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Specifications
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Appearance |
Gray-white powder |
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Purity (HPLC) |
98.5% min |
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Purity (chemical method) |
98% min |
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Melting point |
256–258℃ |
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Alkali insoluble substance |
0.1% max |
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Salt content |
0.1% max |
Transport Information
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Parameter |
Specification |
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UN Number |
3077 |
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Class |
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Packing Group |
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H.S. Code |
2907299090 |
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Stability & Reactivity |
The product is chemically stable under standard ambient conditions. |
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Storage |
Tightly closed. Store in a closed, dry, ventilated place |
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Condition to Avoid |
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Package |
Chemical Overview
1,5-Dihydroxy naphthalene丨CAS 83-56-7 is a dihydroxy-substituted aromatic hydrocarbon that belongs to the naphthol family. Its symmetric structure makes it a versatile intermediate in organic chemistry and industrial processes.
Applications of 1,5-Dihydroxynaphthalene
1. Dye and Pigment Industry
Used as a key intermediate in azo dye synthesis, where it reacts with diazonium salts to form stable, vividly colored compounds.
Applied in the production of acid dyes, reactive dyes, and pigments for textiles, leather, and plastics.
Its electron-rich hydroxyl groups enhance color intensity and stability in dyes.
2. Pharmaceutical and Fine Chemical Synthesis
Serves as a starting material in the synthesis of biologically active compounds and pharmaceuticals.
Can be incorporated into anti-inflammatory, antimicrobial, and anticancer agents, particularly in research contexts.
Used in synthetic pathways for naphthoquinones and related bioactive heterocycles.
3. Polymer and Resin Chemistry
1,5-Dihydroxy naphthalene丨CAS 83-56-7 functions as a monomer or modifier in the synthesis of specialty polymers and resins with aromatic content.
Enhances thermal and UV resistance in high-performance plastics and coatings.
4. Analytical and Photochemical Applications
Acts as a reagent or chromophore in analytical chemistry and UV-visible spectroscopy.
Employed in photochemical studies and materials for photovoltaic or light-sensitive applications.
5. Chemical Research and Development
A valuable compound in academic and industrial R&D, especially for developing new organic reactions and functionalized aromatic compounds.
Used as a model compound for studying aromatic substitution, hydrogen bonding, and electronic effects.
Benefits of 1,5-Dihydroxynaphthalene
1. Versatile Reactivity
The presence of two hydroxyl groups on an aromatic ring provides multiple sites for functionalization, including etherification, esterification, oxidation, and sulfonation.
Useful in designing molecules with tunable electronic and physical properties.
2. High Chemical Stability
Stable under normal storage and handling conditions.
Can withstand elevated temperatures and exposure to light when incorporated into products.
3. Enhances Color and Performance in Dyes
Provides deep color hues and high lightfastness when used in dye formulations.
Improves solubility and binding of dyes to various substrates such as cotton, wool, and nylon.
4. Facilitates High-Value Compound Synthesis
Enables synthesis of complex aromatic and heterocyclic systems, which are otherwise difficult to access.
Offers a cost-effective route to many industrial and research chemicals.
5. Available and Scalable
Commercially available with high purity.
Production methods are well-established, making it suitable for large-scale industrial applications as well as laboratory-scale research.
Conclusion
1,5-Dihydroxy naphthalene丨CAS 83-56-7 is a multifunctional aromatic compound primarily used in the dye, pharmaceutical, polymer, and chemical research industries. Its two hydroxyl groups make it highly reactive and versatile for organic synthesis, while its stable structure lends itself to applications in high-performance materials and colorants. The compound's value in producing vivid, long-lasting dyes and its potential in drug development and advanced materials underscore its importance across both traditional manufacturing and modern scientific innovation.

