22254-24-6 Usage
Description
Ipratropium bromide, also known as Atrovent, is a quaternary ammonium derivative of atropine. It is a nonselective muscarinic acetylcholine receptor antagonist and a bronchodilator. Ipratropium bromide is freely soluble in water and ethanol but insoluble in chloroform and ether. The salt is stable in neutral and acidic solutions but rapidly hydrolyzed in alkaline solutions. It is a white powder and is used as an anticholinergic drug to block muscarinic cholinergic receptors in the smooth muscles of the bronchi in the lungs, providing relief in chronic obstructive pulmonary disease and acute asthma.
Uses
Used in Pharmaceutical Industry:
Ipratropium bromide is used as a bronchodilator for treating and preventing minor and moderate bronchial asthma, especially asthma accompanied by cardiovascular system diseases. It exhibits broncholytic action by reducing cholinergic influence on bronchial musculature (m-cholinoblocking action), relieving bronchial spasms.
Used in Respiratory Treatment:
Ipratropium bromide is used as an anticholinergic drug for providing relief in chronic obstructive pulmonary disease and acute asthma by blocking muscarinic cholinergic receptors in the smooth muscles of the bronchi in the lungs, which opens the bronchi and improves respiratory function.
Pharmacology and toxicology
Ipratropium bromide is also known as isoprenaline, isopropyl atropine, isopropyl scopolamine, isopropyl atropine, ipratropium bromide, isopropyl atropine, isopropyl atropine bromide, ipratropium bromide, bromo ipratropium bromide. It is a white crystalline powder with bitter taste and melting point of 232℃-233℃. It is soluble in water, slightly soluble in ethanol and insoluble in other organic solvents. Chemical name is Brominated alpha (methylol) - phenylacetic acid -8- methyl -8- isopropyl- azacyclo [3, 2, 1]-3- octyl. It is an anticholinergic drug and can relax the bronchial smooth muscle.It has an antiasthmatic effect on chronic obstructive pulmonary disease.The effect is obvious, fast and enduring. Isopatropium also has the effect of controlling the secretion of the mucous glands and improving the ciliated movement, thereby reducing the obstruction of sputum to improve ventilation. At the same time, the decrease of sputum also relieves bronchospasm caused by bronchial irritation.It is used for the prevention and treatment of bronchial asthma and asthma type chronic bronchitis. Especially it is applicable to patients with a beta agonist that produces muscle tremor, tachycardia and can not tolerate such kind of drugs. The combination of this product and beta agonist can enhance the efficacy of each other.For example, it can be combined with fenoterol into aerosol (BERODU - AL) for treating asthma, chronic bronchitis and emphysema.Compared with beta adrenergic receptor stimulants (such as isopropylepinephrine), this product has less side effects on the cardiovascular system.
Compared with the beta 2- receptor stimulant (such as broncovaleas ), this product has a strong regulating effect on the amount of phlegm.
Indication
For the prevention and treatment of bronchial asthma and asthma type chronic bronchitis. Especially it is applicable to the patients with a beta agonist that produces muscle tremor, tachycardia and can not tolerate such drugs. The combination of this product and beta agonist can enhance the efficacy of each other. For example, it can be combined with fenoterol into aerosol (BERODU - AL) for treating asthma, chronic bronchitis and emphysema.
Precaution
Prohibition It is prohibited for people who are allergic to soy lecithin or related foods such as soya and peanuts and those who are allergic to atropine or its derivatives or other ingredients of this product. It is also prohibited for the patients with hypertrophic obstructive cardiomyopathy, fast arrhythmia and pyloric obstruction.
Cautious use It should be used in caution for patients with a tendency to narrow angle glaucoma, a benign prostatic hyperplasia, or a bladder neck obstruction.
The use of beta adrenergic stimulants or xanthine agents can enhance the bronchiectasis of the drug.
The most common non respiratory adverse reactions are headache, nausea, dry mouth, dysphonia, vertigo, anxiety, tachycardia, skeletal muscle fine tremor and palpitation.
If the atomized ipratropium bromide is used alone or in combination with adrenaline beta 2- receptor agonist, when the atomizer enters the eye, it may have ocular complications, such as large pupil, increased intraocular pressure, angle closure glaucoma, and eye pain.
Drug overdose
Cholinesterase inhibitor can be used in the treatment of severe anticholinergic drug poisoning.
Adverse reaction
The adverse reaction of ipratropium bromide is similar to atropine, which can cause palpitation, headache, dizziness, nervousness, nausea and vomiting, alimentary tract pain, tremor, blurred vision, dry mouth and cough, dysuria, respiratory symptoms aggravating and rash.
Originator
Atrovent,Boehringer Ingelheim,W. Germany,1975
Manufacturing Process
21 1.5 g (0.667 mol) of N-isopropyl-noratropine were dissolved at 60°C in
2.11 liters of absolute toluene in a 3-liter glass pressure tube. While the
solution was still warm, 95 g (1 mol) of ice-cold methylbromide were added,
and the pressure tube was sealed immediately thereafter. The reaction
mixture was kept at 60°C for four days. After one hour of standing, the
formation of crystals began. At the end of four days the crystals were
separated by vacuum filtration at 60°C, washed with 600 cc of toluene at
60°C, and dried in vacuo in a drying cabinet at 100°C. Raw yield: 263.7 g
(95.8% of theory). MP: 224°C to 225°C (decomp.). The raw product was
refluxed with 2.5 liters of chloroform for 30 minutes, vacuum filtered whilehot, washed with 200 cc of chloroform, and dried in a vacuum drying cabinet
at 100°C. Yield: 249 g (90.6% of theory). MP: 226°C to 228°C (decomp.).
The purified product was recrystallized from 1.2 liters of n-propanol, washed
with 200cc of n-propanol and dried in a vacuum drying cabinet at 100°C.
Yield: 237 g (86.15% of theory). MP: 230°C to 232°C (decomp.). By
evaporation of the mother liquor to 100 cc another 6.0 g of the pure product,
MP 230°C to 231.5°C (decomp.), were obtained.
Therapeutic Function
Bronchodilator
Biological Activity
Muscarinic antagonist, bronchodilator. N-Isopropyl salt of atropine.
Clinical Use
Ipratropium bromide is used in inhalation therapy toproduce dilation of bronchial smooth muscle for acute asthmaticattacks. The drug produces bronchodilation by competitiveinhibition of cholinergic receptors bound to smooth muscle of the bronchioles. Ipratropium may also act on thesurface of mast cells to inhibit ACh-enhanced release ofchemical mediators. The drug has a slow onset of action,within 5 to 15 minutes after being administered by inhalation,and should not be used alone for acute asthmatic attacks.The peak therapeutic effect from one dose is observedbetween 1 and 2 hours. The effects of the drug last for about6 hours. It has a half-life of 3.5 hours.
Clinical Use
Ipratropium bromide (Atrovent) is a quaternary amine
derivative that is used via inhalation in the treatment of
chronic obstructive pulmonary disease and to a lesser
extent, asthma.
Synthesis
Ipratropium bromide, 3α-hydroxy-8-isopropyl-1αH,5αH-tropanium
bromide (23.3.6), is synthesized by reacting N-isopropylnoratropine with methyl
bromide.
Veterinary Drugs and Treatments
Locally administered (inhaled) ipratropium bromide can be used
for the adjunctive treatment of bronchospastic conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 22254-24-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,5 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22254-24:
(7*2)+(6*2)+(5*2)+(4*5)+(3*4)+(2*2)+(1*4)=76
76 % 10 = 6
So 22254-24-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H30NO3.BrH/c1-14(2)21(3)16-9-10-17(21)12-18(11-16)24-20(23)19(13-22)15-7-5-4-6-8-15;/h4-8,14,16-19,22H,9-13H2,1-3H3;1H/q+1;/p-1/t16-,17?,18-,19?,21?;/m1./s1
