2016
DOI: 10.1039/c6ra02912d
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Preparation of glycerol monostearate from glycerol carbonate and stearic acid

Abstract: A new two-step procedure prepares glycerol monostearate from glycerol carbonate and stearic acid.

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Cited by 28 publications
(17 citation statements)
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“…Figure 3a shows the results of the FT-IR analysis for ceftriaxone sodium, Glycerol Monostearate, and nano-carriers containing ceftriaxone sodium. The FT-IR analysis of ceftriaxone sodium exhibits a band at 3444.63 cm − 1 , which can be attributed [26]. As shown in Fig.…”
Section: Characterization Of Optimized Structurementioning
confidence: 87%
“…Figure 3a shows the results of the FT-IR analysis for ceftriaxone sodium, Glycerol Monostearate, and nano-carriers containing ceftriaxone sodium. The FT-IR analysis of ceftriaxone sodium exhibits a band at 3444.63 cm − 1 , which can be attributed [26]. As shown in Fig.…”
Section: Characterization Of Optimized Structurementioning
confidence: 87%
“…The main peaks related to the GMS structure were observed at 3314 cm À1 (O-H), 2916 cm À1 and 2849 cm À1 (C-H), 1730 cm À1 (C]O), 1180 cm À1 and 1047 cm À1 (C-O). 45 The principle peaks of melatonin were observed at 3303 cm À1 (N-H), 1629 cm À1 (C]O), 1555 cm À1 (C-O) and 1212 cm À1 (C-N). 46 The NLC spectrum is comparable to that of GMS, which could be due to high lipid content compared to the amount of drug.…”
Section: Particle Size and Morphology Tem (mentioning
confidence: 96%
“…Repeated column chromatography for the n-BuOH Fr of M. verticillata aerial parts led to the isolation of four glycerides (1-4), which were identified as (2S)-1-O-palmitoyl glyceride [24], (2S)-1-O-stearoyl glyceride [25], (2S)-1-Olinolenoyl glyceride [26], and (2S)-1,2-di-O-linoleoyl glyceride [27], respectively, based on NMR, IR, FAB-MS, GC-MS, and FAB-MS analyses in addition to comparison of the data with those in literatures (Table 1).…”
Section: Resultsmentioning
confidence: 99%