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Table 1 Characteristic compounds of the dye materials in the Saltzman Collection

From: The analysis of the Saltzman Collection of Peruvian dyes by high performance liquid chromatography and ambient ionisation mass spectrometry

Dye source

Marker

Formula

Molecular mass

[M−H]−

[MH]+

[M+Na]+

References

Relbunium spp.

Purpurin

C14H8O5

256.037

255.029

257.045

279.027

Cardon [34]: 164, Dutra Moresi [33]

Xanthopurpurin

C14H8O4

240.042

239.034

241.050

263.032

Rubiadin/alizarin methyl ether

C15H10O4

254.058

253.050

255.066

277.048

Lucidin

C15H10O5

270.053

269.045

271.061

293.043

Munjistin

C15H8O6

284.032

283.024

285.040

307.022

Pseudopurpurin

C15H8O7

300.027

299.019

301.035

323.017

1-Methoxy-2-methylanthraquinone

C16H12O3

252.079

251.071

253.087

275.069

2-Methoxyanthraquinone or 1-hydroxy-2-methylanthraquinone

C15H10O3

238.063

237.055

239.071

261.053

Xanthopurpurin primeveroside

C25H26O13

534.137

533.129

535.145

557.127

Rubiadin primeveroside

C26H28O13

548.153

547.145

549.161

571.143

Lucidin primeveroside

C26H28O14

564.148

563.140

565.156

587.138

Galiosin (pseudopurpurin primeveroside)

C26H26O16

594.122

593.114

595.130

617.112

Dactylopius coccus

Carminic acid

C22H20O13

492.090

491.082

493.098

515.080

Cardon [34]:624, Wouters and Rosario-Chirinos [7], Stathopoulou et al. [37], Wouters and Verhecken [44]

Flavokermesic acid (laccaic acid D)

C16H10O7

314.043

313.035

315.051

337.033

Kermesic acid

C16H10O8

330.038

329.030

331.046

353.028

Flavokermesic acid glucopyranosides (dcII and dcofk)

C22H20O12

476.095

475.087

477.103

499.085

4-Aminocarminic acid (dcIII)

C22H21NO12

491.106

490.098

492.114

514.096

2-C-a/b-glucofuranoside of kermesic acid (dcIV and dcVII)

C22H20O13

492.090

491.082

493.098

515.080

Baccharis spp.

Apigenin

C15H10O5

270.053

269.045

271.061

293.043

Cardon [34]:233, Wouters and Rosario-Chirinos [7]; Akaike et al. [45]

Apigenin methyl ether

C16H12O5

284.068

283.060

285.076

307.058

Luteolin/kaempferol

C15H10O6

286.048

285.040

287.056

309.038

Luteolin methyl ether/trihydroxymethoxyflavone/(iso)kaempferide

C16H12O6

300.063

299.055

301.071

323.053

Kumatakenin/luteolin dimethyl ether

C17H14O6

314.079

313.071

315.087

337.069

Tetrahydroxymethoxyflavone/(iso)rhamnetin/3-methylquercetin

C16H12O7

316.058

315.050

317.066

339.048

Salvigenin

C18H16O6

328.095

327.087

329.103

351.085

Eupalitin/betuletol

C17H14O7

330.074

329.066

331.082

353.064

Eupatorin/cirsilineol

C18H16O7

344.090

343.082

345.098

367.080

Dimethylquercetagetin

C17H14O8

346.069

345.061

347.077

369.059

Sideritiflavone/jaceidin/centaureidin

C18H16O8

360.085

359.077

361.093

383.075

Quercetin-3-O-rutinoside (rutin)

C27H30O16

610.153

609.145

611.161

633.143

Di-O-caffeoylquinic acid

C25H24O12

516.127

515.119

517.135

539.117

 

O-caffeoyl-feruloylquinic acid

C26H26O12

530.142

529.135

531.150

553.132

 

Hypericum spp.

Dihydroxyxanthone

C13H8O4

228.042

227.034

229.050

251.032

Crockett et al. [39]

Quercetin

C15H10O7

302.043

301.035

303.051

325.033

Quercetin glucuronide

C21H18O13

487.075

486.067

488.083

510.065

Methylquercetin glucuronide

C22H20O13

492.090

491.082

493.098

515.080

Kageneckia spp.

Gallic acid

C7H6O5

170.022

169.014

171.030

193.012

No previous reports on K. lanceolata were found. K. oblongata is described by Cassels et al. [28]

Ursolic acid

C30H48O3

456.360

455.352

457.368

479.350