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Benzophenonetetracarboxylic acid

CAS No. 2479-49-4

Benzophenonetetracarboxylic acid( —— )

Catalog No. M33590 CAS No. 2479-49-4

Benzophenonetetracarboxylic acid (3,3',4,4'-Benzophenonetetracarboxylic acid) is utilized in the preparation of high-performance polyimides and serves as a curing agent for epoxy resins.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
10MG 28 Get Quote
25MG 40 Get Quote
50MG 53 Get Quote
100MG 79 Get Quote
500MG 199 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Benzophenonetetracarboxylic acid
  • Note
    Research use only, not for human use.
  • Brief Description
    Benzophenonetetracarboxylic acid (3,3',4,4'-Benzophenonetetracarboxylic acid) is utilized in the preparation of high-performance polyimides and serves as a curing agent for epoxy resins.
  • Description
    Benzophenonetetracarboxylic acid (3,3',4,4'-Benzophenonetetracarboxylic acid) is particularly useful in the preparation of high performance polyimides and also useful as curing agents for epoxy resins.
  • In Vitro
    The kinetics of the photooxidation of aromatic amino acids histidine (His), tyrosine (Tyr), and tryptophan (Trp) by Benzophenonetetracarboxylic acid has been investigated in aqueous solutions using time-resolved laser flash photolysis and time-resolved chemically induced dynamic nuclear polarization. The pH dependence of quenching rate constants is measured within a large pH range. The chemical reactivities of free His, Trp, and Tyr and of their acetylated derivatives, N-AcHis, N-AcTyr, and N-AcTrp, toward Benzophenonetetracarboxylic acid triplets are compared to reveal the influence of amino group charge on the oxidation of aromatic amino acids. Thus, it has been established that the presence of charged amino group changes oxidation rates by a significant factor; i.e., His with a positively charged amino group quenches the Benzophenonetetracarboxylic acid triplets 5 times more effectively than N-AcHis and His with a neutral amino group. The efficiency of quenching reaction between the Benzophenonetetracarboxylic acid triplets and Tyr and Trp with a positively charged amino group is about 3 times as high as that of both Tyr and Trp with a neutral amino group, N-AcTyr and N-AcTrp.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2479-49-4
  • Formula Weight
    358.26
  • Molecular Formula
    C17H10O9
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (139.56 mM; Ultrasonic )H2O : 10 mg/mL (27.91 mM; Ultrasonic)
  • SMILES
    C(=O)(C1=CC(C(O)=O)=C(C(O)=O)C=C1)C2=CC(C(O)=O)=C(C(O)=O)C=C2
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Mengxian Ding, et al. Process for the preparation of 3,3',4,4'-biphenyltetracarboxylic acid and its derivatives. Jan. 14, 1992. US5081281A.
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