One of the medicinal plants used to treat gastric infections is Limoniastrum feei (Plumbagenaceae). The plant is native to the southeast of Algeria (Saoura, region of Bechar) and Northern Africa [1][2][3]. The other uses of Limoniastrum feei are as an antibacterial for the treatment of bronchitis and for stomach infections [4,5]. LC separation followed by derivatization and detection by fluorometric methods, as described by Waridel et al. [6,7], allows a high specificity of detection.The elaboration of a more rapid detection method by LC-UV may be considered for a continuation of this work [8,9]. The liquid chromatography-UV method has been developed for the analysis and separation of saponin extracts from stems of Limoniastrum feei. The separation of saponins using Si-gel phase liquid chromatography and gradient elution with CHCl 3 : MeOH (65:35) as mobile phase has permitted good separation of all the peaks. The conditions of detection proposed for the separation are between 15 and 30 s. TLC analysis (CHCl 3 :MeOH, 65:35) revealed four constituent in the butanol fraction (yield 0.60%, R f 0.40, 0.48, 0.53, 0.58), six constituents in the ethyl acetate extract (yield 0.42%, R f 0.48, 0.58, 0.63, 0.66, 0.78, 0.86), and five constituents in the methylene chloride (DCM) extract (yield 0.31%, R f 0.6, 0.66, 0.76, 0.80, 0.88).Liquid chromatography coupled with UV has been used in phytochemical screening and analysis of the isolated constituent from extracts [10,11].The results obtained from the LC-UV system, retention times, yields, peak areas, and tailing factors, were analyzed The obtained values confirm that this method is suitable for routine analysis [8,9].The LC-UV analysis for butanolic extract gave eight constituents. Two fractions, 6 and 7, were isolated and purified by flash chromatography (Si-gel column), eluting with H 2 O /MeCN 75:35 and affording 65 mg of 6 and 90 mg of 7.In compound 6, the MS molecular ion was not observed, but two peaks were observed at m/z 282 and 234, coming from the retro Diels-Alder cleavage of the 12 Δ skeleton in oleanane derivatives. Its 13 C NMR spectrum showed 30 carbons and, in particular, two CH 2 OH, two CHOH, and an olefinic bond (145.7 and 122.7 ppm).The trisubstituted nature of the double bond was evidenced by the DEPT spectrum and the presence of one olefinic proton as an undefined triplet at 5.25 ppm in the 1 H NMR spectrum. The DEPT experiment revealed that the 32 carbons consisted of 7 CH 3 , 11 CH 2 , 6 CH, and 8 quaternary carbons.The six methyl groups have to be located at quaternary carbons since they resonate as singlets in the 1 H NMR spectrum. The remaining primary alcoholic function has to be placed in position 30 on the basis of a comparison with the 13 C NMR data available in the literature [12,13]. Therefore, compound 6 is 2α,3β,23-trihydroxy-30-acetylolean-12-ene.