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| | Flunarizine dihydrochloride Basic information |
| | Flunarizine dihydrochloride Chemical Properties |
| Melting point | 188-190C | | storage temp. | 2-8°C | | solubility | chloroform/methanol (9:1): 50 mg/mL, clear, colorless | | form | Solid | | color | White to Off-White | | Merck | 13,4170 | | BRN | 4284243 | | InChI | InChI=1S/C26H26F2N2.2ClH/c27-24-12-8-22(9-13-24)26(23-10-14-25(28)15-11-23)30-19-17-29(18-20-30)16-4-7-21-5-2-1-3-6-21;;/h1-15,26H,16-20H2;2*1H/b7-4+;; | | InChIKey | RXKMOPXNWTYEHI-RDRKJGRWSA-N | | SMILES | C(C1C=CC(F)=CC=1)(C1=CC=C(F)C=C1)N1CCN(C/C=C/C2C=CC=CC=2)CC1.Cl.Cl | | CAS DataBase Reference | 30484-77-6(CAS DataBase Reference) |
| Hazard Codes | Xn | | Risk Statements | 22 | | WGK Germany | 3 | | RTECS | TK9187000 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral |
| | Flunarizine dihydrochloride Usage And Synthesis |
| Chemical Properties | White Solid | | Originator | Sibelium,Janssen,W. Germany,1977 | | Uses | Flunarizine dihydrochloride has been used to study the effect of flunarizine on epileptiform activity. It is also used to study its effect on high-potassium induced increase of intracellular free calcium. | | Uses | antipsychotic, H1 antihistamine | | Uses | Calcium channel blocker; fluorinated derivative of Cinnarizine. Vasodilator (cerebral and peripheral). This is the labeled analog. | | Definition | ChEBI: Flunarizine hydrochloride is a diarylmethane. | | Manufacturing Process | A mixture of 14.3 parts of di-(p-fluorophenyl)-chloromethane, 10.1 parts of 1-
cinnamylpiperazine, 12.7 parts of sodium carbonate, a few crystals of
potassium iodide in 200 parts of 4-methyl-2-pentanone is stirred and refluxed
for 21 hours. The reaction mixture is cooled and 50 parts of water are added.
The organic layer is separated, dried, filtered and evaporated.
The oily residue is dissolved in 480 parts of anhydrous diisopropyl ether. This
solution is boiled with activated charcoal, filtered and to the clear filtrate is
added an excess of 2-propanol, previously saturated with gaseous hydrogen
chloride. The precipitated salt is filtered off and recrystallized from a mixture
of 2-propanol and ethanol, yielding 1-cinnamyl-4-(di-p-fluorobenzhydryl)
piperazine dihydrochloride, MP 251.5°C. | | Therapeutic Function | Vasodilator | | General Description | Flunarizine has antihistamine, anticonvulsant and vestibular depressive properties. It protects endothelial cells from calcium overload-induced damage. Flunarizine is used to treat epilepsy, migraine prophylaxis, cerebral blood flow disturbances, peripheral vascular disease and vertigo. | | Biological Activity | Dual Na + /Ca 2+ channel blocker; a cerebral and peripheral vasodilator. Neuroprotective. | | Biochem/physiol Actions | Blocks T-type Ca2+/Na+ channels; inhibits K+-induced catecholamine release from chromaffin cells |
| | Flunarizine dihydrochloride Preparation Products And Raw materials |
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