94972
Brombuterol hydrochloride
VETRANAL®, analytical standard
Synonym(s):
1-(4-Amino-3,5-dibromophenyl)-2-tert-butylaminoethanol hydrochloride
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C12H18Br2N2O · HCl
CAS Number:
Molecular Weight:
402.55
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
Recommended Products
grade
analytical standard
Quality Level
product line
VETRANAL®
Assay
≥99.0% (HPLC)
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
solid phase extraction (SPE): suitable
application(s)
forensics and toxicology
pharmaceutical (small molecule)
veterinary
format
neat
SMILES string
Cl.CC(C)(C)NCC(O)c1cc(Br)c(N)c(Br)c1
InChI
1S/C12H18Br2N2O.ClH/c1-12(2,3)16-6-10(17)7-4-8(13)11(15)9(14)5-7;/h4-5,10,16-17H,6,15H2,1-3H3;1H
InChI key
XGPFKIAOVSGRSY-UHFFFAOYSA-N
General description
Brombuterol hydrochloride is a beta-sympathomimetic compound with tocolytic, muscle-relaxant and bronchodilator properties and is widely used in therapy for their growth promoting and performance enhancement.
Application
Brombuterol hydrochloride may be used as an analytical reference standard for the quantification of the analyte in complex matrices and biological samples using different chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Recommended products
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
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
E Sangiorgi et al.
Journal of chromatography. B, Biomedical sciences and applications, 693(2), 468-478 (1997-06-06)
The multistep analytical procedure routinely applied in our laboratory for the detection of the aryl amine beta-agonists clenbuterol, mabuterol and mapenterol in bovine matrices has been extended to the analysis in urine samples of brombuterol, a new clenbuterol-like compound. In
Analysis of beta-agonist residues in bovine hair: Development of a UPLC?MS/MS method and stability study
Giannetti L, et al.
Journal of Chromatography. B, Biomedical Applications, 1036(3), 76-83 (2016)
Overcoming matrix effects in electrospray: Quantitation of ?-agonists in complex matrices by isotope dilution liquid chromatography?mass spectrometry using singly 13C-labeled analogues
Gonzalez-Antuna A, et al.
Journal of Chromatography A, 40-47 (2013)
C Montesissa et al.
Xenobiotica; the fate of foreign compounds in biological systems, 28(11), 1049-1060 (1999-01-08)
1. Clenbuterol (CBL) and bromobuterol (BBL) were both extensively metabolized by hepatic microsomes of swine to only one polar metabolite which was separated by hplc and purified to perform mass analysis. 2. LC-MIS analysis by direct infusion into an ion
Leslie C Dickson et al.
Journal of AOAC International, 88(1), 46-56 (2005-03-12)
A multiresidue method was developed and validated to screen bovine urine samples for 10 beta-2-adrenergic agonistic drugs--brombuterol, cimaterol, clenbuterol, clenpenterol, isoxsuprine, mabuterol, ractopamine, ritodrine, salbutamol, and tulobuterol--at the 2 microg/L level. The method is also quantitative in the range of
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service