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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
Número MDL:
MFCD00941398
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329754035
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

100

Línea del producto

VETRANAL®

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

forensics and toxicology
pharmaceutical (small molecule)

formato

neat

cadena SMILES

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

Clave InChI

MMCDXJOMPMIKGP-UHFFFAOYSA-N

Descripción general

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

Aplicación

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.

Productos 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.

Información legal

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

Pictogramas

Exclamation mark
GHS07

Palabra de señalización

Warning

Frases de peligro

H315,H319,H335

Clasificaciones de peligro

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

Órganos de actuación

Respiratory system

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

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
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
Natalia Casado et al.
Talanta, 165, 223-230 (2017-02-06)
A SBA-15 type mesoporous silica was synthesized and bi-functionalized with octadecylsilane (C18) or octylsilane (C8), and sulfonic acid (SO

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