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32573

Supelco

Mabuterol hydrochloride

VETRANAL®, analytical standard

Sinónimos:

1-(4-Amino-3-chloro-5-trifluoromethylphenyl)-2-tert-butylaminoethanol hydrochloride

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About This Item

Fórmula empírica (notación de Hill):
C13H18ClF3N2O·HCl
Número de CAS:
54240-36-7
Peso molecular:
347.20
MDL number:
MFCD00941398
UNSPSC Code:
41116107
PubChem Substance ID:
329754035
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

VETRANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)

format

neat

SMILES string

Cl.CC(C)(C)NCC(O)c1cc(Cl)c(N)c(c1)C(F)(F)F

InChI

1S/C13H18ClF3N2O.ClH/c1-12(2,3)19-6-10(20)7-4-8(13(15,16)17)11(18)9(14)5-7;/h4-5,10,19-20H,6,18H2,1-3H3;1H

InChI key

MMCDXJOMPMIKGP-UHFFFAOYSA-N

General description

Mabuterol hydrochloride belongs to the class of β-agonist compounds that is extensively used for veterinary applications.

Application

Mabuterol hydrochloride may be used as an analytical reference standard for the determination of the analyte in royal jelly samples by ultra-performance liquid chromatography combined with quadrupole time-of-flight mass spectrometry (UPLC-QTOF-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCH0369
BCCG0282
BCCD4370
BCCB6620
BCBX0035

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Visite la Librería de documentos

Rapid screening and quantification of multi-class multi-residue veterinary drugs in royal jelly by ultra performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry.
Zhang Y, et al.
Food Control, 60, 667-676 (2016)
Shuyu Ouyang et al.
Toxicology in vitro : an international journal published in association with BIBRA, 77, 105251-105251 (2021-10-04)
β2-adrenoceptor (β2AR) agonists can stimulate skeletal muscle growth. Their illegal use in food-producing animals, human athletes and bodybuilders causes adverse health effects. In the present study, we developed 3D-QSAR models for predicting the activity of chemicals which can stimulate skeletal
Nurul Ain A Talib et al.
Molecules (Basel, Switzerland), 23(4) (2018-03-30)
Development of an immunoassay for clenbuterol (CLB) detection required an anti-CLB antibody as an important bioreceptor. In this study, we report our work on production and purification of a rabbit-derived polyclonal anti-CLB antibody. The antibody was then purified by nProtein
Kai Hu et al.
Food chemistry, 339, 128079-128079 (2020-11-07)
In this work, an efficient method for the determination of β-agonists and fluoroquinolones was established, based on a mixed-mode sorbent of magnetic sulfonated covalent organic framework composites. By coupling with HPLC-MS/MS, the main factors that affect the extraction procedure were
Nurul Ain A Talib et al.
Sensors (Basel, Switzerland), 18(12) (2018-12-14)
Clenbuterol (CLB) is an antibiotic and illegal growth promoter drug that has a long half-life and easily remains as residue and contaminates the animal-based food product that leads to various health problems. In this work, electrochemical immunosensor based on poly(3,4-ethylenedioxythiophene)/graphene
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