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23031-32-5

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23031-32-5 Usage

Description

Terbutaline Sulfate is a β2-adrenergic receptor agonist, derived from Terbutaline Hemisulfate Salt, which is a more potent and selective β2-selective analogue of metaproterenol. It is a white or almost white, crystalline powder with good oral bioavailability and is resistant to COMT and slowly metabolized by MAO. Terbutaline Sulfate is available in various forms such as tablets, solutions for injection, and inhalation.

Uses

Used in Pharmaceutical Industry:
Terbutaline Sulfate is used as a bronchodilator for the treatment of asthma and other respiratory conditions. It works by relaxing the muscles in the airways and increasing airflow to the lungs, providing relief from asthma symptoms.
Used in Sports Performance Enhancement:
Terbutaline Sulfate is used as a β2-adrenergic agonist to enhance physical performance in athletes. It is known to increase the heart rate, blood pressure, and blood flow, which can improve athletic performance.
Used in Analytical and Forensic Applications:
Terbutaline (hemisulfate) is used as an analytical reference standard in forensic applications and as a general research tool for studying the effects of β2-adrenergic receptor agonists.
Used in Anti-Asthma Treatment:
Terbutaline Sulfate is used as an anti-asthmatic agent for the management of asthma symptoms. It helps in reducing inflammation and constriction of the airways, providing relief to patients suffering from asthma.

Therapeutic Function

Bronchodilator

Clinical Use

Beta2 -adrenoceptor agonist: Reversible airways obstruction

Veterinary Drugs and Treatments

Terbutaline is used as a bronchodilating agent in the adjunctive treatment of cardiopulmonary diseases (including tracheobronchitis, collapsing trachea, pulmonary edema, and allergic bronchitis) in small animals. It may be of some benefit in treating bradyarrhythmias in dogs and cats. Terbutaline has been used occasionally in horses for its bronchodilating effects, but adverse effects, short duration of activity after IV administration and poor oral absorption have limited its use. It has been shown to be useful as a diagnostic agent to diagnose anhidrosis in horses after intradermal injection. Oral and intravenous terbutaline has been used successfully in humans for the inhibition of premature labor clinical signs.

Drug interactions

Potentially hazardous interactions with other drugs Effect may be diminished by beta-blockers. Theophylline: increased risk of hypokalaemia.

Metabolism

Terbutaline undergoes extensive first-pass metabolism by sulphate (and some glucuronide) conjugation in the liver and the gut wall. It is excreted in the urine and faeces partly as the inactive sulphate conjugate and partly as unchanged terbutaline, the ratio depending upon the route by which it is given.

Check Digit Verification of cas no

The CAS Registry Mumber 23031-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,3 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23031-32:
(7*2)+(6*3)+(5*0)+(4*3)+(3*1)+(2*3)+(1*2)=55
55 % 10 = 5
So 23031-32-5 is a valid CAS Registry Number.
InChI:InChI=1/2C12H19NO3.H2O4S/c2*1-12(2,3)13-7-11(16)8-4-9(14)6-10(15)5-8;1-5(2,3)4/h2*4-6,11,13-16H,7H2,1-3H3;(H2,1,2,3,4)

23031-32-5 Well-known Company Product Price

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  • Sigma-Aldrich

  • (T0050000)  Terbutaline sulfate  European Pharmacopoeia (EP) Reference Standard

  • 23031-32-5

  • T0050000

  • 1,880.19CNY

  • Detail

23031-32-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[2-(tert-butylamino)-1-hydroxyethyl]benzene-1,3-diol,sulfuric acid

1.2 Other means of identification

Product number -
Other names Terbutaline sulfate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:23031-32-5 SDS

23031-32-5Relevant articles and documents

Preparation method of terbutaline sulfate and B crystal form thereof

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Paragraph 0020; 0039; 0048-0053; 0054; 0060-0063, (2021/01/29)

The invention relates to a preparation method of terbutaline sulfate and a B crystal form thereof, which comprises the following steps: sequentially carrying out bromination, reduction reaction and substitution reaction to obtain 1-[3, 5-bis (benzyloxy) phenyl]-2-(tert-butylamino) ethanol; reacting 1-[3, 5-di (benzyloxy) phenyl]-2-(tert-butylamino) ethanol with a reducing agent and a catalyst, performing salifying with sulfuric acid to obtain a terbutaline sulfate crude product, and crystallizing the terbutaline sulfate crude product under a heating reflux condition to obtain the terbutaline sulfate medicinal B crystal form. Raw materials and auxiliary materials used in the method are cheap and easy to obtain, highly toxic and explosive reagents are avoided in the reaction process, the whole reaction route is short, operation is easy and convenient, reaction conditions are mild and safe, the yield of the obtained finished product terbutaline sulfate and the medicinal B crystal form thereof is high, the yield of terbutaline sulfate is 83% or above, and the yield of the medicinal B crystal form is 70% or above, and industrialized production can be achieved easily.

Preparation method of terbutaline sulfate

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Paragraph 0017; 0029; 0033-0034; 0038-0039; 0043-0044; 0048, (2020/04/29)

The invention discloses a preparation method of terbutaline sulfate, wherein the method comprises the following steps: carrying out a bromination reaction on 3,5-dihydroxyacetophenone as a raw material by using a bromination reagent without hydroxyl protection, carrying out reduction and ring closing, carrying out a ring-opening reaction with tert-butylamine, and finally forming a salt with sulfuric acid to obtain terbutaline sulfate. According to the method, the defects of requirement of deprotection after hydroxyl protection, use of various high-risk highly toxic reagents, long reaction stepand low yield in the prior art are overcome.

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