RAC ALBUTEROL-D9
RAC ALBUTEROL-D9 Basic information
- Product Name:
- RAC ALBUTEROL-D9
- Synonyms:
-
- RAC ALBUTEROL-D9
- a1-[[(1,1-Dimethylethyl)amino]methyl]-4-hydroxy-1,3-benzenedimethanol-d9
- Salbutamol-d9
- (±)-2-(tert-Butyl-d9-amino)-1-[4-hydroxy-3-(hydroxymethyl)phenyl]ethanol acetate salt
- Albuterol-(tert-butyl-d9) acetate
- α1-[[(1,1-DiMethylethyl)aMino]Methyl]-4-hydroxy-1,3-benzenediMethanol-d9
- SalbutaMol-D9 acetate(Albuterol-D9 acetate)
- Salbutamol-(tert-butyl-d9) acetate
- CAS:
- 1173021-73-2
- MF:
- C13H12D9NO3
- MW:
- 248.37
- Product Categories:
-
- Inhibitors
- Intermediates & Fine Chemicals
- Isotope Labeled Compounds
- Pharmaceuticals
- All Inhibitors
- Aromatics
- Isotope Labelled Compounds
- Mol File:
- 1173021-73-2.mol
RAC ALBUTEROL-D9 Chemical Properties
- Melting point:
- 142-146°C
- storage temp.
- -20°C Freezer
- solubility
- Methanol (Slightly), Water (Slightly)
- form
- Solid
- color
- White to Yellow
RAC ALBUTEROL-D9 Usage And Synthesis
Description
Salbutamol-d9 is intended for use as an internal standard for the quantification of salbutamol (Item Nos. 21003 | 23991) by GC- or LC-MS. Salbutamol is an agonist of the β2-adrenergic receptor (β2-AR; Kd = 759 nM in a radioligand binding assay using CHO cells expressing the human receptor). It is selective for β2-ARs over β1- and β3-ARs (Kds = 46.8 and 21.9 μM, respectively). Salbutamol (25-50 μg/kg, i.v.) reduces acetylcholine-induced bronchospasm in anesthetized guinea pigs. It also reduces response of bronchial muscle to efferent vagal stimulation in anesthetized cats and dogs when administered at doses ranging from 1 to 2.5 and 10 to 20 μg/kg, respectively. Nebulized salbutamol reduces transpulmonary pressure in recurrent airway obstruction-affected horses (EC50 = 39.7 μg). Formulations containing salbutamol have been used in the treatment of asthma and chronic obstructive pulmonary disease (COPD).
Chemical Properties
Off-White to Pale Yellow Solid
Uses
A labeled ?-adrenoceptor agonist
Uses
RAC ALBUTEROL-D9 is a labelled β2-adrenoceptor agonist,it is intended for use as an internal standard for the quantification of Albuterol by GC- or LC-mass spectrometry.
Uses
A labelled β2-adrenoceptor agonist. Bronchodilator; tocolytic.
References
[1] CHRISTOPHER KERN. Synthesis and Pharmacological Characterization of β2-Adrenergic Agonist Enantiomers: Zilpaterol[J]. Journal of Medicinal Chemistry, 2009, 52 6: 1773-1777. DOI: 10.1021/jm801211c
[2] BAKER J G. The selectivity of β-adrenoceptor antagonists at the human β1, β2 and β3 adrenoceptors[J]. British Journal of Pharmacology, 2009, 144 3: 317-322. DOI: 10.1038/sj.bjp.0706048
[3] VALERIE A. CULLUM. Salbutamol: a new, selective β-adrenoceptive receptor stimulant[J]. British Journal of Pharmacology, 1969, 35 1: 141-151. DOI: 10.1111/j.1476-5381.1969.tb07975.x
[4] M.G. ARROYO. Efficacy of Inhaled Levalbuterol Compared to Albuterol in Horses with Recurrent Airway Obstruction[J]. Journal of Veterinary Internal Medicine, 2016, 30 4: 1333-1337. DOI: 10.1111/jvim.14320
RAC ALBUTEROL-D9Supplier
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 021-50135380
- shchemsky@sina.com
- Tel
- +1.415.685.4395
- enquiry@clearsynth.com
- Tel
- 15374522761
- 3003392093@qq.com
- Tel
- 0755-0755-28967200-8062 13631290199
- wxf@sungening.com