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Catalog Number:
17099
CAS Number:
116-82-5
1-Amino-2-bromo-4-hydroxy anthraquinone
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Product Information

1-Amino-2-bromo-4-hydroxy anthraquinone is a versatile chemical compound widely utilized in various industrial applications, particularly in the dye and pigment sectors. This compound is known for its vibrant color properties, making it an excellent choice for producing high-performance dyes used in textiles, paper, and plastics. Its unique structure allows for effective binding to substrates, ensuring durability and resistance to fading, which is crucial for products exposed to light and environmental conditions.

In addition to its applications in dye manufacturing, 1-Amino-2-bromo-4-hydroxy anthraquinone is also explored in the field of organic electronics, where it serves as a potential component in organic semiconductors and photovoltaic devices. Researchers appreciate its stability and efficiency in charge transport, which can enhance the performance of electronic devices. With its multifunctional properties, this compound stands out as a valuable asset for professionals seeking innovative solutions in both the chemical and electronic industries.

CAS Number
116-82-5
Molecular Formula
C14H8BrNO3
Molecular Weight
318.13
MDL Number
MFCD00019156
PubChem ID
8320
Conditions
Store at 0-8°C
General Information
CAS Number
116-82-5
Molecular Formula
C14H8BrNO3
Molecular Weight
318.13
MDL Number
MFCD00019156
PubChem ID
8320
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1-Amino-2-bromo-4-hydroxy anthraquinone is widely utilized in research focused on:

  • Dyes and Pigments: This compound is used in the production of vibrant dyes for textiles and paper, offering excellent color fastness and stability, making it ideal for industries requiring long-lasting colors.
  • Pharmaceuticals: It serves as a precursor in synthesizing various pharmaceutical compounds, particularly in developing anti-cancer agents, due to its unique chemical structure that can interact with biological systems.
  • Analytical Chemistry: The compound is employed as a reagent in analytical methods, such as spectrophotometry, to detect and quantify specific substances in complex mixtures, enhancing the accuracy of research results.
  • Biological Research: It is used in studies investigating the effects of anthraquinone derivatives on cellular processes, providing insights into potential therapeutic applications and mechanisms of action.
  • Environmental Applications: The compound is explored for its potential in wastewater treatment processes, where it can help in the degradation of pollutants, contributing to cleaner water systems.

Citations