Martius yellow

Martius yellow
Names
Preferred IUPAC name
2,4-Dinitronaphthalen-1-ol
Other names
2,4-Dinitronaphthol; Martinsgelb; C.I. 10315; Acid yellow 24
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.009.176 Edit this at Wikidata
EC Number
  • 210-093-1
MeSH C057508
UNII
  • InChI=1S/C10H6N2O5/c13-10-7-4-2-1-3-6(7)8(11(14)15)5-9(10)12(16)17/h1-5,13H X markN
    Key: FFRBMBIXVSCUFS-UHFFFAOYSA-N X markN
  • InChI=1/C10H6N2O5/c13-10-7-4-2-1-3-6(7)8(11(14)15)5-9(10)12(16)17/h1-5,13H
    Key: FFRBMBIXVSCUFS-UHFFFAOYAH
  • C1=CC=C2C(=C1)C(=CC(=C2O)[N+](=O)[O-])[N+](=O)[O-]
Properties
C10H6N2O5
Molar mass 234.167 g·mol−1
Appearance brownish-yellow powder
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Martius yellow is an organic compound with the formula C10H5(OH)(NO2)2. It is one of several isomers of dinitro-1-naphthol. It is prepared by nitration of 1-naphthol.

The compound was reported in the 1860's and then was briefly popular for dying wool. The dye was however not light-fast.

Martius yellow stains have been used to stain erythrocytes yellow so that they contrast well with red fibrin in trichrome staining methods such as Lendrum's Picro Mallory and Slidder's Martius, Scarlet and Blue (MSB). It can be combined with other small molecular weight yellow dyes to increase stain intensity.

References

  1. ↑ Raue, Roderich; Corbett, John F. (2000). "Nitro and Nitroso Dyes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_383. ISBN 3527306730.
  2. ↑ Maarten R. van Bommel and Matthijs de Keijzer (2025). "The Nitro Dyes". In Maarten R. van Bommel and Matthijs de Keijzer (ed.). Bright Colours from the Past: The History, Chemistry, Characterisation and Application of Synthetic Dyes Between 1856 and 1914. Springer, Cultural Heritage Science series. doi:10.1007/978-3-031-88664-5.