Gallocyanin

Last updated
Gallocyanin
Gallocyanin.svg
Names
IUPAC name
7-(Dimethylamino)-4-hydroxy-3-oxo-3H-phenoxazine-1-carboxylic acid
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.014.860
EC Number 216-345-7
PubChem CID
UNII
Properties
C15H12N2O5
Molar mass 300.270 g·mol−1
Hazards
GHS pictograms GHS-pictogram-exclam.svg
GHS signal word Warning
H302
P264, P270, P301+312, P330, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Gallocyanin is a chemical compound classified as a phenoxazine dye. In combination with certain metals, it is used to prepare gallocyanin stains that are used in identifying nucleic acids. [1]

Phenoxazine chemical compound

Phenoxazine is a heterocyclic compound. The structure of phenoxazine consists of an oxazine fused to two benzene rings. It occurs as the central core of a number of naturally occurring chemical compounds such as dactinomycin and litmus. The dyes Nile blue and Nile red are also based on a phenoxazine core.

Gallocyanin stain

The gallocyanin stain, also known as the gallocyanin-chromalum stain, is a stain of the oxazine group for total nucleic acids. It is prepared from gallocyanin and is an ideal method for numerous slides that need to be stained serially, equivalently, and reproducible.

Nucleic acid polymeric macromolecules

Nucleic acids are the biopolymers, or small biomolecules, essential to all known forms of life. The term nucleic acid is the overall name for DNA and RNA. They are composed of nucleotides, which are the monomers made of three components: a 5-carbon sugar, a phosphate group and a nitrogenous base. If the sugar is a compound ribose, the polymer is RNA ; if the sugar is derived from ribose as deoxyribose, the polymer is DNA.

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References

  1. C.K. Shah (1 January 1991). Modern Dictionary Cyto And Histo Chemistry. Discovery Publishing House. pp. 33–. ISBN   978-81-7141-151-1 . Retrieved 1 January 2013.