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Specifications
| Grade | Food grade |
| Appearance | Yellow to brown oily liquid |
| Content | 96.0% min |
| Odor | Have an air of sulfur, diluted with strong baked, barbecue, nut |
| RI (refractive index) (20℃) | 1.585~1.598 |
| Relative density (25℃/25℃) | 1.229~1.248 |
Transport Information
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Parameter |
Specification |
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UN Number |
3334 |
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Class |
9 |
|
Packing Group |
III |
|
H.S. Code |
2932190090303 |
|
Stability & Reactivity |
The product is chemically stable under standard ambient conditions. |
|
Storage |
Keep container tightly closed in a dry and well-ventilated place. |
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Condition to Avoid |
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Package |
Applications
Difurfuryldisulfide is primarily used as a sulfur-containing organic compound in chemical synthesis and research. It serves as a precursor for the preparation of disulfide-linked molecules, polymers, and heterocyclic derivatives. The compound finds application in materials chemistry, where it can be incorporated into polymers or resins to introduce sulfur-based crosslinking and redox-responsive properties. It is also used in pharmaceutical and agrochemical research as an intermediate for synthesizing biologically active compounds, where the disulfide bond can play a role in redox regulation or controlled release of active species. Additionally, Difurfuryldisulfide is employed in studies of sulfur-containing heterocycles and organosulfur reaction mechanisms.
Benefits
The benefits of Difurfuryldisulfide include its chemical stability, defined disulfide functionality, and versatility in synthetic transformations. The disulfide linkage allows for selective cleavage or formation under mild oxidative or reductive conditions, making it useful for redox-sensitive applications. Its furan rings provide additional sites for chemical modification, enabling the synthesis of functionalized molecules and polymers. The compound is compatible with various solvents and reaction conditions, ensuring reproducible performance in laboratory and industrial syntheses. Its dual functionality as both a reactive disulfide and furan-containing compound enhances its utility in advanced chemical research.
Conclusion
Difurfuryldisulfide is a versatile sulfur-containing intermediate used in organic synthesis, polymer chemistry, and pharmaceutical research. Its disulfide bond, combined with furan functionality, provides opportunities for redox-sensitive reactions, crosslinking, and functionalization. These properties make it a valuable compound for the development of advanced materials, bioactive molecules, and specialized chemical intermediates.

