Demecariumbromid

Bezeichnung:Demecariumbromid

CAS-Nr56-94-0

Englisch Name:Demecarium bromide

CBNumberCB6501408

SummenformelC32H52Br2N4O4

Molgewicht716.59

MOL-Datei56-94-0.mol

Synonyma

Demecariumbromid

Demecariumbromid physikalisch-chemischer Eigenschaften

Schmelzpunkt	162-167 °C (decomp)
storage temp.	Store at -20°C
Löslichkeit	DMSO:160.0(Max Conc. mg/mL);223.28(Max Conc. mM)
Aggregatzustand	Solid
Farbe	White
InChIKey	YHKBUDZECQDYBR-UHFFFAOYSA-L
SMILES	C1(=CC=CC([N+](C)(C)C)=C1)OC(=O)N(C)CCCCCCCCCCN(C)C(=O)OC1=CC=CC([N+](C)(C)C)=C1.[Br-].[Br-]
CAS Datenbank	56-94-0(CAS DataBase Reference)

Sicherheit

HS Code	2924296000
Giftige Stoffe Daten	56-94-0(Hazardous Substances Data)

Gefahreninformationscode (GHS)

Demecarium bromide Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften
White Solid
Originator
Humorsol ,MSD ,US,1959
Verwenden
Demecarium is a disymmetrical compound that contains two ammonium and two carbamate groups. It is a reversible cholinesterase inhibitor that is longer lasting than the others. It is used to constrict pupils, elevate intraocular pressure in treating glaucoma, and also for alleviating atropine mydriasis.
Verwenden
anticancer agent for pancreatic islet cells
Verwenden
Demecarium Bromide is an acetylcholinesterase inhibitor and veterinary medicine used to treat elevated intraocular pressure associated with primary glaucoma.
Definition
ChEBI: The methobromide salt of the N,N'-bis[3-(dimethylamino)phenyl carbamate] derivative of 2,13-diazatetradecane. It is an inhibitor of acetylcholinesterase and pseudocholinesterase, with a long duration of action. It is u ed in the treatment of chronic open-angle glaucoma: in the eye, it causes constriction of the iris sphincter muscle and the ciliary muscle, facilitating the outflow of the aqueous humor and so reducing intraocular pressure.
Manufacturing Process
N,N,N,N'-tetramethyldecamethylene diamine is reacted with phosgene in toluene under agitation. The phosgene which escapes through an ascending cooling tube together with the evolved methyl chloride is condensed in a cold trap. As soon as immixture has been completed, the temperature is raised to 100°C and the phosgene recovered in the trap is vaporized and bubbled through the solution again, the escaping gas being recondensed and returned once more. The repeated passage through the reagents of the phosgene that has not yet reacted is continued for 7 hours. When the solution is cool it is passed through a filter, the remaining phosgene is removed from the clear solution by distillation and the remainder distilled in vacuo.
A solution of 11.9 parts of m-dimethylaminophenol in 90 parts of xylene (isomer mixture) is added to a solution of sodium methylate consisting of 2.0 parts of sodium and 25 parts of methanol. The methanol is then completely removed by distillation and the temperature raised until the boiling point of the xylene is reached. The decamethylene-bis-(N-methyl carbamic chloride) is added to the remainder which contains the sodium salt of m dimethylaminophenol in the form of solid crystals. The reagent mixture is heated and maintained at a temperature of 100°C and continuously agitated. After having been cooled it is washed three times in water, three times in a 5% solution of caustic soda, and another three times in water. The xylene is then evaporated in vacuo and the oily residue freed of any remaining traces of xylene by allowing it to stand in air when the product crystallized completely. In this manner 15.6 parts of decamethylene-bis-(N-methyl carbamic acid mdimethylaminophenylester) are obtained, This is in turn reacted with methyl bromide to give the desired product. The decamethylene-bis-(N-methyl carbamic acid m-dimethylaminophenylesterbromomethylate) appears after precipitation from a solution in acetic acid with methyl ethyl ketone in the form of a finely crystalline powder with a micro melting point between 164° and 170°C.
Trademarks
Humorsol (Merck).
Therapeutic Function
Cholinergic (ophthalmic)
Allgemeine Beschreibung
Demecarium bromide,(m-hydroxyphenyl)trimethylammonium bromide, decamethylenebis[methylcarbamate] (Humorsol), is the diester of(m-hydroxyphenyl)trimethylammonium bromide with decamethylene-bis-(methylcarbamic acid) and thus is comparableto a bis-prostigmine molecule.
It occurs as a slightly hygroscopic powder that is freelysoluble in water or alcohol. Ophthalmic solutions of the drughave a pH of 5 to 7.5. Aqueous solutions are stable and maybe sterilized by heat. Its efficacy and toxicity are comparableto those of other potent anticholinesterase inhibitor drugs. Itis a long-acting miotic used to treat wide-angle glaucomaand accommodative esotropia. Maximal effect occurs hoursafter administration, and the effect may persist for days.
Synthese
Demecarium, N,N??-decamethylene-bis-[meta-(N-methylcarbamoyloxy)- phenyl-trimethylammonium] hydroxide (13.2.18), is made by reacting two moles of phosgene with 1,10-bis-(methylamino)-decano(N,N??-dimethyldecamethylen-1,10-diamine, giving the bis-carbamoylchloride (13.2.16), which is transformed into bis-carbamoylester (13.2.17) by reaction with two moles of the 3-dimethylaminophenol sodium salt. Reacting this with methylbromide gives demecarium (13.2.18) [49].
Veterinary Drugs and Treatments
Demecarium is a potent carbamate inhibitor that may reduce intraocular pressures for up to 48 hours in canines. Demecarium reversibly inhibits anticholinesterase thereby causing miosis. Demecarium is generally used in preventive management of the contralateral eye in canine patients after the diagnosis of an acute congestive crisis of primary glaucoma in the other eye. It is not used in secondary glaucoma. Demecarium has the advantage of once or twice daily dosing.

Demecarium bromide Upstream-Materialien And Downstream Produkte

Demecariumbromid Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

56-94-0, Demecarium bromide Verwandte Suche:

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