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Atenolol R-Isomer

SZ CAT No SZ-A035010
CAS No 56715-13-0
Mol.F. C14H22N2O3
Mol.Wt. 266.3
Inv. Status Custom Synthesis


Chemical Name: (+)-2-[4-[(2R)-2-Hydroxy-3-[(1-methylethyl)amino]propoxy] phenyl] acetamide

Smiles: O=C(O)CC1=CC=C(OC[C@H](O)CNC(C)C)C=C1

Inchi: InChI=1/C14H20N2O2/c1-11(2)16-9-13(17)10-18-14-5-3-12(4-6-14)7-8-15/h3-6,11,13,16-17H,7,9-10H2,1-2H3

The assay and resolution of the beta-blocker atenolol from its related impurities in a tablet pharmaceutical dosage form
Zen pawlak* and Brian j. clark
Journal of Pharmaceutical & Biomedical Analysis Vol. 10, No. 5, pp. 329-334,1992
 
Removal of Atenolol and Isoproturon in Aqueous Solutions by Adsorption in a Fixed-Bed Column
JoséLuis Sotelo, Gabriel Ovejero, Araceli Rodríguez, Silvia Á lvarez, and Juan García
Ind. Eng. Chem. Res. 2012, 51, 5045−5055
 
A simple, selective, and sensitive gas chromatography-mass spectrometry method for the analysis of five process-related impurities in atenolol bulk drug and capsule formulations
Ambavaram Vijaya Bhaskar Reddy  Zulkifli Yusop  Jafariah Jaafar  Azmi Bin Aris  Zaiton Abdul Majid
JSS Volume 40, Issue 15 Pages: 3016-3182 August 2017
 
A Sensitive and Selective GC–MS Method for Analysis of Process-Related Genotoxic Impurities in Atenolol
Yogeshwar Reddy Mamilla1,3,&, Kista Reddy Chetyala3 , Ramesh Venna2 , Raju Gajjela2 , Kishore Katragadda1 , Saravanan Govindasamy1 , Suryanarayana Mulukutla1 , Debashish Datta
Chromatographia 2010, 71, 733–736
 
Development and validation of liquid chromatographic method for atenolol and its related substance
Nandini R. Pai* and Swapnali Suhas Patil
Der Pharmacia Sinica, 2013, 4(2):76-84