Interpreted digital swatch

Alizarin crimson

Formula C₁₄H₈O₄Colour Index PR83 · lake of synthetic alizarin (1,2-dihydroxyanthraquinone)[1, 2, 4]Earliest recorded use 1868
8 eras11 artists12 colors

The first natural dye ever synthesised, and the pigment that ended a European agricultural industry within ten years of being invented. Alizarin crimson is deep, cool, transparent — and, despite a century of assuming otherwise, not permanent.

Origin

Alizarin is the principal colouring compound in madder root. In 1868 Carl Graebe and Carl Liebermann, working at the Berlin firm that would become BASF, determined its structure and synthesised it from anthracene, a coal-tar derivative; William Perkin arrived at a commercially viable route almost simultaneously in England, filing a patent one day after the German team. The consequence was immediate and brutal: madder was grown on tens of thousands of hectares in France, the Netherlands and the Levant, and within a decade that industry was gone. The synthetic product was cheaper, stronger, more consistent and free of the purpurin that made natural madder shift hue.[1, 2]

In art history

It appears in eight eras of this atlas, all of them after 1870, and it became the standard transparent red of modern painting — the crimson on virtually every twentieth-century palette, and the colour painters reach for to darken a red without dulling it or to glaze a shadow. It is also, historically, the first proof that a natural product could be manufactured more cheaply than it could be grown, a demonstration that reorganised the chemical industry and set the pattern for synthetic indigo, synthetic vanilla and everything after.

In the studio

It is intensely transparent and very strong, so it glazes beautifully and stains anything it touches. Mixed with white it gives clean cool pinks; mixed with ultramarine it gives the violets that were difficult before. It dries slowly in oil and forms a somewhat weak film, so it is best kept to upper layers and glazes. The serious issue is lightfastness. Alizarin was long sold and taught as permanent, and it is not: in thin applications and in tints it fades measurably, and testing since the mid-twentieth century has consistently rated it poor. A great many twentieth-century paintings have crimsons that are weaker than they were.[3, 4]

Afterlife

Most manufacturers now offer alizarin crimson hue, built from quinacridone, which is visually very close and genuinely lightfast, and some have discontinued the original entirely. The traditional pigment is still sold, largely because painters know the name and the handling, and it remains one of the clearest cases in the field of reputation outliving performance.

In different media

Oil
Transparent, and weakest exactly where it is most used: thin glazes and pale tints fade far faster than the full-strength colour.[3, 4]

Replacing alizarin crimson

Genuine alizarin crimson is PR83, a lake of synthetic alizarin. Its weakness shows exactly where it is used most, in thin glazes and pale tints. It is rated ASTM III (fair) for lightfastness, and in outdoor exposure tests published by Golden a 1:10 tint in oil changed more than twice as much as the full-strength colour. Winsor & Newton, which still sells it, rates its own alizarin crimson oil 'poor' for lightfastness.

Paints sold as 'permanent alizarin crimson' or 'alizarin permanent' are not one recipe, even within a single brand. Winsor & Newton's artists' oil version is anthraquinone red (PR177), its professional watercolour is perylene maroon (PR179), and its water-mixable oil combines PR179 with a quinacridone (PV19); Gamblin's Alizarin Permanent is PR177. Two tubes with the same name can hold different pigments, so the Colour Index code on the label is what to compare.

In the same Golden test, a PR177 tint changed about a tenth as much as the alizarin tint. None of the substitutes matches alizarin exactly in hue and transparency, which matters when retouching or matching an older painting. For new work they do what alizarin was asked to do, without the fading.[3, 4, 5, 6, 7, 8]

By Pigmentoria · Published · Updated

Sources

  1. Graebe, C. and Liebermann, C. (1868). Ueber Alizarin und Anthracen. Berichte der deutschen chemischen Gesellschaft 1, pp. 49–51. doi.org/10.1002/cber.18680010120
  2. Gettens, R. J. and Stout, G. L. (1942). Painting Materials: A Short Encyclopaedia. D. Van Nostrand, 1942; Dover reprint, 1966, s.v. Alizarin. archive.org/details/paintingmaterial0000gett
  3. Sands, S. (2016). Alizarin Crimson: Now You See It…. Just Paint (Golden Artist Colors). justpaint.org/alizarin-crimson-now-you-see-it/
  4. Winsor & Newton. Artists' Oil Colour: Alizarin Crimson (product data). winsornewton.com/products/artists-oil-colour-alizarin-crimson
  5. Winsor & Newton. Artists' Oil Colour: Permanent Alizarin Crimson (product data). winsornewton.com/products/artists-oil-colour-permanent-alizarin-crimson
  6. Winsor & Newton. Professional Watercolour: Permanent Alizarin Crimson (product data). winsornewton.com/products/professional-watercolour-permanent-alizarin-crimson
  7. Winsor & Newton. Artisan Water Mixable Oil: Permanent Alizarin Crimson (product data). winsornewton.com/products/artisan-water-mixable-oil-permanent-alizarin-crimson
  8. Gamblin Artists Colors. Alizarin Permanent (product data). gamblincolors.com/alizarin-permanent/

Lexicon: Lake

Others in this family: Vermilion · Red lead · Madder and the red lakes · Cadmium red

Where it appears

Every era and artist in this atlas whose palette includes this pigment. Links are reviewed by hand, and those that are not a named use of the pigment are marked.

Edvard MunchVampire red
FrankenthalerStain pink
RothkoSeagram red
Frida KahloMexican pink
Francis BaconCarcass red
Jenny SavilleScar tissue redContusion purple
Cecily BrownGesture red