Oxymetazoline

Oxymetazoline
  • CAS No.:1491-59-4
Other grades of this product :
Oxymetazoline Basic information
Product Name:Oxymetazoline
Synonyms:afrin;h990;H-990;Hazol;Iliadin;Nafrine;nasivin;Nasivine
CAS:1491-59-4
MF:C16H24N2O
MW:260.37
EINECS:216-079-1
Product Categories:Pharmaceuticals;Aromatics;Heterocycles;Intermediates & Fine Chemicals
Mol File:1491-59-4.mol
Oxymetazoline Chemical Properties
Melting point 182 °C
Boiling point 403.63°C (rough estimate)
density 0.9822 (rough estimate)
refractive index 1.5800 (estimate)
pka11.93±0.28(Predicted)
color Crystals from C6H6
CAS DataBase Reference1491-59-4(CAS DataBase Reference)
NIST Chemistry ReferenceOxymetazoline(1491-59-4)
Safety Information
RIDADR 3249
HazardClass 6.1(a)
PackingGroup II
Hazardous Substances Data1491-59-4(Hazardous Substances Data)
ToxicityLD50 orl-rat: 800 mg/kg TXAPA9 18,185,71
MSDS Information
ProviderLanguage
Oxymetazoline English
Oxymetazoline Usage And Synthesis
OriginatorNasivin,Merck,W. Germany ,1961
UsesVasoconstrictor, used as a nasal decongestant.
UsesOxymetazoline is used for the same indications as naphazoline, primarily for rhinitis.
Manufacturing Process10 grams 2,6-dimethyl-3-hydroxy-4-tertiary butylbenzylcyanide (produced by chloromethylation of 2,4-dimethyl-6-tertiary butyl-phenol with formaldehyde and HCl and conversion of the substituted benzyl chloride with NaCN; crystals, from alcohol, melting at 135° to 137°C) and 10.7 grams ethylenediaminemono-p-toluenesulfonate are heated in an oil bath to approximately 235°C for 1? hours, whereby ammonia is evolved. The free base is obtained from the p-toluene-sulfonic acid imidazoline salt which is difficultly soluble in water, by conversion with 50 cc of a 10% NaOH solution. Said base is recrystallized from benzene, and 7.5 grams (62% of the theoretical yield) 2-(2',6'-dimethyl3'-hydroxy-4'-tertiary butylbenzyl)-2-imidazoline, MP 180° to 182°C, are obtained. By dissolving the free base in an ethyl alcohol solution of hydrochloric acid and adding ether, the hydrochloride can be produced in the usual manner. Said hydrochloride melts, when recrystallized from alcoholic ether, at 300° to 303°C and is decomposed
Brand nameOcuclear (Schering-Plough); Visine (Pfizer).
Therapeutic FunctionNasal decongestant
Safety ProfilePoison by ingestion and subcutaneous routes. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx.
SynthesisOxymetazoline, 6-tert-butyl-3(2-imidazolin-2-ilmethyl)-2,4-dimethylphenol (11.1.39), is synthesized by chloromethylation of 6-tert-butyl-2,4-dimethylphenol and the further transformation of the resulting chloromethyl derivative (11.1.37) into a nitrile (11.1.38). The reaction of this with ethylendiamine gives oxymetazoline (11.1.39) [41,42].
Enzyme inhibitorThis vasoconstrictor and nasal decongestant (FW = 260.38 g/mol; CAS 1491-59-4), systematically named as 6-t-butyl-3-(4,5-dihydro-1H-imidazol- 2-ylmethyl)-2,4-dimethylphenol, is a partial a2A-adrenergic agonist as well as a 5-HT1A, 5-HT1B, and 5-HT1D serotonin receptor agonist. It is an overthe-counter drug that is most often used topically to treat rhinitis and sinusitis. Oxymetazoline exerts a dose-dependent inhibitory effect on total iNOS activity, as indicated by nitrite/nitrate formation, and this effect is attributable to inhibition of enzyme induction rather than direct inhibition of the enzyme itself.
Oxymetazoline Preparation Products And Raw materials
Raw materialsSodium cyanide-->Hydrochloric acid-->Ethylenediamine-->Sodium hydroxide-->Formaldehyde-->p-Toluenesulfonic acid-->Oxymetazoline hydrochloride

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