Substance

ID:181741

Names and Identifiers
IUPAC name
7,8-dimethyl-10-[(2S,3S,4R)-2,3,4,5-tetrahydroxypentyl]-2H,3H,4H,10H-benzo[g]pteridine-2,4-dione
IUPAC Traditional name
riboflavin
Synonyms
(-)-核黄素乳黄素(-)-Riboflavin维生素 G维生素 B2
Registration numbers
EC Number
MDL Number
CAS Number
Beilstein Number
PubChem SID
Properties
Product Information
Suitability
acrylamide photopolymerization tested
Foreign Activity
Protease, none detected
Physical Property
Melting Point
290 °C (dec.)(lit.)
Safety Information
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class
1
Molecule Details
Application
Riboflavin is suitable as a photopolymerization reagent in PAGE by forming free radicals in aqueous solution in the presence of light. Riboflavin photodecomposes to leucoflavin. No free radicals are formed in the absence of oxygen but traces of oxygen allows for leucoflavin to reoxidize with free-radical generation. The catalysts TEMED or DMAPN are commonly added to speed up the free radical formation. The free radicals will cause acrylamide and bis-acrylamide to polymerize to form a gel matrix which can be used for sieving macromolecules. Riboflavin is commonly used in the stacking gel for non-denaturing PAGE because native proteins can be sensitive to persulfate ions from ammonium persulfate. Another advantage of riboflavin over ammonium persulfate is that it will not start polymerizing until the gel is illuminated.
Molecular Spectra
No Data Available
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References
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