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. 2017 Mar 7;22(3):418. doi: 10.3390/molecules22030418

Table 1.

MRM parameters, chromatographic attributes, and quantitative response of stilbene compounds in standard samples.

Compound Formula Mass (Da) Precursor Ion (m/z) Product Ion (m/z) Collision Energy (eV) % Intensity Retention Time (Min–Max) trans/cis LOD (mg/L) LOQ (mg/L) Linearity b
Piceid C20H22O8 390.13 391.1 114.8 20 86.5 0.93–0.99/1.52–1.63 0.04 0.07 640
308.8 8 67.5
349.9 0 100
229.1 a 8 24.4
Resveratrol C14H12O3 228.08 229.09 107.1 a 24 100 1.85–1.99/2.55–2.65 0.12 0.22 800
91 a 24 45.7
135 a 8 80.9
165 a 28 35.6
Piceatannol C14H12O4 244.07 245.08 107.1 20 95.5 1.25–1.35/1.90–2.00 0.12 0.15 1600
135.1 12 100
152 36 11.6
181.1 24 38.7
ε-Viniferin C28H22O6 454.14 455.15 107.1 32 100 3.00–3.17/2.80–2.90 0.07 0.09 1777
215.1 20 75.0
349.1 16 38.5
199.1 24 32.0
Pteroestilbene C16H16O3 256,11 257.12 181 40 90.1 5.18–5.28/5.26–5.35 0.06 0.08 1000
133.1 12 100
91 28 58.5
165.1 40 72.2

a Transitions used for piceid analysis. b Ratio between the highest and lowest concentrations in linear range.