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Details

Stereochemistry ACHIRAL
Molecular Formula C20H19N3
Molecular Weight 301.385
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SOLVENT RED 41

SMILES

CC1=CC(=CC=C1N)C(C2=CC=C(N)C=C2)=C3C=CC(=N)C=C3

InChI

InChIKey=WVYMEHMNEMRCEL-SFVWPUANSA-N
InChI=1S/C20H19N3/c1-13-12-16(6-11-19(13)23)20(14-2-7-17(21)8-3-14)15-4-9-18(22)10-5-15/h2-12,21H,22-23H2,1H3/b20-14-,21-17?

HIDE SMILES / InChI
Fuchsine (rosaniline hydrochloride) is a magenta dye. Basic fuchsine is a mixture of rosaniline, pararosaniline, new fuchsine and Magenta II. Carbol fuchsin is a mixture of phenol and basic fuchsin, used in bacterial staining procedures. It is commonly used in the staining of mycobacteria as it has an affinity for the mycolic acids found in their cell membranes. The World Health Organization recommendation of 0.3% carbol fuchsin in the ZN method for staining acid-fast bacilli (AFB).

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
CASTELLANI PAINT

Approved Use

First aid antiseptic to help protect against skin infection in minor cuts, scrapes or burns
PubMed

PubMed

TitleDatePubMed
Identification of mammary carcinogens in rodent bioassays.
2002
Inhibition of human plasma cholinesterase by malachite green and related triarylmethane dyes: mechanistic implications.
2005 Aug 15
Assessment of genotoxicity of 14 chemical agents used in dental practice: ability to induce chromosome aberrations in Syrian hamster embryo cells.
2006 Feb 28
Comparative effects of cationic triarylmethane, phenoxazine and phenothiazine dyes on horse serum butyrylcholinesterase.
2008 Oct 15
Inhibition of electric eel acetylcholinesterase by triarylmethane dyes.
2008 Sep 25
Discovery of selective glucocorticoid receptor modulators by multiplexed reporter screening.
2009 Mar 24
FDA-approved drugs and other compounds tested as inhibitors of human glutathione transferase P1-1.
2013 Sep 5
Patents

Sample Use Guides

Apply a small amount of solution contatining basic fuchsin on the area one to three times daily.
Route of Administration: Topical
In Vitro Use Guide
The effect of basic fuchsin on the growth of mycoplasmas was tested at concentrations from 0.6 mg/L to 0.3 g/L.
Name Type Language
SOLVENT RED 41
Common Name English
ROSANILINE BASE
Common Name English
MAGENTA BASE [HSDB]
Common Name English
O-TOLUIDINE, 4-((P-AMINOPHENYL)(4-IMINO-2,5-CYCLOHEXADIEN-1- YLIDENE)METHYL)-
Systematic Name English
2,4-XYLIDINE, .ALPHA.(SUP 4)-(P-AMINOPHENYL)-.ALPHA.(SUP 4)-(4- IMINO-2,5-CYCLOHEXADIEN-1-YLIDENE)-
Systematic Name English
C.I. BASIC VIOLET 14, FREE BASE
Common Name English
BRILLIANT OIL CRIMSON BASE
Common Name English
BENZENAMINE, 4-((4-AMINOPHENYL)(4-IMINO-2,5-CYCLOHEXADIEN-1-YLIDENE)METHYL)-2-METHYL-
Systematic Name English
CI 42510B
Common Name English
4-((4-AMINOPHENYL)(4-IMINOCYCLOHEXA-2,5-DIEN-1- YLIDENE)METHYL)-O-TOLUIDINE
Systematic Name English
C.I. SOLVENT RED 41
Common Name English
Code System Code Type Description
CHEBI
87666
Created by admin on Fri Dec 15 18:48:14 GMT 2023 , Edited by admin on Fri Dec 15 18:48:14 GMT 2023
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CAS
3248-93-9
Created by admin on Fri Dec 15 18:48:14 GMT 2023 , Edited by admin on Fri Dec 15 18:48:14 GMT 2023
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ECHA (EC/EINECS)
221-832-2
Created by admin on Fri Dec 15 18:48:14 GMT 2023 , Edited by admin on Fri Dec 15 18:48:14 GMT 2023
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EPA CompTox
DTXSID0043844
Created by admin on Fri Dec 15 18:48:14 GMT 2023 , Edited by admin on Fri Dec 15 18:48:14 GMT 2023
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FDA UNII
I8F3948441
Created by admin on Fri Dec 15 18:48:14 GMT 2023 , Edited by admin on Fri Dec 15 18:48:14 GMT 2023
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HSDB
2955
Created by admin on Fri Dec 15 18:48:14 GMT 2023 , Edited by admin on Fri Dec 15 18:48:14 GMT 2023
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