Martius yellow

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Martius yellow
Martius yellow Structural Formula V1.svg
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 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 210-093-1
MeSH C057508
PubChem CID
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 mark.svgN
    Key: FFRBMBIXVSCUFS-UHFFFAOYSA-N X mark.svgN
  • 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
Appearancebrownish-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 that once was used to protect wool from moths. It is prepared by nitration of naphthol. [1]

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.