| Weight | 239.315 g/mol |
|---|---|
| Formula | C13H21NO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
Salbutamol (18559-94-9)
Albuterol · Ventolin · Proventil
Score:
#929 in Biology
,
#1026 in Chemistry
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- Association between genetic polymorphisms of the beta2-adrenoceptor and response to albuterol in children with and without a history of wheezing. (Journal of Clinical Investigation, 1997)
- Use of regularly scheduled albuterol treatment in asthma: genotype-stratified, randomised, placebo-controlled cross-over trial. (The Lancet, 2004)
- The effect of polymorphisms of the 2-adrenergic receptor on the response to regular use of albuterol in asthma (American Journal of Respiratory and Critical Care Medicine, 2000)
- Comparative effects of inhaled salbutamol, sodium cromoglycate, and beclomethasone dipropionate on allergen-induced early asthmatic responses, late asthmatic responses, and increased bronchial responsiveness to histamine (The Journal of Allergy and Clinical Immunology, 1987)
- Serevent nationwide surveillance study: comparison of salmeterol with salbutamol in asthmatic patients who require regular bronchodilator treatment. (BMJ, 1993)
- Comparison of Regularly Scheduled with As-Needed Use of Albuterol in Mild Asthma (The New England Journal of Medicine, 1996)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Albuterol
- Ventolin
- Proventil
- Albuterol Sulfate
- Sultanol
- 2-t-Butylamino-1-(4-hydroxy-3-hydroxy-3-hydroxymethyl)phenylethanol
-
SMILESCC(C)(C)NCC(C1=CC(=C(C=C1)O)CO)O
-
InChIKeyNDAUXUAQIAJITI-UHFFFAOYSA-N
- Pubchem - Salbutamol
- Wikipedia - salbutamol
Salbutamol, also known as albuterol and marketed as Ventolin among other names, is a medication that opens up the medium and large airways in the lungs. It is used to treat asthma including asthma attacks, exercise-induced bronchoconstriction, and chronic obstructive pulmonary disease (COPD). It may also be used to treat high blood potassium levels.
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Most-cited Publications
Areas of Application
Safety
Trends
Alternate Names
External Links
Synthesis
Reactant
+
5330-38-1
(Grignard alcohol)
Reactant
+
tert-Butylamine
(Reductive amination)
Reactant
+
2-Chloro-2-methylpropane
(Alkylation of primary amines)
salicyl alcohol
+
Reactant
(Friedel-Crafts alkylation)
Tert-butylboronic Acid
+
Reactant
(Chan-Lam coupling reaction)
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(2493-84-7)
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(140-66-9)
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1'-HYDROXYSAFROLE
(5208-87-7)
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(55-31-2)
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(326-61-4)
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(1034-01-1)
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trans-4-tert-Butylcyclohexanecarboxylic acid
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(103-05-9)
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3',4'-Dihydroxyacetophenone
(1197-09-7)
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3 suppliers
propanil
(709-98-8)
7 alternate names
3 safety hazards
3 suppliers
diuron
(330-54-1)
7 alternate names
5 safety hazards
3 suppliers
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(93-72-1)
7 alternate names
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3 suppliers
chlorpropham
(101-21-3)
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2 safety hazards
3 suppliers
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(61-76-7)
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(1197-21-3)
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(5932-68-3, 97-54-1)
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4 safety hazards
3 suppliers
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(80-15-9)
7 alternate names
9 safety hazards
3 suppliers
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(5471-51-2)
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MONOLINURON
(1746-81-2)
7 alternate names
3 safety hazards
3 suppliers
2,6-DI-TERT-BUTYLPHENOL
(128-39-2)
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(151-06-4)
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5 safety hazards
3 suppliers
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(51022-70-9)
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(4938-72-1)
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(104-40-5, 68081-86-7, 25154-52-3)
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3 suppliers
274671-61-3
(274671-61-3)
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3 suppliers
4-OCTYLPHENOL
(71902-25-5, 1806-26-4)
7 alternate names
2 safety hazards
3 suppliers
Compound 5353
(2282-34-0)
7 alternate names
3 suppliers
LINAMARIN
(554-35-8)
7 alternate names
3 suppliers
101-96-2
(101-96-2)
7 alternate names
3 suppliers
Salbutamol
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