Structure via PubChem · Public domain (PubChem)
Gallocyanin
Sign in to saveAlso known as gallocyanine, Gallocyanine, Anthracene Blue SWGG, C.I. Mordant Blue 10, Brilliant Chrome Blue P, Alizarine Navy Blue AT, Solid Violet, Fast Violet
chemische Verbindung
In the Vinony graph
Within Vinony's link graph, Gallocyanin is referenced by 2 other articles, and connects out to International Standard Book Number, chemical formula and nucleic acids.
Vinony files it under Carboxylic acids, Chembox having GHS data and Chembox image size set.
Its subject is documented across 6 Wikipedia language editions.
Chemical data
- Formula
- C15H13ClN2O5
- Molecular weight
- 336.72 g/mol
- IUPAC name
- 7-(dimethylamino)-4-hydroxy-3-oxophenoxazin-10-ium-1-carboxylic acid chloride
- SMILES
- CN(C)C1=CC2=C(C=C1)[NH+]=C3C(=CC(=O)C(=C3O2)O)C(=O)O.[Cl-]
- InChIKey
- AQSOTOUQTVJNMY-UHFFFAOYSA-N
- Polar surface area
- 101 Ų
- H-bond donors
- 3
- H-bond acceptors
- 7
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
195 papers- Gallocyanin-chrome alum: II. Histochemistry and specificity.Stain technology · 1960
- Gallocyanin-indiumalum; electron stains I.Experimental cell research · 1953
- Gallocyanin chromalum as a nuclear stain in cytology. I. A cytophotometric comparison of the Husain-Watts Gallocyanin chromalum staining protocol with the Feulgen procedure.The Histochemical journal · 1991
- A simple method for the use of gallocyanin-chrome alum as an electron strain.Journal of microscopy · 1981
- Gallocyanin as a nuclear stain.Stain technology · 1947
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 336.051299196
- Has use
- dye
Show 2 more facts
- chemical formula
- C₁₅H₁₃ClN₂O₅
- canonical SMILES
- CN(C)C1=CC=C2C(=C1)[O+]=C3C(=N2)C(=CC(=C3O)O)C(=O)O.[Cl-]
Sources (2)
via Wikidata · CC0
Article · Deutsch
Gallocyanin ist eine chemische Verbindung aus der Gruppe der .
Abstract from DBpedia / Wikipedia · CC BY-SA
Connections
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