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Merck
CN

P1528

Pararosaniline hydrochloride

certified by the BSC

Synonym(s):

Basic Fuchsin, Basic Parafuchsin, Basic Red 9, Magenta™ O, Parafuchsin hydrochloride, Paramagenta hydrochloride, Pararosaniline chloride

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About This Item

Linear Formula:
C19H18N3Cl
CAS Number:
569-61-9
Molecular Weight:
323.82
EC Number:
209-321-2
PubChem Substance ID:
24898215
UNSPSC Code:
12171500
Beilstein/REAXYS Number:
4164603
Colour Index Number:
42500
MDL number:
MFCD00001657

Key Documents

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InChI

1S/C19H17N3.ClH/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;/h1-12,20H,21-22H2;1H

InChI key

JUQPZRLQQYSMEQ-UHFFFAOYSA-N

SMILES string

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

agency

certified by the BSC

composition

Dye content, ≥88%

Application

Certified for use in acid-fast staining procedures utilizing carbol-fuchsin; Endo medium; as Schiff′s reagent in the Periodic Acid Schiff (PAS) and Feulgen techniques; Gomori′s aldehyde fuchsin method for pancreatic B cells and hepatitis B surface antigen.

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
GHS08

signalword

Danger

hcodes

H350

Hazard Classifications

Carc. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKBC9510V
MKBM1396V
MKBK3333V
MKBC9510
MKBB3775

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H O Lyon et al.
Biotechnic & histochemistry : official publication of the Biological Stain Commission, 77(3), 121-125 (2002-09-17)
A project group working under the European Confederation of Laboratory Medicine (ECLM) presents recommendations for standardized procedures for the Feulgen-Rossenbeck-Schiff and the periodic acid-Schiff (PAS) reactions on cytological and histological material. The advantages and disadvantages of such standardized procedures are
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
J A Kiernan
Biotechnic & histochemistry : official publication of the Biological Stain Commission, 79(5-6), 203-210 (2005-03-15)
Hexazonium pararosaniline is a valuable reagent that has been used in enzyme activity histochemistry for 50 years. It is an aqueous solution containing the tris-diazonium ion derived from pararosaniline, an aminotriarylmethane dye, and it contains an excess of nitrous acid
C.I. Basic Red 9 monohydrochloride.
Report on carcinogens : carcinogen profiles, 11, III66-III67 (2004-01-01)
Ozden Tacal et al.
Journal of biochemical and molecular toxicology, 18(5), 253-256 (2004-11-19)
The formation of colorless adducts by four cationic triarylmethane dyes (TAM(+)s), methyl green (MeG(+)), malachite green (MG(+)), pararosaniline (PR(+)), and crystal violet (CV(+)) was studied spectrophotometrically at 25 degrees C, in 50 mM 3-(N-morpholino)propanesulfonic acid (MOPS) buffer (pH 8), by
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