Tolazoline

Tolazoline Basic information
Product Name:Tolazoline
Synonyms:TIMTEC-BB SBB003964;TOLAZOLINE;Tolazolin;Vasimid;Vasodil;Vasodilatan;1H-Imidazole, 4,5-dihydro-2-(phenylmethyl)-;2-Benzyl-2-imidazoline, 2-Benzyl-4,5-dihydro-1H-imidazole, Tolazoline
CAS:59-98-3
MF:C10H12N2
MW:160.22
EINECS:200-448-9
Product Categories:
Mol File:59-98-3.mol
Tolazoline Structure
Tolazoline Chemical Properties
Melting point 66-69 °C(lit.)
Boiling point 188°C/20mmHg(lit.)
density 1.0849 (rough estimate)
refractive index 1.6392 (estimate)
storage temp. 2-8°C
solubility alcohol: freely soluble
pkapKa 10.3(H2O t undefined I = 0.1) (Uncertain)
form Solid
color Crystals from pet ether
Merck 14,9506
CAS DataBase Reference59-98-3(CAS DataBase Reference)
NIST Chemistry Reference1H-Imidazole, 4,5-dihydro-2-(phenylmethyl)-(59-98-3)
EPA Substance Registry System1H-Imidazole, 4,5-dihydro-2-(phenylmethyl)- (59-98-3)
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 26-28-36/37/39-45
WGK Germany 3
RTECS NJ1925000
HS Code 2933299090
Toxicitycyt-ham:lng 62,500 mg/L GMCRDC 27,95,81
MSDS Information
ProviderLanguage
SigmaAldrich English
Tolazoline Usage And Synthesis
OriginatorPriscoline,Ciba,US,1948
UsesTolazoline is used for treating stable forms of pulmonary hypertension in newborns, and in cases where systemic arterial oxygenation cannot be achieved in the usual manner under careful observation of professionals.
UsesReactant for synthesis of imidazoline-containing drug
DefinitionChEBI: A member of the class of imidazoles that is 4,5-dihydro-1H-imidazole substituted by a benzyl group.
Manufacturing ProcessThe phenyl-acetiminoether hydrochloride of the formula from 12 parts of benzylcyanide and ethanol and HCl is mixed with 8 parts of ethylenediamine hydrate which has been diluted with little alcohol, whereby the crystals go into solution. The whole is then heated on the water-bath until the ammonia odor has disappeared, cooled, concentrated caustic potash solution added, and the separated oil extracted with ether. The solution is dried with potassium carbonate and potassium hydroxide. After evaporation a pale oil is left which distills at 147°C under a pressure of 9 mm and which solidifies in the condenser to a white crystalline mass. The yield amounts to 90% of the theory. The hydrochloride melts at 168° to 170°C.
Therapeutic FunctionVasodilator
General Description2-Benzylimidazoline is an active vasodilator.
PharmacologyTolazoline is a weak, reversible α-adrenoblocker that lowers resistance of peripheral blood vessels and elevates venous capacity. However, it also exhibits β-adrenomimetic activity, which consists of the stimulation of cardiac work and is manifest as tachycardia, cholinergic activity, which consists of stimulation of the gastrointestinal tract, and histamine-like activity, which consists of stimulation of gastric secretion.
Safety ProfilePoison by ingestion,intraperitoneal, and intravenous routes. Mutation data reported. When heated to decomposition it emits toxicfumes of NOx.
SynthesisTolazoline, 2-benzyl-2-imidazoline (12.2.7), is synthesized by the heterocyclation of the ethyl ester of iminophenzylacetic acid with ethylendiamine (12.2.6), which forms the desired product (12.2.7) [32¨C35]. The structure of tolazoline is strikingly similar to |á-adrenergic agonists, which are antiedema sympathomimetics.

Synthesis_59-98-3

Tolazoline Preparation Products And Raw materials
Raw materialsBenzeneacetonitrile-->Ethanol-->Ethylenediamine
1,1'-Carbonyldiimidazole Tolazoline 2-METHYL-2-IMIDAZOLINE Imidocarb dipropionate 1-Methylimidazole Benzyl chloride Benzyltriethylammonium chloride Imidazoline inhibitor 1,3-Dimethyl-2-imidazolidinone Dibenzylideneacetone Benzyl alcohol Benzyltrimethylammonium chloride Tetryzoline Imidazole Imidazolidine Benzyl Dihydromyrcenol 2-Phenyl-2-imidazoline

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