1970
DOI: 10.1007/bf01225740
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D�termination spectrophotom�trique de l'analg�ne au moyen de chlorure de fer(III) et d'?,?'-dipyridyle

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Cited by 2 publications
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“…The reduction process of Fe( iii ) ions was followed by an increase in the concentration of Fe( ii ) ions, which form a colored complex with α,α′-dipyridyl. 66 The iron-reducing activity of diphenyl ethers 1–3 containing two hydroxyl groups was lower than the activity of BHT by more than 2 times. The iron-reducing activity of the monohydroxylated diphenyl ethers 4–7 was an order of magnitude lower than that of the dihydroxylated diphenyl ethers 1–3 (Table 2).…”
Section: Resultsmentioning
confidence: 96%
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“…The reduction process of Fe( iii ) ions was followed by an increase in the concentration of Fe( ii ) ions, which form a colored complex with α,α′-dipyridyl. 66 The iron-reducing activity of diphenyl ethers 1–3 containing two hydroxyl groups was lower than the activity of BHT by more than 2 times. The iron-reducing activity of the monohydroxylated diphenyl ethers 4–7 was an order of magnitude lower than that of the dihydroxylated diphenyl ethers 1–3 (Table 2).…”
Section: Resultsmentioning
confidence: 96%
“…The FRAP assay was adapted from previously described. 65,66 The reaction mixture (2 mL total volume) consisted of EtOH comparison of their spectroscopic data ( 1 H-, 13 C-NMR, HREI MS) with published values. [18][19][20][21]58 Reisolation of compounds 3-7 was described early.…”
Section: Ferric Reducing Antioxidant Power (Frap) Assaymentioning
confidence: 99%
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