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124508

Sigma-Aldrich

Gallocyanine

Dye content 90 %

Sinónimos:

7-Dimethylamino-4-hydroxy-3-oxo-phenoxazine-1-carboxylic acid

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About This Item

Fórmula empírica (notación de Hill):
C15H13ClN2O5
Número de CAS:
1562-85-2
Peso molecular:
336.73
Colour Index Number:
51030
Beilstein/REAXYS Number:
307454
EC Number:
216-345-7
MDL number:
MFCD00011926
UNSPSC Code:
12171500
PubChem Substance ID:
24847615
NACRES:
NA.47

form

powder

Quality Level

100

composition

Dye content, 90%

solubility

1 N NH4OH: 10 mg/mL

λmax

601 nm

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

[Cl-].C\[N+](C)=C1\C=CC2=Nc3c(OC2=C1)c(O)c(O)cc3C(O)=O

InChI

1S/C15H12N2O5.ClH/c1-17(2)7-3-4-9-11(5-7)22-14-12(16-9)8(15(20)21)6-10(18)13(14)19;/h3-6H,1-2H3,(H2-,16,18,19,20,21);1H

InChI key

ADAUKUOAOMLVSN-UHFFFAOYSA-N

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General description

Gallocyanine belongs to the oxazine class of dyes. It is synthesised from methanol solution of gallic acid in the presence of excess iodine. Gallocyanine is used to stain animal cells, mostly the nucleic acids. It also acts as a chelating agent and is used to determine bioactive compounds and several metal ions.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
SHBR3334
MKCG1506
MKBT6206V
10614CH
02813PX

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The Chemistry of Synthetic Dyes, 2, 783-783 (1952)
A R Villanueva et al.
Stain technology, 61(2), 83-88 (1986-03-01)
A gallocyanin method for demonstrating cement lines in thin, undecalcified sections of bone has been developed that is compatible with prestaining with osteochrome before plastic embedding. After sectioning at 5 microns on the Jung K heavy duty microtome, the sections
Quantitative changes in neuronal and glial cells in the suprachiasmatic nucleus as a function of the lighting conditions during weaning
Cambras T, et al.
Dev. Brain Res., 157(1), 27-33 (2005)
Friederike Zaubitzer et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 12(14), 3928-3934 (2006-03-08)
Indicator-displacement assays based on the organometallic complex [{Cp*RhCl2}2] (Cp*=pentamethylcyclopentadienyl) and the dye gallocyanine were used to sense amino sugars and aminoglycosides in buffered aqueous solution by conducting UV-visible spectroscopy. The data of three assays at pH 7.0, 8.0, and 9.0
E K Schulte et al.
The Histochemical journal, 24(6), 305-310 (1992-06-01)
For simultaneous cytophotometric measurement of DNA and RNA, the standardized Methyl Green-Pyronin Y technique is an obvious choice. It is, however, first necessary to correlate the uptake of Pyronin Y to the staining intensity of RNA. The material consisted of
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