ALLOXAN MONOHYDRATE
Synonym(s):2,4,5,6(1H,3H)-Pyrimidinetetrone;2,4,5,6-Tetraoxypyrimidine;5,6-Dioxyuracil
- CAS NO.:2244-11-3
- Empirical Formula: C4H4N2O5
- Molecular Weight: 160.09
- MDL number: MFCD00149399
- EINECS: 607-078-0
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-12-18 14:15:30
What is ALLOXAN MONOHYDRATE?
Chemical properties
Off-white to beige-yellowish crystalline powder
The Uses of ALLOXAN MONOHYDRATE
A cytotoxic compound, Alloxan Monohydrate causes oxidative base damage to nuclear DNA.
The Uses of ALLOXAN MONOHYDRATE
specific cytotoxin (beta pacreatic cell)
The Uses of ALLOXAN MONOHYDRATE
Cytotoxic compound that causes oxidative base damage to nuclear DNAAlloxan monohydrate is used as a precursor to prepare purple dye murexide. It is also used in research models to induce diabetes and destroy beta cells. Further, it is a strong oxidizing agent and it forms a hemiacetal with its reduced reaction product dialuric acid.
What are the applications of Application
Alloxan monohydrate is a cytotoxic compound that causes oxidative base damage to nuclear DNA
Safety Profile
Poison by intravenous route. An experimental teratogen. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.
Purification Methods
Recrystallisation from H2O gave the tetrahydrate in large prisms or rhombs. On heating at 100o, or on exposure to air, this is converted to the monohydrate. Dissolve it in its own weight of boiling H2O and cool it for several days below 0o; the tetrahydrate crystallises from solution much more slowly when free from HNO3. It is less soluble in bicarbonate solutions than in H2O. Drying the solid over H2SO4 yields the monohydrate. The anhydrous crystals can be obtained by recrystallisation from dry Me2CO or AcOH followed by washing with dry Et2O, or by sublimation in a vacuum. On heating it turns pink at 230o and decomposes at ca 256o. It is acidic to litmus. [Hartman & Sheppard Org Synth Coll Vol III 37 1955.] It forms a compound with urea which crystallises from H2O in yellow needles that become red at 170o and decompose at 185-186o. [Beilstein 24 H 500, 24 I 428, 24 II 301, 24 III/IV 2137.]
Properties of ALLOXAN MONOHYDRATE
Melting point: | 255 °C (dec.)(lit.) |
storage temp. | 2-8°C |
solubility | H2O: may be hazy yellow |
form | Crystalline Powder |
color | Off-white to beige-yellow |
Water Solubility | Soluble in water, ethanol, acetone, glacial acetic acid and methanol. Slightly soluble in chloroform, petroleum ether, toluene, ethyl acetate and acetic anhydride. Insoluble in ether. |
Sensitive | Air Sensitive |
Merck | 14,282 |
BRN | 5309394 |
CAS DataBase Reference | 2244-11-3(CAS DataBase Reference) |
EPA Substance Registry System | 2,4,5,6(1H,3H)-Pyrimidinetetrone, monohydrate (2244-11-3) |
Safety information for ALLOXAN MONOHYDRATE
Signal word | Warning |
Pictogram(s) |
Exclamation Mark Irritant GHS07 |
Precautionary Statement Codes |
P261:Avoid breathing dust/fume/gas/mist/vapours/spray. P264:Wash hands thoroughly after handling. P264:Wash skin thouroughly after handling. P280:Wear protective gloves/protective clothing/eye protection/face protection. P301+P312:IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell. |
Computed Descriptors for ALLOXAN MONOHYDRATE
New Products
Tert-butyl bis(2-chloroethyl)carbamate 4-Methylphenylacetic acid N-Boc-D-alaninol N-BOC-D/L-ALANINOL N-octanoyl benzotriazole 3-Morpholino-1-(4-nitrophenyl)-5,6-dihydropyridin- 2(1H)-one Furan-2,5-Dicarboxylic Acid DIETHYL AMINOMALONATE HYDROCHLORIDE 1,1’-CARBONYLDIIMIDAZOLE R-2-BENZYLOXY PROPIONIC ACID 1,1’-CARBONYLDI (1,2-4 TRIAZOLE) N-METHYL INDAZOLE-3-CARBOXYLIC ACID (2-Hydroxyphenyl)acetonitrile 4-Bromopyrazole 5-BROMO-2CYANO PYRIDINE 5,6-Dimethoxyindanone 5-broMo-2-chloro-N-cyclopentylpyriMidin-4-aMine 2-(Cyanocyclohexyl)acetic acid 4-methoxy-3,5-dinitropyridine 1-(4-(aminomethyl)benzyl)urea hydrochloride 2-aminopropyl benzoate hydrochloride diethyl 2-(2-((tertbutoxycarbonyl)amino) ethyl)malonate tert-butyl 4- (ureidomethyl)benzylcarbamate Ethyl-2-chloro((4-methoxyphenyl)hydrazono)acetateRelated products of tetrahydrofuran
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