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Merck

69669

Supelco

Leucomalachitgrün

analytical standard

Synonym(e):

4,4′-Benzyliden-bis-(N,N-dimethylanilin)

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About This Item

Lineare Formel:
C6H5CH[C6H4N(CH3)2]2
CAS-Nummer:
Molekulargewicht:
330.47
Beilstein:
2140506
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
85151701
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Assay

≥98.0% (HPLC)

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

mp (Schmelzpunkt)

100-102 °C (lit.)

Anwendung(en)

cleaning products
cosmetics
food and beverages
personal care

Format

neat

SMILES String

CN(C)c1ccc(cc1)C(c2ccccc2)c3ccc(cc3)N(C)C

InChI

1S/C23H26N2/c1-24(2)21-14-10-19(11-15-21)23(18-8-6-5-7-9-18)20-12-16-22(17-13-20)25(3)4/h5-17,23H,1-4H3

InChIKey

WZKXBGJNNCGHIC-UHFFFAOYSA-N

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Allgemeine Beschreibung

Leucomalachite green is a triphenylmethane dye and a metabolite of malachite green.

Anwendung

Leucomalachite green may be used as an analytical reference standard for the quantification of the analyte in fish samples using different chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Verpackung

Bottomless glass bottle. Contents are inside inserted fused cone.

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Muta. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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Kunden haben sich ebenfalls angesehen

Determination of malachite green and leucomalachite green in edible goldfish muscle by liquid chromatography?ion trap mass spectrometry
Lee C-K, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 843(2), 247-251 (2006)
Hongping Wan et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 49(12), 3031-3037 (2011-10-19)
Malachite green (MG) had been extensively used worldwide in the past few decades as an effective fungicide, bactericide, ectoparasiticide, and antiprotozoan on fish. It is rapidly and extensively metabolized to leucomalachite green (LMG) in fishes. To study the developmental toxicity
Kevin J Farrugia et al.
Science & justice : journal of the Forensic Science Society, 51(3), 110-121 (2011-09-06)
This study investigates the optimisation of peroxidase based enhancement techniques for footwear impressions made in blood on various fabric surfaces. Four different haem reagents: leuco crystal violet (LCV), leuco malachite green (LMG), fluorescein and luminol were used to enhance the
Jun Bae Lee et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 27(7), 953-961 (2010-06-15)
This paper presents analysis of malachite green (MG) and crystal violet (CV) residues in processed fish products. Samples were homogenized and extracted with ammonium acetate buffer and acetonitrile. The extracted residues were partitioned into dichloromethane, in situ oxidized to chromic
A simple and rapid method for the identification and quantification of malachite green and its metabolite in hake by HPLC?MS/MS
Nebot C, et al.
Food Control, 31(1), 102-107 (2013)

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