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Lopinavir EP Impurity F

Lopinavir EP Impurity F

Product Description
CAT No.
ALN-L008007
CAS No.
NA
Mol. F.
C29H34N2O4
Mol. Wt.
474.6
Stock
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RFQ
Chemical Name : N-[(1S,2S,4S)-1-Benzyl-4-(formylamino)-2-hydroxy-5-phenylpentyl]-2-(2,6-dimethylphenoxy)acetamide (as per EP); 2-(2,6-Dimethylphenoxy)-N-[(2S,3S,5S)-5-formamido-3-hydroxy-1,6-diphenylhexan-2-yl]acetamide (as per USP)
Smiles : O=C(COC1=C(C)C=CC=C1C)N[C@](CC2=CC=CC=C2)([H])[C@]([H])(C[C@](NC=O)([H])CC3=CC=CC=C3)O
Inchi : InChI=1S/C28H34N2O3/c1-20-10-9-11-21(2)28(20)33-19-27(32)30-25(17-23-14-7-4-8-15-23)26(31)18-24(29)16-22-12-5-3-6-13-22/h3-15,24-26,31H,16-19,29H2,1-2H3,(H,30,32)/t24-,25-,26-/m0/s1
Synonym : Lopinavir N-Formylphenoxyacetamide (USP)

Stability indicative and cost effective creation and validation of analytical method of Lopinavir and Rilpivirine by high performance liquid chromatography

By Srinivas, L.; Jain, NeelunFrom International Journal of Research in Pharmaceutical Sciences (Madurai, India) (2021), 12(1), 786-792

Analytical methods development & validation for simultaneous estimation of lopinavir & ritonavir in pharmaceutical formulation by simultaneous equation method using UV spectrophotometry

By Jadhav, Sarika R.; Alhat, Hemant P.; Joshi, Suhas – From International Research Journal of Pharmacy (2018), 9(8), 57-62

Development and validation of forced degradation studies of lopinavir using RP-HPLC and characterization of degradants by LC-MS/MS

By Bhavyasri, Khagga; Balaram, V. Murali; Nageswarao, R.; Rambabu, D.; Ajitha, M. – From International Journal of Chemical Sciences (2015), 13(1), 551-562

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