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4-METHOXY-2-PHENYLAZO-1-NAPHTHOL is a chemical compound that belongs to the azo dyes class. It is characterized by its dark red to brown powder form, which is insoluble in water but soluble in organic solvents. 4-METHOXY-2-PHENYLAZO-1-NAPHTHOL is recognized for its capacity to form brightly colored complexes with metal ions, a property that is particularly valuable in various applications.

59900-33-3

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59900-33-3 Usage

Uses

Used in Textile Industry:
4-METHOXY-2-PHENYLAZO-1-NAPHTHOL is used as a colorant for imparting vibrant hues to textiles. Its solubility in organic solvents facilitates its application in dyeing processes, enhancing the colorfastness and aesthetic appeal of fabrics.
Used in Food Industry:
In the food industry, 4-METHOXY-2-PHENYLAZO-1-NAPHTHOL serves as a colorant to add visual appeal to food products. Its ability to create bright and attractive colors makes it a valuable ingredient in the formulation of food dyes.
Used in Analytical Chemistry:
4-METHOXY-2-PHENYLAZO-1-NAPHTHOL is utilized as a reagent in analytical chemistry for the detection and determination of heavy metals. Its property of forming colored complexes with metal ions aids in the qualitative and quantitative analysis of metal content in various samples.
Used in Antioxidant Applications in the Food Industry:
4-METHOXY-2-PHENYLAZO-1-NAPHTHOL has been studied for its potential as a natural antioxidant. It is being explored for its ability to prevent or slow down the oxidation of food products, thereby extending their shelf life and maintaining their quality.
Used in Antimicrobial Applications:
4-METHOXY-2-PHENYLAZO-1-NAPHTHOL is also being investigated for its antimicrobial properties, which could be harnessed to inhibit the growth of microorganisms in various settings, including food preservation and medical applications.
Used in Anticancer Research:
4-METHOXY-2-PHENYLAZO-1-NAPHTHOL is under research for its potential anticancer properties. Its possible role in combating cancer cells is being explored, with the aim of developing new therapeutic agents.
While 4-METHOXY-2-PHENYLAZO-1-NAPHTHOL shows promise in these areas, further research is essential to fully understand its potential uses and to ensure the safety and efficacy of its applications.

Check Digit Verification of cas no

The CAS Registry Mumber 59900-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,0 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59900-33:
(7*5)+(6*9)+(5*9)+(4*0)+(3*0)+(2*3)+(1*3)=143
143 % 10 = 3
So 59900-33-3 is a valid CAS Registry Number.

59900-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methoxy-2-phenylazo-1-naphthol

1.2 Other means of identification

Product number -
Other names 4-methoxy-2-(phenylhydrazinylidene)naphthalen-1-one

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:59900-33-3 SDS

59900-33-3Downstream Products

59900-33-3Relevant academic research and scientific papers

15N, 13C and 1H NMR study of tautomerism in 2-(phenyldiazenyl-4-substituted naphthalen-1-ols. Influence of substitution in passive components on azo-hydrazo tautomerism

Neuerová, Zdeňka,Ly?ka, Antonín

, (2021/02/03)

The one- and two-dimensional 15N, 13C and 1H NMR spectra of benzenediazonium chloride coupling product with 4-R-naphthalene-1-ols (R = NO2 (1), Br (2), Cl (3), H (4), OCH3 (5)) were measured and analysed. It was found that the reaction products exist predominantly in hydrazone forms. Contrary to previously published influence of substituents in diazonium salts, where more electron acceptor types of substituents cause increase contents of hydrazo forms, the situation in compounds 1–5 is completely opposite. Moreover, hydrazone content in 4-nitro-2-[(E)-(4-nitro-phenyl)diazenyl]naphtalen-1-ol (6) combining substitution both in position 4 of passive component and position 4 of active component (i. e. diazonium salt) is higher compared with that in 4-nitro-2-[(E)-(phenyl)diazenyl]naphtalen-1-ol (1).

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