Difurfuryldisulfide丨CAS 4437-20-1

Difurfuryldisulfide丨CAS 4437-20-1
Product Introduction:
Catalog No.: SS136398
CAS No.: 4437-20-1
Content: 96.0% min
Product Name: Difurfuryldisulfide
Certificate: Halal; Kosher
Molecular Formula: C10H10O2S2
Molecular Weight: 226.31
Synonym(s): Difurfuryl disulfide; 2,2-(Dithiodimethylene)-difuran
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Technical Parameters
Description

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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

 

Parameter

Specification

UN Number

3334

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.

Condition to Avoid

 

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.

 

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