| Weight | 330.475 g/mol |
|---|---|
| Formula | C23H26N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 5 |
Leucomalachite green (129-73-7)
4,4'-benzylidenebis(N,N-dimethylaniline)
Score:
#778 in Physics
,
#1867 in Biology
,
#2245 in Chemistry
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- Toxicity and metabolism of malachite green and leucomalachite green during short-term feeding to Fischer 344 rats and B6C3F1 mice (Chemico-Biological Interactions, 1999)
- Determination of malachite green and leucomalachite green in carp muscle by liquid chromatography with visible and fluorescence detection (Journal of Chromatography A, 2005)
- Synthesis and Characterization of N-Demethylated Metabolites of Malachite Green and Leucomalachite Green (Chemical Research in Toxicology, 2003)
- Effects of malachite green (MG) and its major metabolite, leucomalachite green (LMG), in two human cell lines. (Toxicology in Vitro, 2005)
- Quantitative and Confirmatory Analyses of Malachite Green and Leucomalachite Green Residues in Fish and Shrimp (Journal of Agricultural and Food Chemistry, 2006)
- Confirmatory analysis of malachite green, Leucomalachite green, crystal violet and leucocrystal violet in salmon by liquid chromatography-tandem mass spectrometry (Analytica Chimica Acta, 2007)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H341: Suspected of causing genetic defects
Warning Germ cell mutagenicity - Category 2 - 4,4'-benzylidenebis(N,N-dimethylaniline)
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SMILESCN(C)C1=CC=C(C=C1)C(C2=CC=CC=C2)C3=CC=C(C=C3)N(C)C
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InChIKeyWZKXBGJNNCGHIC-UHFFFAOYSA-N
- Pubchem - Leucomalachite green
- Wikipedia - leucomalachite green
Malachite green is an organic compound that is used as a dyestuff and controversially as an antimicrobial in aquaculture. Malachite green is traditionally used as a dye for materials such as silk, leather, and paper. Despite its name the dye is not prepared from the mineral malachite, and the name just comes from the similarity of color.
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Synthesis
N,N-dimethylaniline
+
Reactant
(Friedel-Crafts alkylation)
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