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Key Documents

215945

Sigma-Aldrich

Pararosaniline acetate

Dye content 90 %

Synonym(s):

Basic Parafuchsin, Basic Red 9, Magenta O

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About This Item

Empirical Formula (Hill Notation):
C19H17N3 · C2H4O2
CAS Number:
Molecular Weight:
347.41
Colour Index Number:
42500
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

form

solid

Quality Level

composition

Dye content, 90%

mp

203 °C (dec.) (lit.)

solubility

95% ethanol: 0.1%

λmax

545 nm

ε (extinction coefficient)

≥11000 at 235-241 nm in ethanol: water (1:1) at 0.004%
≥16000 at 286-292 nm in ethanol: water (1:1) at 0.004%
≥78000 at 543-549 nm in ethanol: water (1:1) at 0.004%

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

CC(O)=O.Nc1ccc(cc1)C(\c2ccc(N)cc2)=C3\C=CC(=N)C=C3

InChI

1S/C19H17N3.C2H4O2/c20-16-7-1-13(2-8-16)19(14-3-9-17(21)10-4-14)15-5-11-18(22)12-6-15;1-2(3)4/h1-12,20H,21-22H2;1H3,(H,3,4)

InChI key

YIXIVOYGLPFDCY-UHFFFAOYSA-N

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Biochem/physiol Actions

Pararosaniline acetate is one of the components of basic fuchsin. It acts as a reversible, linear inhibitor of horse butyrylcholinesterase (BChE).

Other Notes

This is the pure, principal component of mixtures commonly referred to as Basic Fuchsin.

Legal Information

Magenta is a trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Health hazard

Signal Word

Warning

Hazard Statements

Hazard Classifications

Carc. 2

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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Michael D. Larra?aga, Richard J. Lewis, Robert A. Lewis
Hawley's Condensed Chemical Dictionary (2016)
Comparative effects of cationic triarylmethane, phenoxazine and phenothiazine dyes on horse serum butyrylcholinesterase.
Yucel YY
Archives of Biochemistry and Biophysics, 478, 201-205 (2008)
L Galassi
Biotechnic & histochemistry : official publication of the Biological Stain Commission, 68(3), 175-179 (1993-05-01)
Formation of crystals in Schiff reagents prepared from SO2 gas previously has been reported either soon after preparation, using high dye concentrations and heating, or after long periods of storage at room temperature. With the first type of procedure only
Qiuhua Wu et al.
Colloids and surfaces. B, Biointerfaces, 101, 210-214 (2012-09-27)
A superparamagnetic graphene-Fe(3)O(4) nanocomposite (G/Fe(3)O(4)) was synthesized by a facile one-pot solvothermal method. The nanocomposite G/Fe(3)O(4) prepared by the new method was firstly used as an adsorbent to remove dye for water pollution remediation. In comparison with G/Fe(3)O(4) prepared by
K A Crist et al.
Journal of cellular biochemistry. Supplement, 25, 49-56 (1996-01-01)
Image analysis of tissue biopsies for determination of DNA content as an early marker of neoplasia is hampered by the complexity of corrections necessary to dea with nuclear truncation and overlap in thin sections. The use of confocal laser scanning

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