Salbutamol | |
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Salts [] | |
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Salbutamol sulfate | |
Salbutamol hydrochloride | |
Salbutamol tartrate | |
Esters [] | |
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Salbutamol acetate | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C13H21NO3[1] |
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Molecular mass | 239.31 g/mol[1] |
Appearance | White to off-white crystalline solid[1] |
Predicted LogP | 0.3[1] |
Melting point | 147-149[1] |
Solubility | Soluble in ethanol, sparingly soluble in water, and very soluble in chlorform.[1] |
Chirality | racemic[2] |
Identifiers [] | |
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IUPAC name | 4-[2-(tert-butylamino)-1-hydroxyethyl]-2-(hydroxymethyl)phenol[1] |
SMILES | CC(C)(C)NCC(C1=CC(=C(C=C1)O)CO)O[1] |
InChI | InChI=1S/C13H21NO3/c1-13(2,3)14-7-12(17)9-4-5-11(16)10(6-9)8-15/h4-6,12,14-17H,7-8H2,1-3H3[1] |
InChIKey | NDAUXUAQIAJITI-UHFFFAOYSA-N[1] |
Dosing |
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Salbutamol
Salbutamol (also known as albuterol, Ventoline, Broncovaleas, dl-Albuterol, dl-Salbutamol, Salbutamolum, Asthalin, Cobutolin, Salbulin or Salbuvent) is a sympathomimetic substance of the phenylethanolamine class.
Chemistry
Salbutamol is typically found in the form of its sulfate, hydrochloride and tartrate salts or its acetate ester.
Stereochemistry
(RS)-Salbutamol is a racemic mixture of the optical stereoisomers:
Stereoisomers [] |
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Subjective effects
See also
External links
- Salbutamol / (-)-Salbutamol (Wikipedia)
- Salbutamol / (+)-Salbutamol / (-)-Salbutamol (Wikidata)
- Salbutamol / (-)-Salbutamol (DrugBank)
- Salbutamol / (+)-Salbutamol / (-)-Salbutamol (PubChem)
- Salbutamol / (+)-Salbutamol / (-)-Salbutamol (ChEMBL)
- Salbutamol / (-)-Salbutamol (ChEBI)
- Salbutamol / (+)-Salbutamol / (-)-Salbutamol (Common Chemistry)
- Salbutamol (HMDB)
- Salbutamol / (-)-Salbutamol (KEGG)
- Salbutamol / (+)-Salbutamol / (-)-Salbutamol (UNII)
- Salbutamol / (+)-Salbutamol / (-)-Salbutamol (EPA DSSTox)