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Home / Applications / Spectroscopic Evaluation of Color Development in Natural Colorants

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Spectroscopic Evaluation of Color Development in Natural Colorants

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April 22, 2025

Introduction

It is possible to easily numerically evaluate complex color changes for a sample using a color evaluation program.

Fig. 1 Butterfly pea flower and its herbal tea

Colorants are a type of food additive and are regulated by the laws and regulations of each country. In recent years, naturally derived additives have gained attention due to increasing consumer awareness of food safety. Butterfly pea extract (Figure 1) is a natural colorant with a vivid hue that changes with pH due to the presence of ternatin, a type of anthocyanin (Figure 2). Butterfly pea flower extract was added to the United States Food and Drug Administration (FDA) list of color additive certification exemptions published in 2021, and its use is expected to expand. In this report, we present the results of absorption measurements for butterfly pea extract at different pH using a JASCO UV-Visible spectrophotometer and objectively evaluate its color development using the JASCO color evaluation program.

Experimental

Sample

The components of dried butterfly pea petals were extracted into pure water, and ten samples with equal concentrations of butterfly pea extract were prepared. To adjust the pH, the same amount of either dilute hydrochloric acid, citric acid solution, sodium citrate buffer solution, sodium citrate solution, or sodium hydroxide (NaOH) solution was added. The concentration was adjusted using pure water. The pH of each solution was measured using a pH meter.

Fig. 2 Color of butterfly pea flower extracts with different pH values

Table 1   Added liquids and pH values for butterfly pea extract

SampleABCDEFGHIJ
Added LiquidDilute hydrochloric acidCitric acidCitric acidCitrate bufferPure waterCitrate bufferSodium citrateNaOHNaOHNaOH
pH0.62.32.94.05.06.07.17.89.812.1

System
Instrument:   V-750 UV-Visible spectrophotometer
Software:  VWCD-960 Color evaluation (color diagnosis) program

Parameters
Measurement range:  780 nm – 450 nm
Data interval:  0.2 nm
Bandwidth:  1.0 nm
Response:  0.06 sec
Scan speed:  400 nm/min
Path length:  10 mm

Keywords

Natural colorant, dye, butterfly pea, food additive, spectrophotometer, anthocyanin, pH, color evaluation

Results

Fig. 3 pH dependence of absorption spectrum of butterfly pea extract
Fig. 4 pH Dependence of absorbance (normalized to maximum value) at different wavelengths for butterfly pea petal extract

The absorption spectra of butterfly pea extracts with different pH values in the visible wavelength region are shown in Figure 3. The pH dependence of the intensity of different absorption bands is plotted in Figure 4. The absorption band intensity at around 400 nm significantly increases at pH 6.0 and above, while absorption at 545 nm decreases with increasing pH. the band intensity at 570 nm decreases at pH 5.0 and above, and absorption at 625 nm decreases at pH 7.1 and above. These changes correlate to changes in ternatin conformation (see appendix). In order to determine the effect of absorbance changes on the color of the solution color evaluation software was used to analyze the spectra.

Fig. 5 pH Dependence of color for butterfly pea petal extract

Figure 5 shows the results of a color analysis performed using the JASCO color evaluation program. Tracking the plot on the chromaticity diagram as the pH increases reveals that the direction of the color change shifts at around pH 4 due to decrease of the 570 nm absorption, and pH 7, where 625 nm absorption begins to decrease. Although the spectra for each pH exhibit complex changes, evaluation using a combination of chromaticity coordinates and color calculations allows the changes in the samples to be easily identified. The color evaluation program not only displays the measured spectra, but simultaneously shows color analysis results based on the specified color calculation conditions.

Conclusion

Our software effectively visualized the complex color changes of butterfly pea extract, which depend on pH. JASCO’s color evaluation program is ideal for assessing colorants and dyes that may exhibit intricate color variations. Plotting color coordinates on a chromaticity diagram allows an objective numerical representation of the coordinates while making color change trends instantly recognizable. Use of this system removes subjectivity in describing these color and removes complexity from spectral analysis.

Related Application Note: Combined Analysis of Thermochromic Materials: FT-IR Structural Analysis and UV-Vis Color Evaluation

References

1.The Food and Drug Administration, 21 CFR Part 73.69, Listing Of Color Additives Exempt From Certification; Butterfly Pea Flower Extracts, 2021

Acknowledgements
In preparing this report, we received invaluable support from Ms. Kei Okabe of Tokyo National College of Technology. I would like to take this opportunity to express my sincere gratitude.

Appendix – Conformational changes in ternatin due to pH

The relative intensity of different absorption bands for ternatin is dependent on the pH due to the coexistence of different molecular structures. Ternatin in butterfly pea flower extract has been reported to transition between four main structures depending on the pH, as shown in Figure 6. At around pH 1, it adopts the structure of a flavylium cation with absorption at 545 nm. As the pH increases, it shifts to two quinoid base structures, which are tautomers. At pH 4, the contribution of the structure that absorbs at 570 nm increases, and at pH 7, that of the structure that absorbs at 625 nm increases. As the pH increases from 8 to 9, the chalcone structure, which absorbs at about 400 nm, is formed.2,3) This relationship among pH, molecular structure, and absorption wavelength is in good agreement with the measurements in this report.

Fig. 6 Conformational change of ternatin

2.N. Terahara, et al. Tetrahedron letters, 31(20), 2921-2924 (1990). DOI: 10.1016/0040-4039(90)80185-O

3.B. Wiyantoko, Indonesian Journal of Chemical Analysis (IJCA), 3, 22-32 (2020). DOI: 10.20885/ijca.vol3.iss1.art4

This document has been prepared based on information available at the time of publication and is subject to revision without notice. Although the contents are checked with the utmost care, we do not guarantee their accuracy or completeness. JASCO Corporation assumes no responsibility or liability for any loss or damage incurred as a result of the use of any information contained in this document. Copyright and other intellectual property rights in this document remain the property of JASCO Corporation. Please do not attempt to copy, modify, redistribute, or sell etc. in whole or in part without prior written permission.
JASCO Application Note

Spectroscopic Evaluation of Color Development in Natural Colorants

Introduction

It is possible to easily numerically evaluate complex color changes for a sample using a color evaluation program.

Fig. 1 Butterfly pea flower and its herbal tea

Colorants are a type of food additive and are regulated by the laws and regulations of each country. In recent years, naturally derived additives have gained attention due to increasing consumer awareness of food safety. Butterfly pea extract (Figure 1) is a natural colorant with a vivid hue that changes with pH due to the presence of ternatin, a type of anthocyanin (Figure 2). Butterfly pea flower extract was added to the United States Food and Drug Administration (FDA) list of color additive certification exemptions published in 2021, and its use is expected to expand. In this report, we present the results of absorption measurements for butterfly pea extract at different pH using a JASCO UV-Visible spectrophotometer and objectively evaluate its color development using the JASCO color evaluation program.

Experimental

Sample

The components of dried butterfly pea petals were extracted into pure water, and ten samples with equal concentrations of butterfly pea extract were prepared. To adjust the pH, the same amount of either dilute hydrochloric acid, citric acid solution, sodium citrate buffer solution, sodium citrate solution, or sodium hydroxide (NaOH) solution was added. The concentration was adjusted using pure water. The pH of each solution was measured using a pH meter.

Fig. 2 Color of butterfly pea flower extracts with different pH values

Table 1   Added liquids and pH values for butterfly pea extract

SampleABCDEFGHIJ
Added LiquidDilute hydrochloric acidCitric acidCitric acidCitrate bufferPure waterCitrate bufferSodium citrateNaOHNaOHNaOH
pH0.62.32.94.05.06.07.17.89.812.1

System
Instrument:   V-750 UV-Visible spectrophotometer
Software:  VWCD-960 Color evaluation (color diagnosis) program

Parameters
Measurement range:  780 nm – 450 nm
Data interval:  0.2 nm
Bandwidth:  1.0 nm
Response:  0.06 sec
Scan speed:  400 nm/min
Path length:  10 mm

Results

Fig. 3 pH dependence of absorption spectrum of butterfly pea extract
Fig. 4 pH Dependence of absorbance (normalized to maximum value) at different wavelengths for butterfly pea petal extract

The absorption spectra of butterfly pea extracts with different pH values in the visible wavelength region are shown in Figure 3. The pH dependence of the intensity of different absorption bands is plotted in Figure 4. The absorption band intensity at around 400 nm significantly increases at pH 6.0 and above, while absorption at 545 nm decreases with increasing pH. the band intensity at 570 nm decreases at pH 5.0 and above, and absorption at 625 nm decreases at pH 7.1 and above. These changes correlate to changes in ternatin conformation (see appendix). In order to determine the effect of absorbance changes on the color of the solution color evaluation software was used to analyze the spectra.

Fig. 5 pH Dependence of color for butterfly pea petal extract

Figure 5 shows the results of a color analysis performed using the JASCO color evaluation program. Tracking the plot on the chromaticity diagram as the pH increases reveals that the direction of the color change shifts at around pH 4 due to decrease of the 570 nm absorption, and pH 7, where 625 nm absorption begins to decrease. Although the spectra for each pH exhibit complex changes, evaluation using a combination of chromaticity coordinates and color calculations allows the changes in the samples to be easily identified. The color evaluation program not only displays the measured spectra, but simultaneously shows color analysis results based on the specified color calculation conditions.

Conclusion

Our software effectively visualized the complex color changes of butterfly pea extract, which depend on pH. JASCO’s color evaluation program is ideal for assessing colorants and dyes that may exhibit intricate color variations. Plotting color coordinates on a chromaticity diagram allows an objective numerical representation of the coordinates while making color change trends instantly recognizable. Use of this system removes subjectivity in describing these color and removes complexity from spectral analysis.

Related Application Note: Combined Analysis of Thermochromic Materials: FT-IR Structural Analysis and UV-Vis Color Evaluation

Keywords

Natural colorant, dye, butterfly pea, food additive, spectrophotometer, anthocyanin, pH, color evaluation

References

1.The Food and Drug Administration, 21 CFR Part 73.69, Listing Of Color Additives Exempt From Certification; Butterfly Pea Flower Extracts, 2021

Acknowledgements
In preparing this report, we received invaluable support from Ms. Kei Okabe of Tokyo National College of Technology. I would like to take this opportunity to express my sincere gratitude.

Appendix – Conformational changes in ternatin due to pH

The relative intensity of different absorption bands for ternatin is dependent on the pH due to the coexistence of different molecular structures. Ternatin in butterfly pea flower extract has been reported to transition between four main structures depending on the pH, as shown in Figure 6. At around pH 1, it adopts the structure of a flavylium cation with absorption at 545 nm. As the pH increases, it shifts to two quinoid base structures, which are tautomers. At pH 4, the contribution of the structure that absorbs at 570 nm increases, and at pH 7, that of the structure that absorbs at 625 nm increases. As the pH increases from 8 to 9, the chalcone structure, which absorbs at about 400 nm, is formed.2,3) This relationship among pH, molecular structure, and absorption wavelength is in good agreement with the measurements in this report.

Fig. 6 Conformational change of ternatin

2.N. Terahara, et al. Tetrahedron letters, 31(20), 2921-2924 (1990). DOI: 10.1016/0040-4039(90)80185-O

3.B. Wiyantoko, Indonesian Journal of Chemical Analysis (IJCA), 3, 22-32 (2020). DOI: 10.20885/ijca.vol3.iss1.art4

This document has been prepared based on information available at the time of publication and is subject to revision without notice. Although the contents are checked with the utmost care, we do not guarantee their accuracy or completeness. JASCO Corporation assumes no responsibility or liability for any loss or damage incurred as a result of the use of any information contained in this document. Copyright and other intellectual property rights in this document remain the property of JASCO Corporation. Please do not attempt to copy, modify, redistribute, or sell etc. in whole or in part without prior written permission.
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