L3307
Lumazine
97%
Synonym(s):
2,4(1H,3H)-Pteridinedione, 2,4-Dihydroxypteridine, 2,4-Pteridinediol
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About This Item
Empirical Formula (Hill Notation):
C6H4N4O2
CAS Number:
Molecular Weight:
164.12
EC Number:
207-652-7
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
157503
MDL number:
InChI key
UYEUUXMDVNYCAM-UHFFFAOYSA-N
InChI
1S/C6H4N4O2/c11-5-3-4(8-2-1-7-3)9-6(12)10-5/h1-2H,(H2,8,9,10,11,12)
SMILES string
Oc1nc(O)c2nccnc2n1
assay
97%
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Na'il Saleh et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 68(3), 728-733 (2007-03-31)
6-Thienyllumazine (TLM) is synthesized as a new fluorescent sensor that is capable of indicating selectively the presence of Cd(2+) ion via a fluorescence signal. Experiment has been performed in the presence of Ni(2+), Co(2+), Cu(2+), Ag(+), Mn(2+), Hg(2+), Zn(2+), Pb(2+)
M S Ibrahim et al.
Journal of pharmaceutical and biomedical analysis, 28(2), 217-225 (2002-04-04)
The interaction of lumazine, an antibacterial drug, with alpha-, beta-cyclodextrins and DNA in aqueous solution was studied by differential pulse stripping voltammetry and cyclic voltammetry as well as UV-vis spectroscopy. The electrochemical and absorption spectral data indicated a 1:1 complex
Xiaofeng Zhang et al.
Journal of molecular biology, 328(1), 167-182 (2003-04-10)
6,7-Dimethyl-8-ribityllumazine is the biosynthetic precursor of riboflavin, which, as a coenzyme, plays a vital role in the electron transfer process for energy production in all cellular organisms. The enzymes involved in lumazine biosynthesis have been studied in considerable detail. However
A E West et al.
Microbial ecology, 43(4), 408-415 (2002-06-04)
Experiments were done to test the hypothesis that atmospheric CH(4) oxidizers in a well-drained alpine tundra soil are supported by CH(4) production from anaerobic microsites in the soil. Soil was subjected to 22 days of anaerobic conditions with elevated H(2)
Cosima D Calvano et al.
Analytical and bioanalytical chemistry, 398(1), 499-507 (2010-07-02)
Nowadays, matrix-assisted laser desorption/ionization (MALDI) time-of-flight mass spectrometry represents an emerging and versatile tool for analysis of lipids. However, direct (i.e., with no previous separation of lipid classes) analysis of crude extracts containing a complex mixture of lipids (a problem
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