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2051-85-6

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2051-85-6 Usage

Chemical Properties

red-orange powder

Uses

Sudan Orange G is an oil soluble synthetic dye. Sudan Orange G can be degraded by a bacterial strain known as Pseudomonas putida MET94. Dyes and metabolites, Environmental Testing

Preparation

aniline diazo, Coupled with resorcinol.

Properties and Applications

bright orange. Yellow orange powder, melting point: 150 ~ 170 ℃ (usually products do not pure). Soluble in ethanol and aether (yellow), in the ethanol solubility of 0.2 ~ 0.3 g / 100ml, slightly soluble in water, but soluble in vegetable oil. The strong sulfuric acid to red light brown, for yellow brown solution diluted, and then into a dark orange precipitation; In 2% of sodium hydroxide solution (heating) for orange brown solution. Its water solution and strong hydrochloric acid color the darker, and then generate a shallow brown precipitation. Sun of resistance, alkali resistance is bad. And C.I.Solvent Orange 1?the same chemical structure.

Purification Methods

Crystallise the dye from hot EtOH (charcoal). [Beilstein 16 IV 264.]

Check Digit Verification of cas no

The CAS Registry Mumber 2051-85-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2051-85:
(6*2)+(5*0)+(4*5)+(3*1)+(2*8)+(1*5)=56
56 % 10 = 6
So 2051-85-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N2O2/c15-10-6-7-11(12(16)8-10)14-13-9-4-2-1-3-5-9/h1-8,15-16H/b14-13+

2051-85-6 Well-known Company Product Price

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  • Sigma-Aldrich

  • (43207)  SudanOrangeG  analytical standard

  • 2051-85-6

  • 43207-25MG

  • 360.36CNY

  • Detail

2051-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Sudan Orange G

1.2 Other means of identification

Product number -
Other names sudan orange-G

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:2051-85-6 SDS

2051-85-6Relevant articles and documents

Blue-light-induced processes in a series of azobenzene poly(ester imide)s

Kozanecka-Szmigiel, Anna,Konieczkowska, Jolanta,Szmigiel, Dariusz,Antonowicz, Jerzy,Ma?ecki, Jan,Schab-Balcerzak, Ewa

, p. 177 - 185 (2017)

We report on a series of photoresponsive azobenzene poly(ester imide)s thermally converted from their precursor poly(ester amic acid)s. Thermal properties as well as ability for efficient photoinduced chromophore orientation and polymer mass transport under linearly polarized blue irradiation were investigated, focusing on the effect of azo chromophore location within polymer chain. The amount of chromophore alignment studied in the experiment on photoinduced birefringence differed by a factor of l.5 between the materials. Despite the fact that the generated birefringence was of the same order of magnitude, very large differences in efficiency of surface relief grating formation were seen. Specific features of photoresponsive behaviour of the polymers were shown to correlate with the presence or the absence of intrachain C[sbnd]H?π interaction between azobenzene hydrogen and aromatic imide structure, which was revealed by density functional theory (DFT) calculations. Advantageous chromophore location next to the imide groups for effective light-driven processes was shown.

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.

A Photobasic Functional Group

He, Jie,Kimani, Flora W.,Jewett, John C.

supporting information, p. 9764 - 9767 (2015/08/24)

Controlling chemical reactivity using light is a longstanding practice within organic chemistry, yet little has been done to modulate the basicity of compounds. Reported herein is a triazabutadiene that is rendered basic upon photoisomerization. The pH of an aqueous solution containing the water-soluble triazabutadiene can be adjusted with 350 nm light. Upon synthesizing a triazabutadiene that is soluble in aprotic organic solvents, we noted a similar light-induced change in basicity. As a proof of concept we took this photobase and used it to catalyze a condensation reaction.

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