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Merck

46725

Salbutamol

VETRANAL®, analytical standard

Synonym(s):

α-[(tert-Butylamino)methyl]-4-hydroxy-m-xylene-α,α′-diol, Albuterol

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About This Item

Empirical Formula (Hill Notation):
C13H21NO3
CAS Number:
18559-94-9
Molecular Weight:
239.31
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329757226
EC Number:
242-424-0
Beilstein/REAXYS Number:
6405698
MDL number:
MFCD00148978

Product Name

Salbutamol, VETRANAL®, analytical standard

InChI key

NDAUXUAQIAJITI-UHFFFAOYSA-N

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

SMILES string

CC(C)(C)NCC(O)c1ccc(O)c(CO)c1

grade

analytical standard

product line

VETRANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

clinical testing

format

neat

Quality Level

100

Gene Information

human ... ADRB2(154)

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Salbutamol may be used as a reference standard for the determination of salbutamol in:
  • Fish plasma by solid phase extraction (SPE) followed by analysis using liquid chromatography combined with electrospray ionization triple quadrupole mass spectrometry (ESI-LC-QqQMS).
  • Feed samples by ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) as well as supercritical fluid chromatography (SFC) with MS/MS.
  • Pig hair by HPLC in combination with ESI-MS/MS.
  • Water and swine feed by dual labeled time-resolved fluoroimmunoassay (TRFIA) using lanthanide ions-based fluorescent probes and HPLC equipped with ultraviolet (UV) detector.
  • Treated wastewater by direct injection (DI) combined with UHPLC coupled to quadrupole-linear ion trap analyser (QqLIT-MS/MS).

Biochem/physiol Actions

β2-adrenoceptor agonist

Disclaimer

sensitive to light

General description

Standard for Supelco MIP SPE cartridges. For more information request Supelco Literature T407075, T706019, T706030, T706020. Salbutamol is classified under the β-agonist group of chemicals which are known to possess powerful pharmacological activities.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark
GHS07

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Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Sens. 1B

Storage Class

11 - Combustible Solids

wgk

WGK 2

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK0230
BCBZ6220

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Fast determination of pesticides and other contaminants of emerging concern in treated wastewater using direct injection coupled to highly sensitive ultra-high performance liquid chromatography-tandem mass spectrometry.
Campos-Ma?as MC, et al.
Journal of Chromatography A, 1507(2), 84-94 (2017)
Comparison between liquid chromatography and supercritical fluid chromatography coupled to mass spectrometry for beta-agonists screening in feeding stuff.
Herpin L, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 1086(2), 130-137 (2018)
Determination of ractopamine and salbutamol in pig hair by liquid chromatography tandem mass spectrometry
Chang KC, et al.
Journal of food and drug analysis, 26(2), 725-730 (2018)
Simultaneous determination of ?-agonists clenbuterol and salbutamol in water and swine feed samples by dual-labeled time-resolved fluoroimmunoassay
Li M, et al.
Food Control, 73(2), 1039-1044 (2017)
Determination of the bioavailability of selected pharmaceutical residues in fish plasma using liquid chromatography coupled to tandem mass spectrometry.
Larabie SP, et al.
Journal of Chromatography A, 1522(2), 48-55 (2017)
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