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Description
1,4-Diaminoanthraquinone is a chemical compound widely used in organic reactions for the synthesis of complex molecules. It serves as a fundamental building block in chemical research, offering versatility in various synthetic pathways. This compound is derived from anthraquinone, with two amino groups attached at positions 1 and 4, enhancing its reactivity and utility. In the laboratory, it plays a crucial role in the development of dyes, pharmaceuticals, and industrial chemicals. Its structural simplicity and functional groups make it a valuable resource for chemists seeking to explore new chemical transformations.
The compound is prized for its chemical stability and controlled reactivity, which make it a preferred choice in both substitution and redox reactions. Its symmetrical structure allows for predictable chemical behavior, enabling researchers to design and execute complex synthetic routes with greater confidence. Additionally, its ability to act as an electron donor in specific reactions further broadens its applicability. These properties make it an essential reagent in organic synthesis, particularly for those working with aromatic compounds and functional group modifications.
In Indonesian laboratories, 1,4-Diaminoanthraquinone is commonly used in chemical research, especially in organic synthesis and the study of aromatic reactivity. It is a key component in the development of pigments, dyes, and pharmaceutical intermediates. Its high melting point facilitates handling during thermal processes, making it suitable for a wide range of experimental conditions. Its consistent performance and reliability make it a trusted material among researchers in the field.
Laboratory Applications
Organic synthesis applications benefit from 1,4-Diaminoanthraquinone's structural versatility and reactivity, enabling the creation of complex molecules with precise functional groups.
Pigment and dye development relies on this compound's ability to participate in redox and substitution reactions, making it ideal for synthesizing colored compounds.
Pharmaceutical research utilizes its electron-donating properties for the synthesis of drug intermediates and bioactive compounds.
Industrial chemical production benefits from its stability and controlled reactivity, supporting the creation of specialized chemical products.
Aromatic reactivity studies leverage its symmetrical structure and predictable behavior, allowing for in-depth investigation of chemical transformations.
Specifications
Brand: TCI
CAS number: 128-95-0
Category: Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes: Available in various quantities as per standard laboratory supply
Physical form: Solid
Storage note: Store in a cool, dry place away from direct sunlight and moisture
Handling and Storage
1,4-Diaminoanthraquinone should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its solid form, it is best stored in airtight containers made of glass or high-density polyethylene to avoid contamination. Laboratory personnel should handle it with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to minimize any potential exposure to fumes. Regular monitoring of storage conditions will help preserve the compound's quality and usability for research purposes.
![1,1'-Iminodianthraquinone [for Determination of Boron] (CAS 82-22-4) - TCI D0133 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510D0133.jpg?v=1767100907&width=533)
