Alizarin
From Wikipedia, the free encyclopedia
| Alizarin | |
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| IUPAC name | 1,2-dihydroxy-9,10-anthracenedione |
| Other names | 1,2-dihydroxyanthraquinone, Turkey red, mordant red 11, alizarin B, alizarin red, 9,10-anthracenedione |
| Identifiers | |
| CAS number | [72-48-0] |
| SMILES | Oc2c(O)c1C(=O)c3c(C(=O)c1cc2)cccc3 |
| Properties | |
| Molecular formula | C14H8O4 |
| Molar mass | 240.21 g/mol |
| Appearance | orange-red crystals or powder |
| Melting point |
279 - 283 °C |
| Boiling point |
430 °C |
| Solubility in water | ? g/100 ml (?°C) |
| Hazards | |
| MSDS | External MSDS |
| R-phrases | R36 R37 R38 |
| S-phrases | S26 S36 |
| Related compounds | |
| Related compounds | anthraquinone, anthracene |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
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Alizarin is an organic compound that is historically important as a prominent dye. It is an anthraquinone originally derived from the root of the madder plant. In 1869, it became the first natural pigment to be duplicated synthetically.[1] Alizarin is also the name for a variety of related dyes, such as "Alizarine Cyanine Green G" and "Alizarine Brilliant Blue R."
The word alizarin derives from the Arabic al-usara, juice.[2]
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[edit] History
Madder has been cultivated as a dyestuff since antiquity in central Asia and Egypt, where it was grown as early as 1500 BC. Cloth dyed with madder root pigment was found in the tomb of the Pharaoh Tutankhamun and in the ruins of Pompeii and ancient Corinth. In the Middle Ages, Charlemagne encouraged madder cultivation. It grew well in the sandy soils of the Netherlands and became an important part of the local economy.
By 1804, the English dye maker George Field[3] had refined the technique to lake madder by treating it with alum, and an alkali,[4] that converts the water-soluble madder extract into a solid, insoluble pigment. This resulting madder lake has a longer-lasting color, and can be used more versatilely, for example by blending it into a paint. Over the following years, it was found that other metal salts, including those containing iron, tin, and chromium, could be use in place of alum to give madder-based pigments of various other colors. This general method of preparing lakes has been known for centuries.[5]
In 1826, the French chemist Pierre-Jean Robiquet found that madder root contained two colorants, the red alizarin and the more rapidly fading purpurin. The alizarin component became the first natural dye to be synthetically duplicated in 1868 when the German chemists Carl Graebe and Carl Liebermann, working for BASF, found a way to produce it from anthracene. About the same time, the English dye chemist William Henry Perkin independently discovered the same synthesis, although the BASF group filed their patent before Perkin by only one day.
The synthetic alizarin could be produced for a fraction of the cost of the natural product, and the market for madder collapsed virtually overnight. The principal synthesis entailed oxidation of anthraquinone-2-sulfonic acid with sodium nitrate in concentrated sodium hydroxide. Alizarin itself has been in turn largely replaced today by the more light-resistant quinacridone pigments developed at DuPont in 1958.
[edit] Applications
Alizarin red is used in a biochemical assay to determine, quantitatively by colorimetry, the presence of calcific deposition by cells of an osteogenic lineage. As such it is an early stage marker (days 10-16 of in vitro culture) of matrix mineralisation, a crucial step towards the formation of calcified extracellular matrix associated with true bone.
In clinical practice it is also used to stain synovial fluid to assess for basic calcium phosphate crystals.
[edit] Alizarin Crimson
| Alizarin Crimson | ||
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| Hex triplet | #E32636 | |
| B | (r, g, b) | (227, 38, 54) |
| HSV | (h, s, v) | (348°, 90%, 77%) |
| Source | BF2S Color Guide | |
| B: Normalized to [0–255] (byte) |
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At right is displayed the color alizarin crimson.
[edit] In popular culture
The color is one of several mentioned in the 1967 song "Wear Your Love Like Heaven" by Donovan.
[edit] References
- ^ Hans-Samuel Bien, Josef Stawitz, Klaus Wunderlich “Anthraquinone Dyes and Intermediates” in Ullmann’s Encyclopedia of Industrial Chemistry 2005 Wiley-VCH, Weinheim: 2005. doi:10.1002/14356007.a02 355.
- ^ alizarin. Dictionary.com. Dictionary.com Unabridged (v 1.1). Random House, Inc. http://dictionary.reference.com/browse/alizarin (accessed: January 02, 2007).
- ^ Field's notes are held at the Courtauld Institute of Art. See: http://www.aim25.ac.uk/cgi-bin/search2?coll_id=4107&inst_id=2 (accessed: 2007/09/05)
- ^ Winsor Newton's madder pigment is made according to his process. See http://www.winsornewton.com/artnews/EN/artnewsletterA4_english03_2002.pdf page 6. (accessed: 2007/09/03). Note that Henry Charles Newton, founder of Winsor Newton, was his assistant and friend.
- ^ Daniel V. Thompson - The Materials and Techniques of Medieval Painting - Dover - pp115-124. ISBN 0-486-20327-1
