Lumiflavin

Base Information

• Chemical Name: Lumiflavin
• CAS No.: 1088-56-8
• Molecular Formula: C13H12 N4 O2
• Molecular Weight: 256.264
• Hs Code.: 2933990090
• European Community (EC) Number: 214-125-5
• UNII: 4M2669414M
• DSSTox Substance ID: DTXSID10148745
• Nikkaji Number: J7.251F,J1.763.593J
• Wikipedia: Lumiflavin
• Wikidata: Q6703239
• Metabolomics Workbench ID: 52345
• ChEMBL ID: CHEMBL1233985
• Mol file: 1088-56-8.mol

Synonyms:lumiflavin

Chemical Property of Lumiflavin

Chemical Property:

• Appearance/Colour: deep yellow powder
• Melting Point: 320°; mp 330°
• Boiling Point: °Cat760mmHg
• PKA: 10.05±0.70(Predicted)
• Flash Point: °C
• PSA: 80.64000
• Density: 1.47g/cm³
• LogP: 0.78680
• Storage Temp.: 2-8°C
• Solubility.: Methanol (Very Slightly, Heated, Sonicated), Trifluoroacetic Acid (Very Slightly
• XLogP3: 1.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 256.09602564
• Heavy Atom Count: 19
• Complexity: 511

Purity/Quality:

98%,99%, ^*data from raw suppliers

Lumiflavin ^*data from reagent suppliers

Safty Information:

• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC2=C(C=C1C)N(C3=NC(=O)NC(=O)C3=N2)C
• Uses: Lumiflavin is a toxic photolysis product of vitamin B2 (R415000).

Technology Process of Lumiflavin

There total 29 articles about Lumiflavin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

water (7732-18-5) + flavin adenine dinucleotide (146-14-5,887565-61-9) → lumiflavin (1088-56-8) + 5'-adenosine monophosphate (61-19-8,24937-83-5,67583-85-1) + Flavin mononucleotide (146-17-8,69680-01-9) + riboflavin (83-88-5,42880-33-1)

Guidance literature:

vom pH 3-9;

Reference yield:

hydrogenchloride (7647-01-0,15364-23-5) + flavin adenine dinucleotide (146-14-5,887565-61-9) → lumiflavin (1088-56-8) + 5'-adenosine monophosphate (61-19-8,24937-83-5,67583-85-1) + Flavin mononucleotide (146-17-8,69680-01-9) + riboflavin (83-88-5,42880-33-1)

Guidance literature:

Adenin, O⁵-Phosphono-D-ribose und H₃PO₄;

Reference yield:

Flavin mononucleotide (146-17-8,69680-01-9) → lumiflavin (1088-56-8) + riboflavin (83-88-5,42880-33-1)

Guidance literature:

mit sichtbares oder ultraviolettes Licht_.Irradiation;

upstream raw materials:

BARBITURIC ACID

4-(4,5-dimethyl-2-methylamino-phenylazo)-benzoic acid

4,5,N-trimethyl-2-(4-nitro-phenylazo)-aniline

pyrimidine-2,4,5,6(1H,3H)-tetraone

Downstream raw materials:

(7,8,10-trimethyl-2,4-dioxo-4,10-dihydro-2H-benzo[g]pteridin-3-yl)-acetic acid ethyl ester

(7,8,10-trimethyl-2,4-dioxo-4,10-dihydro-2H-benzo[g]pteridin-3-yl)acetic acid

2,3,4,5,6-pentafluorophenyl 2-(5,7,8-trimethyl-1,3-dioxo-2,5-dihydro-2,4-diazaphenazin-2-yl)acetate

Ro 08-2750

Refernces

• 1、 Nanni, Edward J.,Sawyer, Donald T.. "Superoxide-Ion Oxidation of Hydrophenazines, Reduced Flavins, Hydroxylamine, and Related Substrates via Hydrogen-Atom Transfer". . p. 7591 - 7593. Retrieved 1980.
• 2、 Xu, Jia,Birke, Ronald L.,Lombardi, John R.. "Surface-Enhanced Raman Spectroscopy from Flavins Adsorbed on a Silver Electrode: Observation of the Unstable Semiquinone Intermediate". . p. 5645 - 5649. Retrieved 1987.
• 3、 Ahmad, Iqbal,Mirza, Tania,Musharraf, Syed Ghulam,Anwar, Zubair,Sheraz, Muhammad Ali,Ahmed, Sofia,Ejaz, Muhammad Ahsan,Khurshid, Adeela. "Photolysis of carboxymethylflavin in aqueous and organic solvent: A kinetic study". . p. 26559 - 26571. Retrieved 2019/09/06.
• 4、 -. "Light activated composite tissue adhesives". Page/Page column 1. . Retrieved 2015/04/28.