Cas no 1088-56-8 (Lumiflavin)

Lumiflavin is a tricyclic heterocyclic compound derived from riboflavin (vitamin B2), specifically through the photodegradation of flavins. It serves as a key intermediate in the study of flavoprotein mechanisms and photochemical reactions. Lumiflavin exhibits strong fluorescence properties, making it valuable in spectroscopic and analytical applications. Its stability under controlled conditions allows for precise investigations into electron transfer processes and redox reactions. The compound is particularly useful in research involving flavin-dependent enzymes and photobiology. Lumiflavin's well-defined structure and reactivity profile make it a reliable reference standard in biochemical and photochemical studies. Its applications extend to probing enzymatic mechanisms and modeling natural photodegradation pathways.
Lumiflavin structure
Lumiflavin structure
Product Name:Lumiflavin
CAS No:1088-56-8
MF:C13H12N4O2
MW:256.25998210907
MDL:MFCD00042742
CID:188024
PubChem ID:66184
Update Time:2025-05-22

Lumiflavin Chemical and Physical Properties

Names and Identifiers

    • Benzo[g]pteridine-2,4(3H,10H)-dione,7,8,10-trimethyl-
    • LUMIFLAVINE
    • 7,8,10-trimethylbenzo[g]pteridine-2,4-dione
    • Lumiflavin
    • 7,8,10-Trimethyl-10H-benzo[g]pteridin-2,4-dion
    • 7,8,10-trimethyl-10H-benzo[g]pteridine-2,4-dione
    • 7,8,10-Trimethylbenzo(g)pteridine-2,4(3H,10H)-dione
    • 7,8,10-Trimethylisoalloxazine
    • EINECS 214-125-5
    • Lumilactoflavin
    • Lumiflavin (III)
    • Riboflavin EP Impurity A
    • Riboflavin Impurity 3 (Lumiflavine)
    • 7,8,10-trimethylbenzo[g]pteridine-2,4-quinone
    • (3h,10h)-dione,7,8,10-trimethyl-benzo(g)pteridine-4
    • BENZO(G)PTERIDINE-2,4(3H,10H)-DIONE, 7,8,10-TRIMETHYL-
    • KPDQZGKJTJRBGU-UHFFFAOYSA-
    • HY-121608
    • CHEBI:43661
    • 7,8,10-Trimethylbenzo(g)pteridine-2,4,(3H,10H)-dione
    • FT-0670872
    • J-002198
    • DB04726
    • BENZO(G)PTERIDIN-2(10H)-ONE, 4-HYDROXY-7,8,10-TRIMETHYL-
    • BDBM50362897
    • CCRIS 6316
    • RIBOFLAVIN IMPURITY A [EP IMPURITY]
    • CHEMBL1233985
    • KPDQZGKJTJRBGU-UHFFFAOYSA-N
    • Benzo[g]pteridine-2,4(3H,10H)-dione, 7,8,10-trimethyl-
    • NS00023508
    • InChI=1/C13H12N4O2/c1-6-4-8-9(5-7(6)2)17(3)11-10(14-8)12(18)16-13(19)15-11/h4-5H,1-3H3,(H,16,18,19)
    • LUMIFLAVINE [USP IMPURITY]
    • Q6703239
    • Benzo(g)pteridine-2,4,(3H,10H)-dione, 7,8,10-trimethyl-
    • 7,8,10-Trimethylbenzo[g]pteridine-2,4(3H,10H)-dione
    • 4M2669414M
    • 7,8,10-trimethyl-2H,3H,4H,10H-benzo[g]pteridine-2,4-dione
    • 1088-56-8
    • UNII-4M2669414M
    • AS-82190
    • RIBOFLAVIN SODIUM PHOSPHATE IMPURITY E [EP IMPURITY]
    • MFCD00042742
    • SCHEMBL193713
    • LUMIFLAVINE [MI]
    • DTXSID10148745
    • AKOS004910107
    • 7,8,10-Trimethylbenzo[g]pteridine-2,4(3H,10H)-dione #
    • MDL: MFCD00042742
    • Inchi: 1S/C13H12N4O2/c1-6-4-8-9(5-7(6)2)17(3)11-10(14-8)12(18)16-13(19)15-11/h4-5H,1-3H3,(H,16,18,19)
    • InChI Key: KPDQZGKJTJRBGU-UHFFFAOYSA-N
    • SMILES: O=C1C2C(=NC(N1)=O)N(C)C1C=C(C)C(C)=CC=1N=2

Computed Properties

  • Exact Mass: 256.09600
  • Monoisotopic Mass: 256.096
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 0
  • Complexity: 511
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: 3
  • XLogP3: nothing
  • Topological Polar Surface Area: 74.1A^2

Experimental Properties

  • Color/Form: powder
  • Density: 1.5±0.1 g/cm3
  • Melting Point: 320°; mp 330°
  • Boiling Point: Not available
  • Flash Point: Not available
  • Refractive Index: 1.728
  • Stability/Shelf Life: Stable. Incompatible with strong oxidizing agents.
  • PSA: 80.64000
  • LogP: 0.78680
  • Merck: 13,5621
  • Vapor Pressure: Not available

Lumiflavin Security Information

Lumiflavin Customs Data

  • HS CODE:2933990090
  • Customs Data:

    China Customs Code:

    2933990090

    Overview:

    2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Lumiflavin Pricemore >>

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Lumiflavin Related Literature

Additional information on Lumiflavin

Lumiflavin: A Comprehensive Overview

Lumiflavin, also known by its CAS number 1088-56-8, is a compound that has garnered significant attention in the scientific community due to its unique properties and versatile applications. This article delves into the latest research findings, providing an in-depth analysis of its characteristics, uses, and potential future developments.

The compound Lumiflavin is primarily recognized for its role in fluorescence and bioluminescence applications. Recent studies have highlighted its ability to act as a fluorescent probe in various biological systems. For instance, researchers have successfully utilized Lumiflavin in imaging techniques to monitor cellular processes with high precision. This advancement underscores its importance in modern biomedical research and diagnostics.

One of the most notable breakthroughs involving Lumiflavin is its application in sensing technologies. Scientists have developed sensors incorporating Lumiflavin to detect environmental pollutants with remarkable accuracy. These sensors leverage the compound's fluorescence properties to provide real-time monitoring of contaminants, making it a valuable tool in environmental protection and industrial safety.

In addition to its sensing capabilities, Lumiflavin has shown promise in drug delivery systems. Researchers have explored its potential as a carrier for therapeutic agents, thanks to its biocompatibility and ability to encapsulate drugs effectively. This innovative approach could revolutionize the way medications are administered, offering targeted delivery with minimal side effects.

The synthesis and structural characterization of Lumiflavin have also been subjects of extensive research. Recent advancements in synthetic methods have enabled the production of high-purity Lumiflavin, which is crucial for maintaining its efficacy in various applications. These methods include both traditional organic synthesis techniques and cutting-edge biotechnological approaches, ensuring a sustainable supply chain for this valuable compound.

Furthermore, the photophysical properties of Lumiflavin have been extensively studied to optimize its performance in different environments. By understanding how light interacts with the compound, researchers can tailor its applications to specific needs, such as enhancing fluorescence intensity or improving stability under varying conditions.

The integration of Lumiflavin into nanotechnology has opened new avenues for its use. Nanoparticles incorporating this compound have demonstrated enhanced performance in imaging and sensing applications, paving the way for next-generation nanotechnological solutions.

In conclusion, Lumiflavin, with its CAS number 1088-56-8, continues to be a focal point in scientific research due to its diverse applications and adaptability. As new studies emerge, the potential for this compound to contribute to advancements in medicine, environmental science, and technology remains vast and promising.

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