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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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About This Item

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

product name

Acid Fuchsin, used in tissue staining

Quality Level

form

powder

composition

Dye content, ~70%

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.

Application

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

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
Roberto Luongo et al.
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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
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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
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We report a facile approach to synthesizing and immobilizing zero-valent iron nanoparticles (ZVI NPs) onto polyelectrolyte (PE) multilayer-assembled electrospun polymer nanofibers for potential environmental applications. In this approach, negatively charged cellulose acetate (CA) nanofibers fabricated by electrospinning were assembled with

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