5-hydroxyuracil structure
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Common Name | 5-hydroxyuracil | ||
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CAS Number | 496-76-4 | Molecular Weight | 128.086 | |
Density | 1.8±0.1 g/cm3 | Boiling Point | 534.5±53.0 °C at 760 mmHg | |
Molecular Formula | C4H4N2O3 | Melting Point | 300ºC | |
MSDS | Chinese USA | Flash Point | 277.0±30.9 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | 5-hydroxyuracil |
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Synonym | More Synonyms |
Density | 1.8±0.1 g/cm3 |
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Boiling Point | 534.5±53.0 °C at 760 mmHg |
Melting Point | 300ºC |
Molecular Formula | C4H4N2O3 |
Molecular Weight | 128.086 |
Flash Point | 277.0±30.9 °C |
Exact Mass | 128.022186 |
PSA | 85.95000 |
LogP | -2.10 |
Appearance of Characters | crystalline | light yellow |
Vapour Pressure | 0.0±1.5 mmHg at 25°C |
Index of Refraction | 1.719 |
Water Solubility | Soluble in DMSO (Sparingly), Methanol (Sparingly). |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi:Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
Hydrolytic pathway of 5-fluorouracil in aqueous solutions for clinical use.
J. Pharm. Biomed. Anal. 98 , 446-62, (2014) The purpose of the study was to investigate the degradation pathway of 5-fluorouracil (FU) in the situation of commercial formulations for clinical use, namely FU dissolved in sodium hydroxide (NaOH) ... |
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Mutational analysis of the damage-recognition and catalytic mechanism of human SMUG1 DNA glycosylase.
Nucleic Acids Res. 32(17) , 5291-302, (2004) Single-strand selective monofunctional uracil-DNA glycosylase (SMUG1), previously thought to be a backup enzyme for uracil-DNA glycosylase, has recently been shown to excise 5-hydroxyuracil (hoU), 5-h... |
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Base-promoted reaction of 5-hydroxyuracil derivatives with peroxyl radicals.
Org. Lett. 12(18) , 4130-3, (2010) Addition of millimolar amounts of a weak base (pyridines) dramatically accelerates the reaction with peroxyl radicals of two biologically relevant uracil derivatives, 5-hydroxyuracil (HU) and 5-hydrox... |
Pyrimidinetriol |
2,4,6-ThihydroxypyriMidine |
pyrimidine-2,4,5-triol |
Isobarbitursaeure |
2,4,5-pyrimidinetriol |
2,4(1H,3H)-Pyrimidinedione, 5-hydroxy- |
Isobarbituric Acid |
2,4,5-Trihydroxypyrimidine,5-Hydroxyuracil,Isobarbituric acid |
5-hydroxyuracil |
2,4,5-Trihydroxypyrimidine |
Fluorouracil impurity B |
5-hydroxyisouracil |
5-Hydroxypyrimidine-2,4(1H,3H)-dione |
5-Hydroxy-2,4(1H,3H)-pyrimidinedione |
TRIFLUOROACETIC ACID REAGENTPLUS |
EINECS 207-829-9 |
MFCD00082987 |
Isobarbituric acid (VAN) (8CI) |