17376
2,4,5-三氨基-6-羟基嘧啶 硫酸盐
technical, ≥97.0% (T)
别名:
2,5,6-三氨基-4-羟基嘧啶 硫酸盐
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关于此项目
经验公式（希尔记法）:
C4H7N5O · H2SO4
化学文摘社编号:
分子量:
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
存储类别
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
法规信息
新产品
此项目有
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
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