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Isoproterenol sulfate

Isoproterenol sulfate structure

Isoproterenol sulfate 

structure
  • CAS No:

    299-95-6

  • Formula:

    C11H17NO3.1/2H2O4S

  • Chemical Name:

    Isoproterenol sulfate

  • Synonyms:

    1,2-Benzenediol,4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]-,sulfate (2:1);Benzyl alcohol,3,4-dihydroxy-α-[(isopropylamino)methyl]-,sulfate (2:1) (salt);1,2-Benzenediol,4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]-,sulfate (2:1) (salt);1-(3,4-Dihydroxyphenyl)-2-isopropylaminoethanol sulfate (2:1);Isoprenaline sulfate (2:1);Isoproterenol sulfate (2:1);Isopropylnoradrenaline sulfate;Isoproterenol sulfate;Isoprenaline sulfate;N-Isopropylnorepinephrine sulfate;Aleudrin;Novodrin;Medihaler-ISO;Novodrine;dl-α-3,4-Dihydroxyphenyl-β-iso-propylaminoethanol sulfate;dl-Isoprenaline sulfate;(±)-Isoprenaline sulfate;dl-Isoproterenol sulfate;(±)-Isoproterenol sulfate;114-45-4;750-95-8

  • Categories:

    Active Pharmaceutical Ingredients  >  Respiratory Drugs

Description

Isopropyl analog of EPINEPHRINE; beta-sympathomimetic that acts on the heart, bronchi, skeletal muscle, alimentary tract, etc. It is used mainly as bronchodilator and heart stimulant.

Isoproterenol sulfate Basic Attributes

520.6

520.209045

206-085-2

2922509090

Characteristics

228

3.46820

180 °C

417.5ºC at 760 mmHg

179.7ºC

almost transparency

Safety Information

22

44

DO2273000

Drug Information

Agents that cause an increase in the expansion of a bronchus or bronchial tubes. (See all compounds classified as Bronchodilator Agents.)|Drugs that selectively bind to and activate beta-adrenergic receptors. (See all compounds classified as Adrenergic beta-Agonists.)|Agents that have a strengthening effect on the heart or that can increase cardiac output. They may be CARDIAC GLYCOSIDES; SYMPATHOMIMETICS; or other drugs. They are used after MYOCARDIAL INFARCT; CARDIAC SURGICAL PROCEDURES; in SHOCK; or in congestive heart failure (HEART FAILURE). (See all compounds classified as Cardiotonic Agents.)|Drugs that mimic the effects of stimulating postganglionic adrenergic sympathetic nerves. Included here are drugs that directly stimulate adrenergic receptors and drugs that act indirectly by provoking the release of adrenergic transmitters. (See all compounds classified as Sympathomimetics.)

4-(1-Hydroxy-2-((1-methylethyl)amino)ethyl)-1,2-benzenediol

Isoproterenol sulfate Use and Manufacturing

Uses

Bronchodilator.

Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients

Computed Properties

Molecular Weight:520.6
Hydrogen Bond Donor Count:10
Hydrogen Bond Acceptor Count:12
Rotatable Bond Count:8
Exact Mass:520.20906652
Monoisotopic Mass:520.20906652
Topological Polar Surface Area:228
Heavy Atom Count:35
Complexity:268
Undefined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes

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