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F8129

Sigma-Aldrich

Acid Fuchsin

Powder

Synonym(s):

Acid Violet 19, Fuchsin S, Fuchsin acid, Rubine S

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25 G
€102.00
50 G
€188.00
100 G
€340.00

€102.00


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25 G
€102.00
50 G
€188.00
100 G
€340.00

About This Item

Empirical Formula (Hill Notation):
C20H17N3Na2O9S3
CAS Number:
Molecular Weight:
585.54
Colour Index Number:
42685
Beilstein:
4111656
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

€102.00


Please contact Customer Service for Availability

Request a Bulk Order

Product Name

Acid Fuchsin, used in tissue staining

Quality Level

form

powder

composition

Dye content, ~70%

technique(s)

microbe id | staining: suitable

color

blue-green

solubility

H2O: 1 mg/mL

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

[Na+].[Na+].Cc1cc(cc(c1N)S([O-])(=O)=O)\C(c2ccc(N)c(c2)S([O-])(=O)=O)=C3/C=CC(=N)C(=C3)S(O)(=O)=O

InChI

1S/C20H19N3O9S3.2Na/c1-10-6-13(9-18(20(10)23)35(30,31)32)19(11-2-4-14(21)16(7-11)33(24,25)26)12-3-5-15(22)17(8-12)34(27,28)29;;/h2-9,23H,21-22H2,1H3,(H,24,25,26)(H,27,28,29)(H,30,31,32);;/q;2*+1/p-2

InChI key

WZRZTHMJPHPAMU-UHFFFAOYSA-L

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General description

Acid Fuchsin is mainly used as a diachrome and is part of the connective tissue stains. It also works as a pH indicator.[1]

Application

Acid Fuchsin has been used in tissue sections for Masson′s trichrome staining.[2] It has been used as a marker to trace ingestion of solutions by green peach aphids.[3]

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Toshihiro Umebayashi et al.
Tree physiology, 27(7), 993-999 (2007-04-04)
To elucidate the water-conducting pathways in living trees by the dye injection method, suitable sample preparation procedures are needed. We evaluated quantitatively the properties and concentrations of three dyes (acid fuchsin, basic fuchsin and safranin) widely used for this purpose
G Vinitha et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 69(4), 1160-1164 (2007-08-08)
Solid-state dye-doped polymers are attractive alternative to the conventional liquid dye solutions. In this paper, nonlinear properties of the dye Acid Fuchsin has been studied. The third-order nonlinear optical properties of Acid Fuchsin dye in 1-butanol and dye-doped polymer film
Andrea Zsombok et al.
Journal of neuroscience methods, 142(1), 145-152 (2005-01-18)
By means of a condenser discharge electric shock paradigm, "dark" (compacted) granule neurons were momentarily produced in the hippocampal dentate gyri of rats, which were sacrificed either immediately or following survival periods ranging from 1h to 30 days. Except for
Fanling Meng et al.
Journal of molecular biology, 400(3), 555-566 (2010-05-11)
Islet amyloid polypeptide (IAPP), also known as amylin, is responsible for amyloid formation in type 2 diabetes. The formation of islet amyloid is believed to contribute to the pathology of the disease by killing beta-cells, and it may also contribute
Hongtao Huang et al.
Nanotechnology, 23(10), 105502-105502 (2012-03-01)
Zn-doped SnO(2) nanorods have been prepared by a simple hydrothermal method on a large scale. The as-prepared samples were characterized by x-ray powder diffraction, scanning electron microscope, transmission electron microscope, energy dispersive spectrometer, x-ray photoelectron spectroscopy, UV-vis absorption spectra and

Questions

  1. Quiero hacer una tinción de AFOG en tejido de pez cebra. Dispongo de los productos F8129 y O7252. Ambos productos vienen en polvo, ¿en qué tengo que diluirlos y en qué proporción tengo que mezclarlos?, ¿tenéis un protocolo?, dispongo del procedure HT15.

    1 answer
    1. Unfortunately, there are no available solutions, kits, or instructions for preparing an Acid Fuchsin Orange G (AFOG) stain.

      Please review the publication below that may be helpful:
      Poss KD, Wilson LG, Keating MT: Heart regeneration in zebrafish. Science. 2002, 298: 2188-90. 10.1126/science.1077857.

      Helpful?

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