16-7-9-18-10-8-16/h1-4H,5-10H2,(H,15,17) |
| InChIKey | YHXISWVBGDMDLQ-UHFFFAOYSA-N |
| SMILES | C(NCCN1CCOCC1)(=O)C1=CC=C(Cl)C=C1 |
| CAS DataBase Reference | 71320-77-9(CAS DataBase Reference) |
| NIST Chemistry Reference | Moclobemide(71320-77-9) |
Description and Uses
Moclobemide is the first of a new generation of non-hydrazine, reversible MAO-A inhibitors useful in the treatment of depression. Moclobemide is a selective inhibitor of MAO-A, allowing tyramine to be metabolized by MAO-B. In controlled studies, moclobemide was clinically superior to desipramine and showed no cholinergic or cardiovascular side-effects. A metabolite is currently under investigation for treatment of Parkinson’s disease,.
A reversible monoamine oxidase inhibitor.
Safety
| Symbol(GHS) | ![]() ![]() GHS05,GHS07 |
| Signal word | Danger |
| Hazard statements | H302-H315-H318-H335 |
| Precautionary statements | P280-P301+P312+P330-P302+P352-P305+P351+P338+P310 |
| Hazard Codes | Xn,T+ |
| Risk Statements | 22-37/38-41-26/27/28 |
| Safety Statements | 26-39-45-36/37/39-22 |
| RIDADR | 3249 |
| WGK Germany | 2 |
| RTECS | CV2462000 |
| HazardClass | 6.1(b) |
| PackingGroup | III |
| HS Code | 29349990 |
| Hazardous Substances Data | 71320-77-9(Hazardous Substances Data) |
| Toxicity | LD50 in rats (mg/kg): 707 orally (Burkard, Wyss) |








