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MilliporeSigma

F8129

Sigma-Aldrich

Acid Fuchsin

Powder

Sinónimos:

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

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25 G
$93.80
50 G
$157.00
100 G
$292.00

$93.80


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25 G
$93.80
50 G
$157.00
100 G
$292.00

About This Item

Fórmula empírica (notación de Hill):
C20H17N3Na2O9S3
Número de CAS:
Peso molecular:
585.54
Colour Index Number:
42685
Beilstein/REAXYS Number:
4111656
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

$93.80


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Nombre del producto

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

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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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
Roberto Luongo et al.
The International journal of periodontics & restorative dentistry, 28(6), 551-557 (2009-01-17)
Platform switching is a concept recently introduced in implant dentistry. It is intended to reduce the crestal bone loss that is commonly found around implants exposed to the oral environment. The aim of this study was to examine biopsy specimens
Huan-Yan Xu et al.
Journal of hazardous materials, 175(1-3), 658-665 (2009-11-21)
The existence of 'electrostatic poles' on the schorl surface encouraged us to apply schorl for a TiO(2) support. TiO(2)/schorl composite photocatalyst was prepared and characterized by XRD, SEM and UV/DRS, and their photocatalytic activity was evaluated by discoloration of acid
Jong-Hwan Lee et al.
Neuroscience letters, 325(2), 129-133 (2002-06-05)
Ginsenosides are known to attenuate glutamate-induced cell injuries in vitro. We investigated the in vivo effect of ginsenosides on kainic acid (KA)-induced neurotoxicity in rat hippocampus using the methods of acid fuchsin (AF) staining and heat-shock protein-70 (HSP-70) immunoreactivity to

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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