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(±)-Isoproterenol Sulfate, also known as isoprenaline, is a synthetic catecholamine and non-selective beta-adrenergic agonist. It possesses the ability to stimulate the beta-adrenergic receptors in the heart and lungs, leading to an increase in heart rate and bronchodilation.
Used in Pharmaceutical Industry:
(±)-Isoproterenol Sulfate is used as a potent bronchodilator and cardiotonic agent for the treatment of various cardiovascular and respiratory conditions, such as bradycardia, heart block, and bronchospasm.
Used in Cardiovascular Treatment:
(±)-Isoproterenol Sulfate is used as a medication to increase heart rate and improve cardiac function in patients with bradycardia and heart block.
Used in Respiratory Treatment:
(±)-Isoproterenol Sulfate is used as a bronchodilator to alleviate bronchospasm and improve lung function in patients with respiratory conditions.
Used in Emergency Medicine:
(±)-Isoproterenol Sulfate is used as an emergency medication to manage severe bradycardia and heart block situations, where an immediate increase in heart rate is required.

114-45-4

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114-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114-45-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114-45:
(5*1)+(4*1)+(3*4)+(2*4)+(1*5)=34
34 % 10 = 4
So 114-45-4 is a valid CAS Registry Number.

114-45-4Relevant academic research and scientific papers

Method for preparing isoproterenol sulfate dihydrate

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Paragraph 0021, (2017/09/01)

The invention relates to a method for preparing isoproterenol sulfate dihydrate. The method comprises the following steps: (1) preparation of 2-bromo-1-(3, 4-dihydroxy phenyl)-ethanone; (2) preparation of isoproterenol ketone hydrochloride; and (3) preparation of isoproterenol sulfate dihydrate. The method disclosed by the invention adopts a reaction system of bromoacetyl bromide and aluminium chloride instead of a reaction system of monochloro acetic acid and phosphorus oxychloride, so that the method has the advantages that the environmental protection cost is reduced; the reaction yield is increased; the industrial production is benefited; the reaction condition is mild; the catalyst quantity is little; and the process is simple. Compared with conventional synthetic processes, the method disclosed by the invention has obvious economic benefit and environmental benefit.

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