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Supelco

Brombuterol hydrochloride

VETRANAL®, analytical standard

Sinônimo(s):

1-(4-Amino-3,5-dibromophenyl)-2-tert-butylaminoethanol hydrochloride

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About This Item

Fórmula empírica (Notação de Hill):
C12H18Br2N2O · HCl
Número CAS:
Peso molecular:
402.55
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

linha de produto

VETRANAL®

Ensaio

≥99.0% (HPLC)

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable
solid phase extraction (SPE): suitable

aplicação(ões)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

formato

neat

cadeia de caracteres SMILES

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

chave InChI

XGPFKIAOVSGRSY-UHFFFAOYSA-N

Descrição geral

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.

Aplicação

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.

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Produtos recomendados

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.

Informações legais

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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Certificados de análise (COA)

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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
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)
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)
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
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

Artigos

Using an Ascentis® Express F5 HPLC column, this study separates 11 β-agonists in pork by LC-MS/MS in under 8 minutes with excellent recovery and precision.

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