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1,3-Benzenediol, 4-(2-benzothiazolylazo)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

3706-50-1

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3706-50-1 Usage

Type of Compound

Synthetic dye compound

Common Uses

Textile industry for dyeing fabrics
Paper industry for coloring papers

Appearance

Dark red to brownish-red

Potential Applications

Biological imaging
Medical diagnostics (due to ability to bind to certain biological molecules and tissues)

Health and Environmental Risks

May have potential health and environmental risks

Regulatory Considerations

Use and disposal should be carefully regulated and monitored

Check Digit Verification of cas no

The CAS Registry Mumber 3706-50-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,0 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3706-50:
(6*3)+(5*7)+(4*0)+(3*6)+(2*5)+(1*0)=81
81 % 10 = 1
So 3706-50-1 is a valid CAS Registry Number.

3706-50-1SDS

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-(1,3-benzothiazol-2-ylhydrazinylidene)-3-hydroxycyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 4(2-benzothiazolylazo)resorcinol

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:3706-50-1 SDS

3706-50-1Downstream Products

3706-50-1Relevant academic research and scientific papers

Azo Derivatives of Pyrocatechol, Resorcinol, and Salicylic Acid as Collectors for Sulfide Ore Flotation

Baigacheva, E. V.,Gogolishvili, V. O.,Gusev, V. Yu.

, p. 1734 - 1744 (2020/02/25)

Heterocyclic and aromatic azo derivatives of pyrocatechol, resorcinol, and salicylic acid have been investigated as collectors for the flotation of sulfide ores. The acid-base properties of the compounds were studied, their solubility in an alkaline solution was determined. It was established that the fixing of reagents on the surface of the ore occurs mainly by the chemical mechanism. Adsorption constants were calculated. It was found that most of the studied reagents exhibit collective properties with respect to sulfide copper—nickel ore. The use of mixtures of azo compounds with potassium butyl xanthogenate leads to an increase in the degree of extraction of nickel and copper, as well as the quality of the concentrates, in comparison with one butyl xanthogenate.

Polyurethanes as polymerizable dyes for hydrophobic polyester fabric

Joshi, Medha,Jauhari, Smita,Desai

, p. 2137 - 2148 (2013/02/25)

The present invention is to provide a novel benzothiazole-type polymerizable dye containing a urethane bond. A series of monomeric dyes have been prepared by diazotization of various 2-aminobenzothiiazole and coupled with Resorcinol. The polymeric dyes have been prepared by polycondensation of monomeric dyes with hexamethylene diisocyanate (HMDI), and they are characterized by molecular weight, non-aqueous conductometric titration, thermogravimetry analysis, IR, visible spectroscopy, and elemental analysis. The monomeric dyes have also been characterized by elemental analysis and IR spectra. The purity of all the dyes have been checked by thin layer chromatography, and their dyeing performance on nylon and polyester was assessed. The dyeing on polyester fiber had yellow, orange and pink shades with moderate to good light and wash fastness. Polymerizations of monomeric dyes with HMDI on dyed polyester have also been carried out. Color and dyeability of the polymeric dyes have been discussed by comparing them with their corresponding monomeric dyes. The percentage dye bath exhaustion and fixation on fiber have been found to be from good to very good. The dyeing of monomeric dyes showed very good color fastness properties, and their corresponding polymeric dyes showed excellent fastness to light, washing, perspiration, solvent resistance, and sublimation. Springer Science+Business Media B.V. 2012.

Spectrophotometric investigations of the role of the organic solvent on the acid dissociation constants of some azo dyes derived from 2-aminobenzothiazole

Ebead,Salman,Khodari,Ahmed

experimental part, p. 52 - 57 (2010/12/24)

Proton dissociation constants (pKa) of a set of hydroxyl azo dyes in various organic solvent + water mixtures have been determined. The results obtained were discussed in terms of the solvent characteristic. Effects of hydrogen-bonding interactions and solvent basicity on the ionization process have been also discussed. In a nutshell, the pKa values of the investigated compounds were found to be largely depending on both the ratio and the nature of organic cosolvent. In addition, it was very important to know with which structures we are dealing in liquid solutions and how these structures influence physicochemical properties of individual tautomers and their acidity constants. Thus, theoretical calculations have been done in order to obtain an insight into structure features and physicochemical properties of the compounds under study.

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