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. Author manuscript; available in PMC: 2014 Dec 15.
Published in final edited form as: Anal Biochem. 2013 Sep 11;443(2):222–231. doi: 10.1016/j.ab.2013.09.001

Table 2.

Spectroscopic and chromatographic properties of tryptophan and its major metabolites.

Analyte λmax of ex (nm) λmax of em (nm) λmax of abs (nm) Extinction coefficient (dm3 mol−1 cm−1) LOD (mol) S/N RT (min)
TRP 297 348 220 2.94 × 104 5.36 × 10−12 2.19 30.8
280 7.82 × 103 4.89 × 10−14 2.13
300sh 6.45 × 103
5-HT 297 348 220 3.25 × 104 5.84 × 10−12 2.55 7.91
280 5.51 × 103 1.13 × 10−13 2.06
300sh 4.68 × 103
5-HIAA 297 348 220 2.65 × 104 6.64 × 10−12 2.45 17.6
280 6.36 × 103 8.25 × 10−14(fl) 2.15
300sh 5.46 × 103
KYN 364 480 226 2.44 × 104 4.8 × 10−12 2.17 12.1
254 9.5 × 103 1.20 × 10−12 2.05
364 5.05 × 103
KYNA 330 390 216 2.95 × 104 3.28 × 10−12 2.14 21.6
242 3.92 × 104 1.13 × 10−13 2.18
330 6.79 × 103 2.24

TRP, tryptophan; 5-HT, serotonin; 5-HIAA, 5-hydroxyindoleacetic acid; KYN, kynurenine; KYNA, kynurenic acid; λmax of ex, wavelength of excitation maximum; λmax of em, wavelength of emission maximum; λmax of abs, wavelength of absorbance maximum; sh, shoulder; fl, by fluorescence; LOD, limit of detection represented in number of moles injected on the column observed for absorbance used for quantification of given analyte (top values) and fluorescence; S/N, signal-to-noise ratio; RT, retention time.