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Tolazoline hydrochloride

Tolazoline hydrochloride Suppliers list
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Products Intro: CAS:59-97-2
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CAS:59-97-2
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Products Intro: Product Name:Tolazoline hydrochloride
CAS:59-97-2
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Products Intro: Product Name:Tolazoline hydrochloride
CAS:59-97-2
Purity:0.98 Package:1kg,2kg,5kg,10kg,25kg

Tolazoline hydrochloride manufacturers

Tolazoline hydrochloride Basic information
Product Name:Tolazoline hydrochloride
Synonyms:2-benzyl-2-imidazolinhydrochloride;tolazolinechloride;2-benzyl-2-imidazolinmonohydrochloride;4,5-dihydro-2-(phenylmethyl)-1h-imidazolmonohydrochloride;arterodyl;benzylimidazolinehydrochloride;cloridratodi2-benzil-4,5-imidazolina;imidalinehydrochloride
CAS:59-97-2
MF:C10H13ClN2
MW:196.68
EINECS:200-447-3
Product Categories:PRISCOLINE;Intermediates & Fine Chemicals;Pharmaceuticals;Aromatics;Heterocycles
Mol File:59-97-2.mol
Tolazoline hydrochloride Structure
Tolazoline hydrochloride Chemical Properties
Melting point 172-176 °C
storage temp. Inert atmosphere,Room Temperature
solubility DMSO (Slightly, Heated), Methanol (Slightly)
form Crystalline Powder
color White to almost white
Sensitive Hygroscopic
Merck 14,9506
Stability:Hygroscopic
CAS DataBase Reference59-97-2(CAS DataBase Reference)
EPA Substance Registry SystemTolazoline hydrochloride (59-97-2)
Safety Information
Hazard Codes Xn
Risk Statements 22
Safety Statements 22
RIDADR 2811
TSCA Yes
HS Code 29332900
ToxicityLD50 orl-rat: 1200 mg/kg NIIRDN 6,511,82
MSDS Information
ProviderLanguage
ACROS English
ALFA English
Tolazoline hydrochloride Usage And Synthesis
Chemical PropertiesPale Yellow Crystalline Solid
OriginatorPriscoline,Ciba,US,1948
UsesΑn α-adrenergic antagonist. A peripheral vasodilator.
Usesa-adrenergic antagonist. A peripheral vasodilator
Usesadrenergic blocker
DefinitionChEBI: Tolazoline hydrochloride is a member of benzenes.
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.
Brand nameTolazoline is INN and BAN.
Therapeutic FunctionVasodilator
Safety ProfilePoison by ingestion, intravenous, and intraperitoneal routes. Human systemic effects by intravenous route: change in heart rate, sweating, ulceration or bleeding from duodeum, ulceration or bleeding from small intestine, unspecified vascular effects. When heated to decomposition it emits very toxic fumes of NO, and HCl.
Veterinary Drugs and Treatmentsflipping of lips); piloerection; clear lacrimal & nasal discharge; muscle fasciculations; apprehensiveness Uses/Indications Tolazoline is approved and indicated for the reversal of effects associated with xylazine in horses. It has also been used for this purpose in a variety of other species as well, but less safety and efficacy data is available.
In humans, the primary uses for tolazoline are: treatment of persistent pulmonary hypertension in newborns, adjunctive treatment and diagnosis
Tolazoline hydrochloride Preparation Products And Raw materials
Raw materialsEthylenediamine-->Benzeneacetonitrile-->Ethanol
Tag:Tolazoline hydrochloride(59-97-2) Related Product Information
ISOXAZOLIDINE HYDROCHLORIDE 2-(4-TERT-BUTYL-2,6-DIMETHYL-BENZYL)-4,5-DIHYDRO-1H-IMIDAZOLE Tungsten Clonazoline Xylometazoline hydrochloride Naphazoline hydrochloride Tolazoline hydrochloride 2-Tetralin-1-yl-4,5-dihydro-1H-imidazole hydrochloride Oxymetazoline hydrochloride Oxazoline Benzil Tolazoline Nemazoline dazadrol 2-BENZYL-2-IMIDAZOLINE HYDROCHLORIDE, (TOLAZOLINE HYDROCHLORIDE) 2-(2,3,5,6-Tetramethyl-4-nitrobenzyl)imidazoline hydrochloride 2-(4-Bromo-2,3,5,6-tetramethylbenzyl)imidazoline hydrochloride