2481-94-9 Usage
Uses
Used in Oil, Wax, and Fat Coloring:
Solvent Yellow 56 is used as a coloring agent for oil, wax, and fat class materials due to its ability to provide a vibrant and stable color.
Used in Plastic Coloring:
Solvent Yellow 56 is used as a coloring agent in the plastic industry to impart a consistent and long-lasting color to plastic products.
Used in Printing Ink Coloring:
Solvent Yellow 56 is used as a coloring agent in the production of printing inks, ensuring a strong and durable color in printed materials.
Used in Paint Coloring:
Solvent Yellow 56 is used as a coloring agent in the paint industry to provide a stable and vibrant color for various paint applications.
Used in Smoke Dye:
Solvent Yellow 56 can also be used as a coloring agent for smoke dye, offering a stable and long-lasting color in various smoke-related applications.
Chemical Properties:
Solvent Yellow 56 is a light brown powder that is insoluble in water, sodium carbonate (5%), and hydrochloric acid (5%). It has a stable melting point and is classified under the ISO standard.
Preparation
aniline diazotization, and N,N-diethylbenzenamine coupling.
Flammability and Explosibility
Notclassified
Safety Profile
Mutation data reported. Whenheated to decomposition it emits toxic fumes of NOx.
Standard
Light Fastness
Melting point
Stable
Check Digit Verification of cas no
The CAS Registry Mumber 2481-94-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,8 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2481-94:
(6*2)+(5*4)+(4*8)+(3*1)+(2*9)+(1*4)=89
89 % 10 = 9
So 2481-94-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H19N3/c1-3-19(4-2)16-12-10-15(11-13-16)18-17-14-8-6-5-7-9-14/h5-13H,3-4H2,1-2H3
2481-94-9Relevant academic research and scientific papers
A CONTINUOUS PROCESS FOR THE SYNTHESIS OF AZO DYES INVOLVING IN-SITU GENERATION OF DIAZONIUM SALTS
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Paragraph 0053-0054, (2021/05/21)
The present disclosure provides a continuous process for the synthesis coupled compounds of diazonium salts including azo dyes involving in-situ generation of diazonium salts. It further discloses a set up to carry out the process for the synthesis of coupled compounds of diazonium salts.
Photochemical Decomposition of 4-Arylazo- and 4-Arylazoxy-N,N-dialkylaniline N-Oxides
Albini, Angelo,Fasani, Elisa,Moroni, Micaela,Pietra, Silvio
, p. 1439 - 1444 (2007/10/02)
The 4-aryl-N,N-dialkylaniline N-oxides (1a-c) decompose on u.v. irradiation in aprotic solvents, undergoing deoxygenation as well as intramolecular hydrogen abstraction, to give amides and dealkylated products.The latter process is more important for the diethyl derivative (1b) (photoCope elimination).Visible irradiation is ineffective.The 4-arylazoxy-N,N-dialkylaniline N-oxides (2a-d) undergo photochemical deoxygenation from the amino group (major process) as well as from the azo group.The mechanism of these photoprocesses is discussed in general and in relation to the possible involvement of these N-oxide derivatives in photofading of the related azo dyes.
