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Supelco

Leucomalachite Green

analytical standard

Sinonimo/i:

4,4′-Benzylidenebis(N,N-dimethylaniline)

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About This Item

Formula condensata:
C6H5CH[C6H4N(CH3)2]2
Numero CAS:
129-73-7
Peso molecolare:
330.47
Beilstein:
2140506
Numero CE:
204-961-9
Numero MDL:
MFCD00008315
Codice UNSPSC:
85151701
ID PubChem:
329761851
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Saggio

≥98.0% (HPLC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

100-102 °C (lit.)

applicazioni

cleaning products
cosmetics
food and beverages
personal care

Formato

neat

Stringa SMILE

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
WZKXBGJNNCGHIC-UHFFFAOYSA-N

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Descrizione generale

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

Applicazioni

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.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Avvertenze

Warning

Indicazioni di pericolo

H302,H341,H351,H410

Classi di pericolo

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
BCCL7375
BCCG0651
1405114V
1405114

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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)
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)
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
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