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Details

Stereochemistry ACHIRAL
Molecular Formula C26H33N3.2Cl
Molecular Weight 458.466
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHYL GREEN

SMILES

[Cl-].[Cl-].CN(C)C1=CC=C(C=C1)C(C2=CC=C(C=C2)[N+](C)(C)C)=C3C=CC(C=C3)=[N+](C)C

InChI

InChIKey=DWCZIOOZPIDHAB-UHFFFAOYSA-L
InChI=1S/C26H33N3.2ClH/c1-27(2)23-14-8-20(9-15-23)26(21-10-16-24(17-11-21)28(3)4)22-12-18-25(19-13-22)29(5,6)7;;/h8-19H,1-7H3;2*1H/q+2;;/p-2

HIDE SMILES / InChI

Description
Sources: DOI: 10.1201/9780849382192.ch11, Sabnis R.W., 'Handbook of Acid-Base Indicators' (2007), p. 149

A DNA stain used as a tracking dye in acid buffers for electrophoresis. Methyl Green was used as a topical antiseptic, however, it was withdrawn due to unwanted effects. The traditional Methyl Green has not manufactured for decades. The dye sold as Methyl Green is more accurately described as Ethyl Green. Both, Methyl Green and Ethyl Green are sold as double zinc salts.

Approval Year

PubMed

PubMed

TitleDatePubMed
The Nature of the Specificity of Methyl Green for Chromatin.
1949 Feb
Spectrophotometry of dyes. I. Methyl green. II. Pyronin.
1953 Nov
On the nature of the deoxyribonucleic acid-methyl green reaction.
1958 Sep 25
Patents

Sample Use Guides

Methyl green inhibited B.aerogenis, B.coli, B.typhosus, with the inhibiting dilution of 1200 and B.proteus with he inhibiting dilution of 2700.
Name Type Language
METHYL GREEN
Common Name English
BASIC BLUE 20
Common Name English
DOUBLE GREEN
Common Name English
AMMONIUM, (.ALPHA.-(P-(DIMETHYLAMINO)PHENYL)-.ALPHA.-(4- (DIMETHYLIMINIO)-2,5-CYCLOHEXADIEN-1-YLIDENE)-P- TOLYL)TRIMETHYL-, DICHLORIDE
Systematic Name English
C.I. BASIC VIOLET 3, COMPD. WITH CHLOROMETHANE (1:1)
Common Name English
BENZENAMINIUM, 4-((4-(DIMETHYLAMINO)PHENYL)(4- (DIMETHYLIMINIO)-2,5-CYCLOHEXADIEN-1-YLIDENE)METHYL)-N,N,N- TRIMETHYL-, CHLORIDE (1:2)
Systematic Name English
C.I. BASIC BLUE 20
Common Name English
4-((4-(DIMETHYLAMINO)PHENYL)(4-(DIMETHYLIMINIO)CYCLOHEXA- 2,5-DIEN-1-YLIDENE)METHYL)-N,N,N-TRIMETHYLANILINIUM DICHLORIDE
Systematic Name English
BENZENAMINIUM, 4-((4-(DIMETHYLAMINO)PHENYL)(4- (DIMETHYLIMINIO)-2,5-CYCLOHEXADIEN-1-YLIDENE)METHYL)-N,N,N- TRIMETHYL-, DICHLORIDE
Systematic Name English
Code System Code Type Description
FDA UNII
6P7U4T9BXA
Created by admin on Sat Dec 16 09:39:50 GMT 2023 , Edited by admin on Sat Dec 16 09:39:50 GMT 2023
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WIKIPEDIA
Methyl green
Created by admin on Sat Dec 16 09:39:50 GMT 2023 , Edited by admin on Sat Dec 16 09:39:50 GMT 2023
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PUBCHEM
6727
Created by admin on Sat Dec 16 09:39:50 GMT 2023 , Edited by admin on Sat Dec 16 09:39:50 GMT 2023
PRIMARY
CHEBI
87649
Created by admin on Sat Dec 16 09:39:50 GMT 2023 , Edited by admin on Sat Dec 16 09:39:50 GMT 2023
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CAS
82-94-0
Created by admin on Sat Dec 16 09:39:50 GMT 2023 , Edited by admin on Sat Dec 16 09:39:50 GMT 2023
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CAS
54327-10-5
Created by admin on Sat Dec 16 09:39:50 GMT 2023 , Edited by admin on Sat Dec 16 09:39:50 GMT 2023
NO STRUCTURE GIVEN
ECHA (EC/EINECS)
201-447-6
Created by admin on Sat Dec 16 09:39:50 GMT 2023 , Edited by admin on Sat Dec 16 09:39:50 GMT 2023
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EPA CompTox
DTXSID60889419
Created by admin on Sat Dec 16 09:39:50 GMT 2023 , Edited by admin on Sat Dec 16 09:39:50 GMT 2023
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