caramiphen hydrogen edisilate
- Product Name
- caramiphen hydrogen edisilate
- CAS No.
- 125-86-0
- Chemical Name
- caramiphen hydrogen edisilate
- Synonyms
- Ethanedisulfonate;BANIDACEBXZGNK-UHFFFAOYSA-N;Caramiphen ethanedisulfonate;caramiphen hydrogen edisilate;2-diethylaminoethyl 2-phenylcyclopentane-1-carboxylate;2-phenylcyclopentanecarboxylic acid 2-diethylaminoethyl ester;Bis[1-(carbo-β-diethylaminoethoxy)-1-phenylcyclopentane]ethanedisulfonate
- CBNumber
- CB1877872
- Molecular Formula
- 2C18H27NO2.C2H6O6S2
- Formula Weight
- 769.028
- MOL File
- 125-86-0.mol
caramiphen hydrogen edisilate Property
- Melting point:
- 115-116°
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P330Rinse mouth.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- B416465
- Product name
- Bis[1-(carbo-β-diethylaminoethoxy)-1-phenylcyclopentane]ethanedisulfonate
- Packaging
- 500mg
- Price
- $90
- Updated
- 2021/12/16
caramiphen hydrogen edisilate Chemical Properties,Usage,Production
Originator
Panparnit,Geigy,US,1949
Uses
Bis[1-(carbo-β-diethylaminoethoxy)-1-phenylcyclopentane]ethanedisulfonate is an anticholinergic and antiglutamatergic drug, which has also found use as an antidote against oragnophosphate poisoning.
Manufacturing Process
20.8 parts of 1-phenylcyclopentyl-1-carboxylic acid chloride, obtained from
the acid (cf. Am. Soc. 1934, 56, 715) by means of thionyl chloride, are
dissolved in 250 parts by volume of absolute ether, then, while stirring and
cooling with a mixture of common salt and ice a solution of 12 parts of
diethylaminoethanol in 50 parts by volume of absolute ether is allowed to
drop there into, the temperature being maintained below 0°C, whereupon
stirring is continued during 2 hours at room temperature. The whole is then
twice shaken out with water and once with diluted hydrochloric acid, the
combined aqueous solutions are made alkaline with a potassium carbonate
solution and shaken out with ether. The ethereal solution is washed with
water, dried over potassium carbonate and the solvent is distilled off. The base
boils at a pressure of 0.07 mm at 112°C to 115°C.
The base may then be converted to the hydrochloride or to the
ethanedisulfonic acid salt (edisylate).
Therapeutic Function
Antitussive
caramiphen hydrogen edisilate Preparation Products And Raw materials
Raw materials
Preparation Products
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