(±)-Isoproterenol hydrochloride
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(±)-Isoproterenol hydrochloride
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CAS No:
51-30-9
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Formula:
C11H17NO3.ClH
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Chemical Name:
(±)-Isoproterenol hydrochloride
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Synonyms:
1,2-Benzenediol,4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]-,hydrochloride (1:1);Benzyl alcohol,3,4-dihydroxy-α-[(isopropylamino)methyl]-,hydrochloride;1,2-Benzenediol,4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]-,hydrochloride;Protocatechuyl alcohol,α-(isopropylaminomethyl)-,hydrochloride;α-(Isopropylaminomethyl)-3,4-dihydroxybenzyl alcohol hydrochloride;3,4-Dihydroxy-α-(isopropylaminomethyl)benzyl alcohol hydrochloride;Isoprenaline hydrochloride;Isoproterenol hydrochloride;Isuprel;Isopropylarterenol hydrochloride;Euspiran;Isadrine;Isoprenaline chloride;Saventrine;Proternol;1-(3,4-Dihydroxyphenyl)-2-(isopropylamino)ethanol hydrochloride;(±)-Isoprenaline hydrochloride;dl-Isopropylnoradrenaline hydrochloride;(±)-Isopropylnoradrenaline hydrochloride;dl-Isopropylnorepinephrine hydrochloride;dl-Isoproterenol hydrochloride;(±)-Isoproterenol hydrochloride;dl-Isoprenaline hydrochloride;dl-Isadrine hydrochloride;DL-Isoproterenol hydrochloride;DL-Isoprenaline hydrochloride;Asthpul;Vapo-Iso;Suscardia;Mistarel;Isomenyl;Aerolone;Aerotrol;Isovon;NSC 37745;NSC 89747;Isoprel;949-36-0;1336-89-6;71249-42-8
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CAS No:
Description
Isoprenaline hydrochloride is a non-selective beta-adrenergic receptor agonist with potent peripheral vasodilator, bronchodilator, and cardiac stimulating activities.
Isoproterenol hydrochloride is an odorless white crystalline powder. Slightly bitter taste. Aqueous solutions turn brownish-pink upon prolonged exposure to air. (NTP, 1992)
Isoproterenol hydrochloride is an odorless white crystalline powder. Slightly bitter taste. Aqueous solutions turn brownish-pink upon prolonged exposure to air. (NTP, 1992)|DL-Isoprenaline hydrochloride is a member of catechols.|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 hydrochloride Basic Attributes
247.72
247.097519
200-089-8
757079|89747|37745
DTXSID6025486
29225090
Characteristics
72.7
2.32210
Isoproterenol hydrochloride is an odorless white crystalline powder. Slightly bitter taste. Aqueous solutions turn brownish-pink upon prolonged exposure to air. (NTP, 1992)
1.324 g/cm3
170-172 °C (decomp)
417.5ºC at 760 mmHg
179.7ºC
H2O: soluble
Store at RT
LD50 oral in rabbit: 3070mg/kg
May be sensitive to exposure to air and light. (NTP, 1992). Water soluble.
Alcohols and Polyols
An acid organic salt. Materials in this group are generally soluble in water. The resulting solutions contain moderate concentrations of hydrogen ions and have pH's of less than 7.0. They react as acids to neutralize bases. These neutralizations generate heat, but less or far less than is generated by neutralization of inorganic acids, inorganic oxoacids, and carboxylic acid. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible.
Safety Information
NONH for all modes of transport
2
36/37/38
26-36
DO1925000
Xi
Stable, but may be air and light sensitive. Incompatible with strong oxidizing agents.
P261-P305 + P351 + P338
H315-H319-H335
Flash point data for this chemical are not available. It is probably combustible. (NTP, 1992)
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 40 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Fires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)
SMALL SPILLS AND LEAKAGE: If you spill this chemical, you should dampen the solid spill material with water, then transfer the dampened material to a suitable container. Use absorbent paper dampened with water to pick up any remaining material. Seal your contaminated clothing and the absorbent paper in a vapor-tight plastic bag for eventual disposal. Wash all contaminated surfaces with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned. STORAGE PRECAUTIONS: You should protect this chemical from exposure to light. Keep the container tightly closed under an inert atmosphere, and store under refrigerated temperatures. (NTP, 1992)
RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)
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 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.)|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.)
SYMPTOMS: Symptoms of exposure to this compound may include tremors, nervous apprehension, palpitations of the heart, epigastric distress, cardiac arrhythmias, myocardial necrosis, cardiac arrest, tachycardia, headache, flushing of the skin, anginal pain, nausea, dizziness, weakness, and sweating. (NTP, 1992)
EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment. INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing. INGESTION: DO NOT INDUCE VOMITING. If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center. Be prepared to transport the victim to a hospital if advised by a physician. If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body. DO NOT INDUCE VOMITING. IMMEDIATELY transport the victim to a hospital. (NTP, 1992)
4-(1-Hydroxy-2-((1-methylethyl)amino)ethyl)-1,2-benzenediol
(±)-Isoproterenol hydrochloride Use and Manufacturing
Isoproterenol is a non-selective beta-adrenergic agonist. Isoproterenol is used in the treatment of bradycardia; bronchodilator.
Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients
Computed Properties
Molecular Weight:247.72
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:247.0975211
Monoisotopic Mass:247.0975211
Topological Polar Surface Area:72.7
Heavy Atom Count:16
Complexity:187
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
This product is a β-receptor agonist, which has a strong stimulatory effect on both β1 and β2 receptors, and has almost no effect on α receptors. Main effects: It acts on the heart β1 receptors to enhance cardiac contractility, increase heart rate, accelerate conduction, increase cardiac output and myocardial oxygen consumption. It acts on the vascular smooth muscle β2 receptors to significantly dilate skeletal muscle blood vessels, and the kidneys, mesenteric blood vessels and coronary arteries also dilate to varying degrees, and the total vascular resistance is reduced. Its cardiovascular effects lead to increased systolic blood pressure, decreased diastolic blood pressure, and increased pulse pressure difference. It acts on the bronchial smooth muscle β2 receptors to relax bronchial smooth muscle. It promotes the decomposition of glycogen and fat and increases tissue oxygen consumption.
Registered Holders
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MICRO LABS LTD
Active
United States
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EMCURE PHARMACEUTICALS LTD
Active
United States
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Sterling Wisconsin LLC
Active
United States
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