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A Microscale Synthesis of Mauve

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Cleveland State University, Department of Chemistry, Euclid Avenue at East 24th Street, Cleveland, OH 44115
Cite this: J. Chem. Educ. 1998, 75, 6, 769
Publication Date (Web):June 1, 1998
https://doi.org/10.1021/ed075p769.2

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    Abstract

    We have reproduced Perkin's synthesis of mauve and have scaled it down to microscale levels. As such, we present a synthesis of mauve that can be performed in a microscale organic chemistry laboratory.

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    Cited By

    This article is cited by 12 publications.

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    3. Corina E. Rogge and Anikó Bezur . An Investigation into the Creation, Stability, and X-ray Fluorescence Analysis of Early Photographic Processes: An Upper-Level Undergraduate Laboratory. Journal of Chemical Education 2012, 89 (3) , 397-400. https://doi.org/10.1021/ed101185d
    4. Dotse Selali Chormey, Buse Tuğba Zaman, Esra Maltepe, Çağdaş Büyükpınar, Ayşe Evrim Bulgurcuoğlu, Fatma Turak, Fatih Ahmet Erulaş, Sezgin Bakırdere. Simultaneous Determination of Harmful Aromatic Amine Products of Azo Dyes by Gas Chromatography–Mass Spectrometry. Journal of Analytical Chemistry 2020, 75 (10) , 1330-1334. https://doi.org/10.1134/S1061934820100044
    5. Tânia F. G. G. Cova, Alberto A. C. C. Pais, J. Sérgio Seixas de Melo. Reconstructing the historical synthesis of mauveine from Perkin and Caro: procedure and details. Scientific Reports 2017, 7 (1) https://doi.org/10.1038/s41598-017-07239-z
    6. M. John Plater, Andrea Raab. Who Made Mauveine First: Runge, Fritsche, Beissenhirtz or Perkin?. Journal of Chemical Research 2016, 40 (12) , 758-762. https://doi.org/10.3184/174751916X14792902529027
    7. M. John Plater, Andrea Raab. Mauveine and the Mauve Shade Six Pence Stamp. Journal of Chemical Research 2016, 40 (11) , 648-651. https://doi.org/10.3184/174751916X14725625519561
    8. M. V. Cañamares, D. A. Reagan, J. R. Lombardi, M. Leona. TLC‐SERS of mauve, the first synthetic dye. Journal of Raman Spectroscopy 2014, 45 (11-12) , 1147-1152. https://doi.org/10.1002/jrs.4508
    9. M. John Plater. A Synthesis of Pseudo-Mauveine and a Homologue. Journal of Chemical Research 2011, 35 (5) , 304-309. https://doi.org/10.3184/174751911X13052165053977
    10. J. Seixas de Melo, S. Takato, M. Sousa, M. J. Melo, A. J. Parola. Revisiting Perkin's dye(s): the spectroscopy and photophysics of two new mauveine compounds (B2 and C). Chemical Communications 2007, 22 (25) , 2624. https://doi.org/10.1039/b618926a
    11. Teodoro S. Kaufman, Edmundo A. Rúveda. Die Jagd auf Chinin: Etappenerfolge und Gesamtsiege. Angewandte Chemie 2005, 117 (6) , 876-907. https://doi.org/10.1002/ange.200400663
    12. Teodoro S. Kaufman, Edmundo A. Rúveda. The Quest for Quinine: Those Who Won the Battles and Those Who Won the War. Angewandte Chemie International Edition 2005, 44 (6) , 854-885. https://doi.org/10.1002/anie.200400663

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