Research Article

Profiling Anthocyanins in Thai Purple Yams (Dioscorea alata L.)

Table 1

Mass spectrometric data and tentative identification of anthocyanins in the KKFCRC yam EtOH extracts.

Peak no.Retention time
(, min)
Area (%)Molecular ion precursor
[M]+ ().
MS2 fragment ion ()Tentative identificationMolecular formulaRemarks

126.781.25611611[M]+287Cyanidin-3-diglucosideC27H31O16
227.291.92773ā€”Cyanidin-3-diglucoside, 5-glucosideC33H41O21
331.171.09UnknownUnknownUnknownUnknown
433.231.81611611[M]+449, 287Cyanidin-3,5-diglucosideC27H31O16
538.444.46UnknownUnknownUnknownUnknown
639.412.79979979[M]+817, 449, 287Alatanin EC44H51O25Identified by [15]
740.404.59611611[M]+287Cyanidin-3-diglucosideC27H31O16
841.2611.13979979[M]+449, 287Alatanin E isomerC44H51O25Different fragment pattern from alatanin E identified by [15]
941.9016.1313471347[M]+979, 817, 449Alatanin BC61H71O34Identified by [14]
1042.9738.49817817[M]+449, 287Alatanin CC38H41O20Identified by [14]
1143.605.52787787[M]+287Alatanin G isomerC37H39O19Different fragment pattern from alatanin G identified by [15]
1243.845.7311851185[M]+817, 449Alatanin D isomerC55H61O29Different fragment pattern from alatanin D identified by [15]
1344.665.08831831[M]+Alatanin F isomerC39H43O20Different fragment pattern from alatanin F identified by [15]