Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of 1,3-adamantanediamine丨cas 10303-95-4 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.
Specifications
| Appearance | White to off-white powder |
| Purity (GC) | 99.0% min |
| HNMR | Conforms |
Transport Information
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Parameter |
Specification |
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UN Number |
3259 |
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Class |
8 |
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Packing Group |
II |
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H.S. Code |
2902199090304 |
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Stability & Reactivity |
The product is chemically stable under standard ambient conditions. |
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Storage |
Keep container tightly closed in a dry and well-ventilated area. Containers which are opened must be carefully resealed and kept upright to prevent leakage. Sealed in dry, 2-8°C |
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Condition to Avoid |
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Package |
Manufacturing Information
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Parameter |
Specification |
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Capacity |
20kg/month |
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Frequency |
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Main Export Countries |
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Capacity/Batch |
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Experience |
Production since 2019 |
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Stock |
Applications
1,3-Adamantanediamine is a rigid, bicyclic diamine widely used as an intermediate in pharmaceutical synthesis, polymer chemistry, and materials science. In medicinal chemistry, it serves as a building block for antiviral, anticancer, and CNS-active drug candidates, leveraging its sterically constrained adamantane core to enhance metabolic stability and bioactivity. In polymer and materials applications, 1,3-adamantanediamine is employed in the synthesis of polyamides, epoxy resins, and crosslinked polymers, where it imparts rigidity, thermal stability, and mechanical strength. The compound is also utilized in the development of molecular scaffolds, supramolecular assemblies, and chemical research to explore structure–activity relationships and steric effects in functional molecules.
Benefits
1,3-Adamantanediamine offers several advantages due to its unique adamantane structure, high chemical stability, and bifunctional reactivity. The diamine functionality allows selective derivatization and crosslinking reactions, while the rigid tricyclic cage provides steric bulk that can enhance solubility, stability, and target specificity in drug molecules. The compound exhibits excellent thermal and chemical stability, making it suitable for high-temperature polymerizations and demanding synthetic conditions. Its solubility in common organic solvents and reproducible reactivity ensure consistent performance in laboratory and industrial applications.
Conclusion
1,3-Adamantanediamine is a versatile diamine intermediate with broad applications in pharmaceuticals, polymers, and advanced materials. Its benefits, including rigid structure, bifunctional reactivity, and chemical stability, make it an essential building block for constructing robust, bioactive, and high-performance molecules. Continued use of 1,3-adamantanediamine supports innovation in medicinal chemistry, materials science, and synthetic research.
