444-15-5

Basic information

• Product Name: DIALURIC ACID (100MGX5)
• Synonyms: 2,4,5,6-pyrimidinetetrol;2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-hydroxy-;5-hydroxy-2,4,6(1h,3h,5h)-pyrimidinetrione;5-hydroxy-barbituricaci;6(1h,3h,5h)-pyrimidinetrione,5-hydroxy-4;DIALURIC ACID (100MGX5);2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-hydroxy- (9CI);Dialuramic acid
• CAS NO: 444-15-5
• Molecular Formula: C₄H₄N₂O₄
• Molecular Weight: 144.08556
• EINECS: 207-145-0
• Product Categories: PYRIMIDINE;Heterocycles, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 444-15-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Density: 1.696 g/cm³
• Refractive Index: 1.551
• CAS DataBase Reference: DIALURIC ACID (100MGX5)(CAS DataBase Reference)
• NIST Chemistry Reference: DIALURIC ACID (100MGX5)(444-15-5)
• EPA Substance Registry System: DIALURIC ACID (100MGX5)(444-15-5)

Safety Data

• Hazardous Substances Data: 444-15-5(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 444-15-5 differently. You can refer to the following data:
1. Dialuric Acid is a metabolite of Alloxan.It is used for testing nutritional vitamin E status.
2. Dialuric acid is a metabolite of Alloxan. Dialuric acid is used for testing nutritional vitamin E status.

Definition

ChEBI: A member of the class of barbiturates that is barbituric acid in which a hydrogen attached to a ring carbon is replaced by a hydroxy group.

InChI:InChI=1/C4H4N2O4/c7-1-2(8)5-4(10)6-3(1)9/h1,7H,(H2,5,6,8,9,10)

Upstream product

• 3914-34-9 6-amino-5-hydroxy-1H-pyrimidine-2,4-dione 
• 61066-33-9 pyrimidine-2,4,5,6(1H,3H)-tetraone 
• 52-90-4 L-Cysteine 
• 99985-14-5 5-benzyloxy-barbituric acid 
• 302-01-2 hydrazine 
• 3683-34-9 cis-5,6-dihydroxydihydropyrimidine-2,4-dione 
• 7732-18-5 water 
• 10034-85-2 hydrogen iodide 
• 7647-01-0 hydrogenchloride 
• 23090-99-5 diazo-(5-hydroxy-2,4,6-trioxo-hexahydro-pyrimidin-5-yl)-acetic acid ethyl ester 
• 19186-12-0 dihydro-6-hydroxypyrimidine-2,4,5(3H)-trione 
• 64-19-7 acetic acid 
• 17356-08-0 thiourea 
• 76-24-4 Alloxantin 

Downstream Products

• 76-24-4 Alloxantin 
• 1780-40-1 2,4,5,6-tetrachloropyrimidine 
• 106-34-3 quinhydrone 
• 64-18-6 formic acid 
• 7664-41-7 ammonia 
• 476-61-9 [5,5']bipyrimidinyl-2,4,6,2',4',6'-hexaone 
• 15719-64-9 methylammonium carbonate 
• 1852-17-1 3,4,5,6-tetrahydropyrimidin-2(1H)-one 
• 122-78-1 phenylacetaldehyde 
• 124-38-9 carbon dioxide 
• 75-07-0 acetaldehyde 
• 118-78-5 uramil 
• 97-59-6 Allantoin 
• 80-69-3 tartronic acid 

Relevant articles and documents

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Selective Reduction by 2-Amino-4-methylpyridine Borane and 2-Aminopyrimidine Borane

Stereo- and chemoselective reductions and synthetic utility of the title compounds are described.

Reduction of Vicinal Tricarbonyl Compounds by Reduced Nicotinamide Adenine Dinucleotide Model and Electron-Transport Systems

The reduction of vicinal tricarbonyl compounds such as alloxan (A) and ninhydrin (NY) with 1-benzyl-1,4-dihydronicotinamide (BNAH; NADH model) was investigated.In the reduction of A with BNAH, the radical anion (A-.Py+) of A as the 1-benzyl-3-carbamoylpyridinium salt and the dialuric acid (D) was obtained by one-electron and two-electron reduction,respectively.Similarly,hydrindantin (HDT) and 2-hydroxy-1,3-indandione (HID) were also afforded in the reduction of NY with BNAH.Further,the reductions of alloxantin (AT) and HDT with BNAH were performed to give D and HID,respectively.The reduction of lipoic acid (LA) and viologens (V2+) with BNAH, which could not be reduced without A or NY, proceeded smoothly in their presence,and they proved to be useful as mediators for catalytic reduction of LA and V2+.