Salbutamol
Compound with spectra: 2 NMR, 1 FTIR, 1 Raman, and 5 MS (GC)
| SpectraBase Compound ID | DrNDZVtibgH |
|---|---|
| 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 |
| InChIKey | NDAUXUAQIAJITI-UHFFFAOYSA-N |
| Mol Weight | 239.31 g/mol |
| Molecular Formula | C13H21NO3 |
| Exact Mass | 239.152144 g/mol |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. Portions provided by AAFS, Toxicology Section. All Rights Reserved. |
|---|---|
| Source of Spectrum | Mass Spectrometry Committee of the Toxicology Section of the American Academy of Forensic Sciences |
| Copyright | Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved. |
|---|---|
| Source of Spectrum | Chemical Concepts, A Wiley Division, Weinheim, Germany |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | NP-6-4472-0 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | JZ-1992-618-0 |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Spectrum Chemical Manufacturing Corp. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | AL155 |
| Copyright | Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved. |
|---|---|
| Solvent | D2O |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Spectrum Chemical Manufacturing Corp. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | AL155 |
- Albuterol
- 1-(3'-HYDROXYMETHYL,4'-HYDROXY-PHENYL)-2-TERT.-BUTYLAMINOETHAN-1-OL
- 4-[2-(tert-Butylamino)-1-hydroxyethyl]-2-(hydroxymethyl)phenol
- 1-(3-Hydroxymethyl-4-hydroxyphenyl)-2-tert-butylamino-ethanol
2-Amino-5-[1-hydroxy-2-(isopropylamino)ethyl]benzonitrile
1-(4-HYDROXY-3-METHOXYPHENYL)-BUTAN-1,4-DIOL
2-(2-Hydroxy-5-methylphenyl)-N,N-diisopropylacetamide
3-Me-4-MeO-PEA PFP
4-(2-amino-2-methylpropyl)-alpha-(dimethylamino)-o-cresol
3-allyl-4-hydroxybenzoic acid, methyl ester
4-HYDROXY-3-PRENYLBENZOIC-ACID
a-(trichloromethyl)vanillyl alcohol
4-(2-amino-1-hydroxy-butyl)benzene-1,2-diol
2,4-Dibenzylphenol
| Title | Journal or Book | Year |
|---|---|---|
| Carbon-13 N.M.R. studies of some β-adrenergic agents | Australian Journal of Chemistry | 1978 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.
KnowItAll IR, Raman, and UV-Vis Spectral Libraries
Author: Wiley
The KnowItAll IR, Raman, and UV-Vis spectral libraries offer access to the world's largest collection of IR, Raman, and UV-Vis spectra, including the renowned Sadtler spectra. The libraries include a wide range of compounds from pure organics to industrial compounds. Learn more.
KnowItAll Mass Spectral Library
Author: Wiley
The KnowItAll Mass Spectral Library offers a comprehensive collection of mass spectra, including the renowned Wiley Registry, and access to a wide range of compounds including pure organics, drugs, steroids, additives, geochemicals, petrochemicals, biomarkers, and more. Learn more.
Maurer, Meyer, Helfer, Weber: LC-HR-MS & MS Library of Drugs, Poisons, and Their Metabolites
Author: Hans H. Maurer, Markus Meyer, Andreas G. Helfer, Armin A. Weber
Developed by toxicologist Hans H. Maurer and his team, the Maurer/Meyer/Helfer/Weber LC-HR-MS/MS Library of Drugs, Poisons, and Their Metabolites consists of spectra for parent drugs or poisons, and their metabolites or artifacts, in various compound classification groups. This metabolite-based library helps minimize the risk of false negative LC-MS results. Learn more.