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4,5,6-Triaminopyrimidine sulfate hydrate, 98+% (dry wt.), water <8%
CAS: 207742-76-5 | C4H9N5O4S | 223.21 g/mol
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Catalog number B21369.03
also known as B21369-03
Price (USD)
45.65
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Ends: 30-Jun-2026
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Each
Quantity:
1 g
Price (USD)
45.65
Special offer
Online exclusive
Ends: 30-Jun-2026
53.30Save 7.65 (14%)
Each
Specifications
Assay Percent Notes(dry wt.), water <8%
CAS207742-76-5
Chemical Name or Material4,5,6-Triaminopyrimidine sulfate hydrate
EINECS Number256-446-3
Formula Weight223.22 (Anhydrous)
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4,5,6-Triaminopyrimidine sulfate hydrate is used to prepare 2,5-anhydro-3-deoxy-N-(4',6'-diaminopyrimidin-5'yl)-D-ribo-hexonamide by reaction with 2,5-anhydro-4-O-benzyl-3-deoxy-D-ribo-hexonic acid. It is also used to prepare 4,5,6-triaminopyrimidine sulfite. Further, it acts as an intermediate in synthetic chemistry.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
4,5,6-Triaminopyrimidine sulfate hydrate is used to prepare 2,5-anhydro-3-deoxy-N-(4′,6′-diaminopyrimidin-5′yl)-D-ribo-hexonamide by reaction with 2,5-anhydro-4-O-benzyl-3-deoxy-D-ribo-hexonic acid. It is also used to prepare 4,5,6-triaminopyrimidine sulfite. Further, it acts as an intermediate in synthetic chemistry.
Solubility
Soluble in dimethyl sulfoxide.
Notes
Store in a cool place. Incompatible with strong oxidizing agents.
4,5,6-Triaminopyrimidine sulfate hydrate is used to prepare 2,5-anhydro-3-deoxy-N-(4′,6′-diaminopyrimidin-5′yl)-D-ribo-hexonamide by reaction with 2,5-anhydro-4-O-benzyl-3-deoxy-D-ribo-hexonic acid. It is also used to prepare 4,5,6-triaminopyrimidine sulfite. Further, it acts as an intermediate in synthetic chemistry.
Solubility
Soluble in dimethyl sulfoxide.
Notes
Store in a cool place. Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Leinweber, P.; Kruse, J.; Walley, F. L.; Gillespie, A.; Eckhardt, K. U.; Blyth, R.; Regier, T. Nitrogen K-edge XANES - an overview of reference compounds used to identify unknown organic nitrogen in environmental samples. J. Synchrotron Rad. 2007, 14, 500-511.
- SantaLucia, J.; Shen, L. X.; Cai, Z.; Lewis, H.; Tinoco, I. Synthesis and NMR of RNA with Selective isotopic enrichment in the bases. Nucl. Acids Res. 1995, 23 (23), 4913-4921.