Production Method 1

58367-01-4

85-83-6

842-07-9

64-75-5

Reaction Conditions

1.1 Solvents: Ethanol ;  8 h, 180 °C

Reference

Multifunctional Carbon Dots-Based Fluorescence Detection for Sudan I, Sudan IV and Tetracycline Hydrochloride in Foods

Zhang, Min; et al, Nanomaterials, 2022, 12(23),

Sudan IV Raw materials

•  

Sudan IV Preparation Products

• Sudan I (842-07-9)
• Sudan IV (85-83-6)
• Tetracycline hydrochloride (64-75-5)

• 1. Enabling chloride salts for thermal energy storage: implications of salt purity?
  J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
• 2. Emergence of cationic polyamine dendrimersomes: design, stimuli sensitivity and potential biomedical applications
  Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026
• 3. Dissociation of large gaseous serine clusters produces abundant protonated serine octamer
  Jacob S. Jordan,Evan R. Williams Analyst, 2021,146, 2617-2625
• 4. Exciplex emission from the mixed dimer of naphthalene and 2-cyanonaphthalene in a supersonic jet
  Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
• 5. Dissociative electron attachment to HGaF4 Lewis–Br?nsted superacid
  Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Azobenzenes

Introduction to Sudan IV and Its Applications in Modern Research

Sudan IV, a compound with the chemical formula C₂₀H₁₆N₂O₂ and a CAS number of 85-83-6, is a widely recognized dye with significant applications in various scientific fields. This organic compound, known for its vibrant red color, has garnered considerable attention due to its unique chemical properties and versatile uses. In this comprehensive overview, we delve into the Sudan IV molecule, exploring its structural characteristics, industrial applications, and recent advancements in research that highlight its importance in contemporary scientific endeavors.

The molecular structure of Sudan IV consists of a naphthyl group linked to an azo dye moiety, which contributes to its strong chromophoric properties. This configuration allows Sudan IV to exhibit excellent solubility in organic solvents, making it highly effective in various laboratory settings. The compound's stability under different environmental conditions further enhances its utility in both analytical and synthetic chemistry.

In the realm of biological research, Sudan IV has found applications as a fluorescent marker and stain. Its ability to bind to lipids and cellular components makes it particularly useful in studying cellular structures and metabolic pathways. Recent studies have demonstrated its role in investigating lipid peroxidation processes, providing valuable insights into oxidative stress and cellular damage mechanisms. Researchers have leveraged the dye's affinity for lipid membranes to develop novel methodologies for assessing membrane fluidity and integrity.

The industrial significance of Sudan IV extends beyond the laboratory. It is employed as a dyeing agent in the textile industry, where its resistance to fading and environmental stability make it a preferred choice for certain applications. Additionally, its use as a pigment in paints and coatings has been explored due to its bright coloration and durability. These industrial applications underscore the compound's versatility and economic value.

Recent advancements in pharmaceutical research have also highlighted the potential of Sudan IV as a tool for drug delivery systems. Its ability to interact with biological membranes has been exploited to develop novel nanocarriers that enhance drug solubility and bioavailability. These innovations are particularly relevant in the context of targeted drug therapy, where efficient delivery mechanisms are crucial for therapeutic efficacy.

The environmental impact of Sudan IV has been another area of focus in recent years. While its persistence in aquatic ecosystems raises concerns about potential ecological risks, ongoing research aims to mitigate these issues through sustainable practices. Efforts are being made to develop environmentally friendly alternatives or modifications that reduce the compound's ecological footprint without compromising its beneficial properties.

The future prospects of Sudan IV in scientific research remain promising. Ongoing investigations into its molecular interactions and functional applications continue to uncover new possibilities across multiple disciplines. As synthetic chemistry advances, modifications to the Sudan IV structure may lead to derivatives with enhanced properties tailored for specific research needs.

In conclusion, Sudan IV (CAS no. 85-83-6) stands as a testament to the enduring relevance of traditional dyes in modern scientific exploration. Its multifaceted applications, from biological staining to industrial dyeing and pharmaceutical innovation, highlight its enduring value. As research progresses, the continued study of this compound promises to yield further insights that will shape future advancements in chemistry and related fields.

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• 1320-06-5(Oil red O)
• 2475-42-5(Phenol,4-methyl-2-[2-[3-methyl-4-[2-(3-methylphenyl)diazenyl]phenyl]diazenyl]-)
• 27969-93-3(2-Naphthalenol,1-[2-(2,6-dimethylphenyl)diazenyl]-)
• 13463-64-4(2-Naphthalenol,1-[2-[3-methyl-4-[2-(2-methylphenyl)diazenyl]phenyl]diazenyl]-)
• 6370-43-0(Solvent yellow 12)
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• 4477-79-6(oil red egn)
• 14288-70-1(2-Naphthalenol,1-[2-[4-[2-(2,5-dimethylphenyl)diazenyl]-2,5-dimethylphenyl]diazenyl]-)
• 3118-97-6(Sudan II)