DIMETHISOQUIN HYDROCHLORIDE (2 G)
- Product Name
- DIMETHISOQUIN HYDROCHLORIDE (2 G)
- CAS No.
- 2773-92-4
- Chemical Name
- DIMETHISOQUIN HYDROCHLORIDE (2 G)
- Synonyms
- quotane;QuinisocaineHCl;chinisocainehydrochloride;quinisocainehydrochloride;dimethisoquinhydrochloride;DIMETHISOQUIN HYDROCHLORIDE (2 G);Dimethisoquin Hydrochloride (1208001);3-butyl-1-(2-(dimethylamino)ethoxy)-isoquinolinhydrochloride;3-butyl-1-(2-(dimethylamino)ethoxy)isoquinolinehydrochloride;2-[(3-butyl-1-isoquinolyl)oxy]ethyl(dimethyl)ammonium chloride
- CBNumber
- CB6505774
- Molecular Formula
- C17H25ClN2O
- Formula Weight
- 308.8462
- MOL File
- 2773-92-4.mol
DIMETHISOQUIN HYDROCHLORIDE (2 G) Property
- Melting point:
- 145.5°C
- Density
- 1.0887 (rough estimate)
- refractive index
- 1.5800 (estimate)
- storage temp.
- Hygroscopic, Refrigerator, under inert atmosphere
- solubility
- DMSO (Slightly, Heated), Methanol (Slightly)
- form
- Solid
- color
- White to Off-White
- Stability:
- Hygroscopic
Safety
- Toxicity
- LD50 i.p. in rats: 45-50 mg/kg (Fellows, Macko)
N-Bromosuccinimide Price
- Product number
- D460475
- Product name
- DimethisoquinHydrochloride
- Packaging
- 25mg
- Price
- $275
- Updated
- 2021/12/16
DIMETHISOQUIN HYDROCHLORIDE (2 G) Chemical Properties,Usage,Production
Originator
Quotane,SKF,US,1951
Uses
Dimethisoquin Hydrochloride is a local anesthetic.
Definition
An ointment and lotion containing dimethisoquin hydrochloride.
Manufacturing Process
A mixture of 10.0 grams of β-dimethylaminoethanol and 1.9 grams of sodium in 90 cc of dry xylene was heated at 95°C for 5 hours. To the resulting solution was added at 30°C, 18 grams of 3-butyl-1-chloroisoquinoline. The solution, which turned very dark, was heated at 100°-125°C for 3.5 hours. The mixture was extracted with two 100 cc portions of 2N hydrochloric acid solution. The acid solution was made strongly alkaline with 40% potassium hydroxide solution and the oil which separated was taken into ether. The ether solution was washed with two 100 cc portions of water saturated with sodium chloride, and then dried over anhydrous sodium sulfate for 3 hours. The sodium sulfate was removed by filtration and the ether by distillation. Distillation of the residual oil gave a colorless liquid, BP 155°-157°C/3mm.
Therapeutic Function
Local anesthetic