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2,5-Dithiobiurea (CAS 142-46-1)

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Alternate Names:
Hydrazodicarbothioamide
Application:
2,5-Dithiobiurea is a sulfur substituted biurea compound
CAS Number:
142-46-1
Molecular Weight:
150.23
Molecular Formula:
C2H6N4S2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2,5-Dithiobiurea is a chemical compound that functions as a crosslinking agent in polymer chemistry. It acts by forming covalent bonds between polymer chains, thereby enhancing the mechanical and thermal properties of the resulting materials. At the molecular level, 2,5-Dithiobiurea interacts with functional groups on the polymer chains, facilitating the formation of strong, durable linkages. 2,5-Dithiobiurea′s mechanism of action involves the nucleophilic addition of its sulfur atoms to electrophilic sites on the polymer, leading to the creation of a network structure. This crosslinking process contributes to the improvement of the polymer′s tensile strength, elasticity, and resistance to heat and chemicals. In experimental applications, 2,5-Dithiobiurea is utilized to modify the properties of polymers for various industrial applications.


2,5-Dithiobiurea (CAS 142-46-1) References

  1. Bioassay of 2,5-dithiobiurea for possible carcinogenicity.  |  ,. 1979. Natl Cancer Inst Carcinog Tech Rep Ser. 132: 1-107. PMID: 12799660
  2. Facile preparation of nitrogen and sulfur co-doped graphene-based aerogel for simultaneous removal of Cd2+ and organic dyes.  |  Kong, Q., et al. 2018. Environ Sci Pollut Res Int. 25: 21164-21175. PMID: 29770942
  3. In Situ S-Doping Strategy of Promoting Iron Coordinated by Nitrogen-Doped Carbon Nanosheets for Efficient Oxygen Reduction Reaction.  |  Wang, K., et al. 2022. ACS Appl Mater Interfaces. 14: 46548-46561. PMID: 36205626
  4. [5,5] Sigmatropic shift of N-phenyl-N′-(2-thiazolyl)hydrazines and N,N′-bis(2-thiazolyl)hydrazines into 2-amino-5-(p-aminophenyl)thiazoles and 5,5′-bis(2-aminothiazole) derivatives  |  Boong Won Lee, Seung Dal Lee. 2000. Tetrahedron Letters. 41: 3883-3886.
  5. Bis-thiourea Derivatives and Their Utility in Synthesis of Mono-heterocyclic, Bis-heterocyclic, and Fused Heterocyclic Systems  |  Kamal M. Dawood. 2019. Journal of Heterocyclic Chemistry. 56: 1701-1721.
  6. In situ molecular-level synthesis of N, S co-doped carbon as efficient metal-free oxygen redox electrocatalysts for rechargeable Zn–Air batteries  |  Dandan Lyu a b, Sixian Yao a, Yaser Bahari a, Syed Waqar Hasan a b, Chan Pan a, Xiaoran Zhang a, Feng Yu c, Zhi Qun Tian a, Pei Kang Shen a. 2020. 20.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2,5-Dithiobiurea, 25 g

sc-397453
25 g
$73.00