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N-Nitroso Sacubitril Impurity 1

N° de SZ CAT SZ-S020061
Número CAS NA
Mol.F. C18H18N2O2
Peso Molecular 294.4
Status de Fatura Custom Synthesis

Nome Químico: 5-([1,1'-Biphenyl]-4-ylmethyl)-3-methyl-1-nitrosopyrrolidin-2-one

Sorrisos: O=NN(C(CC1C)CC(C=C2)=CC=C2C3=CC=CC=C3)C1=O

Inchi: InChI=1S/C22H33NO8/c1-23(2)12-14-7-4-5-10-22(14,13-8-6-9-15(11-13)29-3)31-21-18(26)16(24)17(25)19(30-21)20(27)28/h6,8-9,11,14,16-19,21,24-26H,4-5,7,10,12H2,1-3H3,(H,27,28)/t14-,16+,17+,18-,19+,21+,22+/m1/s1

A liquid chromatographic method for separation of sacubitril–valsartan and their stereoisomeric impurities
Lu Zhou,  Liang Zou,  Lili Sun,  Hui Zhang,  Wenkai Hui and  Qiaogen Zou
Anal. Methods, 2018,10, 1046-1053
Quantification of potential genotoxic impurity in sacubitril/valsartan drug substance at ppm level by LC-MS/MS
Ravi Uppala, M.Arthanareeswari, S.Devikala,T.Pushpamalini, J. ArockiaSelvi
Materials Today: Proceedings Volume 14, Part 2, 2019, Pages 640-645
Experimental Design Approach in HPLC Method Development: Application for the Simultaneous Determination of Sacubitril and Valsartan in Presence of Their Impurities and Investigation of Degradation Kinetics
Bahia A. Moussa, Hanaa M. A. Hashem, Marianne A. Mahrouse & Sally T. Mahmoud
Chromatographia volume 81, pages139–156(2018)
Development and validation of a stability indicating UHPLC method for Sacubitril/Valsartan complex in the presence of impurities and degradation products
Pintu Prajapati, Dhara Bhayani, Priti Mehta.
J App Pharm Sci. 2020; 10(2): 97-107