Welcome to LookChem.com Sign In|Join Free

CAS

  • or

129-73-7

Post Buying Request

129-73-7 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

129-73-7 Usage

Description

Leucomalachite Green is a metabolite of Malachite Green, which is a colorless compound with various applications across different industries. It exhibits chemical properties such as being white to light brown, light green, or light blue in appearance.

Uses

Used in Textile Industry:
Leucomalachite Green is used as a dye for directly coloring silk, wool, jute, and leather. It is also used for dyeing cotton after mordanting, providing a vibrant and lasting color to the fabric.
Used in Biological Research:
As a biological stain, Leucomalachite Green is employed in the study of various biological samples, aiding in the visualization and analysis of cellular structures and components.
Used in Clinical Research:
Leucomalachite Green serves as a clinical reagent, specifically for the inorganic phosphate assay, which is crucial in understanding various physiological processes and diagnosing certain medical conditions.
Used in Chemical Analysis:
The compound is used as a spot test reagent for detecting sulfurous acid and cerium, which are essential in identifying specific chemical compounds and their concentrations in various samples.
Used as an Acid-Base Indicator:
Leucomalachite Green functions as an acid-base indicator, with a color change at different pH levels. It turns yellow at pH 0.0, green at pH 2.0, and colorless at pH 14, making it a useful tool in determining the acidity or alkalinity of a solution.
Used in Medical Diagnostics:
Leucomalachite Green is a reagent for the quantitative colorimetric micro determination of hemoglobin and other heme compounds, which is vital in diagnosing and monitoring various blood-related disorders and conditions.

Purification Methods

Crystallise it from 95% EtOH (10mL/g), then from *benzene/EtOH, and finally from pet ether. [Beilstein 13 H 275, 13 II 89, 13 II 135, 13 III 529, 13 481.]

Check Digit Verification of cas no

The CAS Registry Mumber 129-73-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 129-73:
(5*1)+(4*2)+(3*9)+(2*7)+(1*3)=57
57 % 10 = 7
So 129-73-7 is a valid CAS Registry Number.

129-73-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (43758)  Leucomalachite Green   

  • 129-73-7

  • 2g

  • 137.0CNY

  • Detail
  • Alfa Aesar

  • (43758)  Leucomalachite Green   

  • 129-73-7

  • 10g

  • 655.0CNY

  • Detail
  • Sigma-Aldrich

  • (78567)  LeucomalachiteGreen  certified reference material, TraceCERT®

  • 129-73-7

  • 78567-25MG

  • 1,547.91CNY

  • Detail
  • Sigma-Aldrich

  • (78567)  LeucomalachiteGreen  certified reference material, TraceCERT®

  • 129-73-7

  • 78567-100MG

  • 2,337.66CNY

  • Detail
  • Sigma-Aldrich

  • (69669)  LeucomalachiteGreen  analytical standard

  • 129-73-7

  • 69669-25MG

  • 360.36CNY

  • Detail

129-73-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name LEUCOMALACHITE GREEN

1.2 Other means of identification

Product number -
Other names 4-[[4-(dimethylamino)phenyl]-phenylmethyl]-N,N-dimethylaniline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:129-73-7 SDS

129-73-7Related news

Simultaneous determination of malachite green and its metabolite LEUCOMALACHITE GREEN (cas 129-73-7) in eel plasma using post-column oxidation09/27/2019

A rapid HPLC method with solid-phase extraction (SPE) clean-up for malachite green (MG) and leucomalachite green (LMG) in eel plasma was developed. MG and LMG were extracted with a buffered methanolic solution. The extract was subjected to aromatic sulphonic acid SPE. MG and LMG were eluted fr...detailed

129-73-7Relevant articles and documents

Solvent-free synthesis of 4,4-diaminotriarylmethanes-leuco malachite materials in the presence of FePO4

Behbahani, Farahnaz K.,Khademloo, Elham

, p. 1507 - 1510 (2014)

A fast, efficient and versatile route for the synthesis of 4,4-diaminotriarylmethanes is reported using N,N-dimethyl aniline and aryl aldehydes in presence of FePO4 under solvent-free condition at 100°C.

The novel two step synthesis of CuO/ZnO and CuO/CdO nanocatalysts for enhancement of catalytic activity

Kumaraguru, K.,Sankaran, A.

, (2020)

In the present investigation, Copper oxide (CuO)/Zinc oxide (ZnO) and CuO/cadmium oxide (CdO) nanocomposites (NCs) were fabricated by a simple two-step process involving co-precipitation technique and hydrothermal approach for the first time. The Powder X-ray Diffraction (PXRD) pattern demonstrates the existence of monoclinic, hexagonal and cubic phase structure of CuO/ZnO and CuO/CdO NCs. The absorption spectrum of the material was obtained via UV–Visible Spectroscopy and the band-gap value is calculated using Tauc's relation as 1.7 eV, 2.8 eV and 2.75 eV respectively for pure, CuO/ZnO and CuO/CdO NCs. The FESEM images gave the spherical and stone-like morphologies in the prepared CuO/ZnO and CuO/CdO NCs. At room temperature, CuO/ZnO and CuO/CdO NCs act as superior catalyst for the reduction of Rhodamine B (RhB) and Malachite Green (MG) dyes and degradation efficiency attained to be 77.26%, 73.15% for RhB and 79.82%, 74.69 for MG, respectively.

Silver-catalyzed tandem 5- And 6-endo-cyclizationsviaconcomitant yne-ol-imine activation: selective entry to 2-aryldihydrofuroquinolines

Das, Prasanta,Karmakar, Swastik,Kundu, Sandip

, p. 16112 - 16118 (2021/09/22)

A silver(i) catalyzed domino imination-intramolecular biheterocyclization-aromatization cascade has been developed to construct 2-aryl/-heteroaryl dihydrofuroquinolines in moderate to good yield using an aldehyde and unprotected 4-(2-aminophenyl)but-3-yn-1-ol as precursors. Sequential Ag-(i)-induced 5-endo-digcyclization of the yne-ol part and 6-endo-trigcyclization of a proposed Ag-bound imine, followed by aromatization, furnish the furoquinoline derivatives.

COMPOSITIONS, METHODS, AND TEST KITS FOR DETERMINING AUTHENTICITY

-

Paragraph 0143-0144, (2019/04/30)

The present disclosure provides composition having at least one leuco composition conforming to Formula (I): [in-line-formulae]Ar1Ar2Ar3CH??(I)[/in-line-formulae] wherein Ar2 and Ar3 are independently a carbocyclic aryl or heteroaryl, and Ar1 is selected from the group consisting of: unsubstituted phenyl, electron deficient carbocyclic aryl, and heteroaryl. The present disclosure also provides a method of detecting an authentic composition and test kits for detecting authentic compositions.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 129-73-7