17376
4-Hydroxy-2,5,6-triaminopyrimidine sulfate salt
technical, ≥97.0% (T)
Synonym(s):
2,5,6-Triamino-4-pyrimidol sulfate salt
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C4H7N5O · H2SO4
CAS Number:
Molecular Weight:
239.21
PubChem Substance ID:
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
4621048
MDL number:
SMILES string
OS(O)(=O)=O.Nc1nc(N)c(N)c(O)n1
InChI
1S/C4H7N5O.H2O4S/c5-1-2(6)8-4(7)9-3(1)10;1-5(2,3)4/h5H2,(H5,6,7,8,9,10);(H2,1,2,3,4)
InChI key
RSKNEEODWFLVFF-UHFFFAOYSA-N
grade
technical
assay
≥97.0% (T)
mp
≥300 °C (lit.)
Application
4-Hydroxy-2,5,6-triaminopyrimidine sulfate salt may be used in chemical synthesis.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
S W Bailey et al.
The Journal of biological chemistry, 257(14), 8253-8260 (1982-07-25)
The 5-amino substituents of two pyrimidine cofactors of rat liver phenylalanine hydroxylase, 2,5,6-triamino-4-pyrimidinone (TP) and 5-benzylamino-2,6-diamino-4-pyrimidinone (BDP), have been shown to be cleaved quantitatively by enzyme (Bailey, S. W., and Ayling, J. E. (1980) J. Biol. Chem. 255, 7774-7781). That
[Oxidation of 2,4,5-triamino-6-hydroxypyrimidine by cytochrome C and 2,6-dichlorophenolindophenol].
N Nakanisi et al.
Josai Shika Daigaku kiyo. The Bulletin of the Josai Dental University, 10(1), 15-20 (1981-01-01)
Cleavage of the 5-amino substituent of pyrimidine cofactors by phenylalanine hydroxylase.
S W Bailey et al.
The Journal of biological chemistry, 255(16), 7774-7781 (1980-08-25)
K Nakajima et al.
Acta vitaminologica et enzymologica, 7(1-2), 19-24 (1985-01-01)
It was studied with resting cells of a high flavinogenic mold, Eremothecium ashbyii, whether or not 2,4,5-triamino-6-hydroxypyrimidine (THP) is an intermediate in the early pathway of riboflavin biosynthesis. A small amounts of THP strongly inhibited riboflavin formation in the resting
A Espinosa-Mansilla et al.
Analytical biochemistry, 255(2), 263-273 (1998-02-06)
A sensitive and simple liquid chromatographic method to determine glyoxal, methylglyoxal, and diacetyl is reported. The method is based on the conversion to the corresponding pteridin derivatives (pterin, 6-methylpterin, and 6,7-dimethylpterin). The proposed method using fluorometric detection has been applied
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service