M6631
3-Methyluracil
Synonyme(s) :
3-MeU
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About This Item
Formule empirique (notation de Hill) :
C5H6N2O2
Numéro CAS:
Poids moléculaire :
126.11
Numéro MDL:
Code UNSPSC :
41106305
ID de substance PubChem :
Nomenclature NACRES :
NA.51
Produits recommandés
Essai
≥98% (TLC)
Niveau de qualité
Forme
powder
Solubilité
1 M NaOH: 50 mg/mL, clear, colorless to faintly yellow
Température de stockage
−20°C
Chaîne SMILES
CN1C(=O)NC=CC1=O
InChI
1S/C5H6N2O2/c1-7-4(8)2-3-6-5(7)9/h2-3H,1H3,(H,6,9)
Clé InChI
VPLZGVOSFFCKFC-UHFFFAOYSA-N
Description générale
3-Methyluracil is a methylated uracil or a uracil derivative.
Application
3-Methyluracil (3-MeU) is used along with other methyl-pyrimidines to study relative physical chemical parameters.
Mention d'avertissement
Warning
Mentions de danger
Conseils de prudence
Classification des risques
Carc. 2
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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T V Chestnova et al.
Bulletin of experimental biology and medicine, 165(6), 777-780 (2018-10-26)
Bacterial biofilms provoke and/or promote the most chronic and recurrent infectious diseases. Previously, experimental models of purulent peritonitis and meningoencephalitis revealed positive antibiofilm effect of metallic nanoparticles and the absence of resistance against such nanoparticles in microorganisms. This study examines
Vibrational Feshbach resonances in uracil and thymine.
Burrow PD, Gallup GA, et al.
J. Chem. Phys. , 28, 124310-124310 (2006)
A Nyéki et al.
British journal of clinical pharmacology, 55(1), 62-67 (2003-01-22)
(i) To compare the phenotyping of healthy subjects for NAT2 and CYP1A2 activities with caffeine, by the simultaneous assay of the urinary metabolites AFMU and AAMU, and (ii) to ascertain whether NAT2 and CYP1A2 phenotyping is influenced by the use
Mihajlo Etinski et al.
Physical chemistry chemical physics : PCCP, 12(19), 4915-4923 (2010-05-07)
In this work we investigated the lowest-lying electronic excitations for a series of methyl-substituted uracil derivatives, i.e., uracil, 1-methyluracil, 3-methyluracil, thymine, 1-methylthymine, 1,3-dimethyluracil, 3-methylthymine, 1,3-dimethylthymine, and their microhydrated complexes by means of coupled cluster singles and approximate doubles (CC2) and
S Fujita et al.
Radiation research, 114(2), 207-214 (1988-05-01)
Using a pulse radiolysis technique, some nucleic base radicals were produced by the reactions of sulfate radical, SO4-, with 1-, 3-, 5-, and 6-methyluracils, and their optical and kinetic natures were observed. All of their absorption spectra showed main peaks
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