1370101
USP
Lopinavir
United States Pharmacopeia (USP) Reference Standard
About This Item
biological source
synthetic
grade
pharmaceutical primary standard
Agency
USP/NF
API family
lopinavir
form
powder
packaging
pkg of 350 mg
manufacturer/tradename
USP
storage condition
protect from light
color
white to off-white
mp
255.2-260.6 °F (124—127°C)
solubility
chloroform: soluble
isopropanol: soluble
methanol: freely soluble
methylene chloride: freely soluble
water: practically insoluble
application(s)
pharmaceutical (small molecule)
format
neat
storage temp.
2-8°C
InChI
1S/C37H48N4O5/c1-25(2)34(41-20-12-19-38-37(41)45)36(44)39-30(21-28-15-7-5-8-16-28)23-32(42)31(22-29-17-9-6-10-18-29)40-33(43)24-46-35-26(3)13-11-14-27(35)4/h5-11,13-18,25,30-32,34,42H,12,19-24H2,1-4H3,(H,38,45)(H,39,44)(H,40,43)/t30-,31-,32-,34-/m0/s1
InChI key
KJHKTHWMRKYKJE-SUGCFTRWSA-N
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General description
Application
Analysis Note
Other Notes
related product
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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This application note illustrates how it is possible to set-up an assay method for Lopinavir and Ritonavir tablets.
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