Azobenzene

CAS No. 103-33-3

Azobenzene( NSC 2102 | NSC-2102 | NSC2102 | Azobenzene )

Catalog No. M10162 CAS No. 103-33-3

Azobenzene is a chemical compound composed of two phenyl rings linked by a N=N double bond.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
500MG 35 In Stock
1G 42 In Stock

Biological Information

  • Product Name
    Azobenzene
  • Note
    Research use only, not for human use.
  • Brief Description
    Azobenzene is a chemical compound composed of two phenyl rings linked by a N=N double bond.
  • Description
    Azobenzene is a chemical compound composed of two phenyl rings linked by a N=N double bond. It is the simplest example of an aryl azo compound. The term 'azobenzene' or simply 'azo' is often used to refer to a wide class of molecules that share the core azobenzene structure, with different chemical functional groups extending from the phenyl rings.
  • In Vitro
    Photochromic compounds that undergo large conformational changes when exposed to light of appropriate wavelength are particularly attractive as molecular switch elements. Azobenzene is a popular choice among the chromophores. The thermodynamically favored trans isomer is rapidly converted to the cis isomer by irradiation at the wavelength of the π-π* transition, whereas the reverse process is achieved either (slowly) by thermal relaxation in the dark or (quickly) by irradiation at the wavelength of the n-π* transition. The azobenzene amino acid (aa) can be used as a photo-inducible conformational switch in polypeptides. A reversible conformational change of the peptide backbone is induced by switching between the cis and trans configurations of the azobenzene moiety by irradiation with light of suitable wavelength. Azobenzene has been the most widely used optical trigger for the synthesis of photoresponsive systems ranging from poly-a-amino acids to innovative materials with light-controlled mechanical and optical properties. Its use in form of appropriate derivatives allow to generate cyclic peptide structures of constraint conformational space and thus to exploit its reversible photoisomerization to induce well defined transitions between different conformational states. Azobenzene photoswitches can be used to drive functional changes in peptides, proteins, nucleic acids, lipids, and carbohydrates.
  • In Vivo
    ——
  • Synonyms
    NSC 2102 | NSC-2102 | NSC2102 | Azobenzene
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    103-33-3
  • Formula Weight
    182.22
  • Molecular Formula
    C12H10N2
  • Purity
    >98% (HPLC)
  • Solubility
    Water: 6.4 mg/L
  • SMILES
    C1(/N=N/C2=CC=CC=C2)=CC=CC=C1
  • Chemical Name
    Diazene, 1,2-diphenyl-

Shipping & Storage Information

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

Reference

1.Wu L, et al. Bioconjug Chem. 2015 Jun 17;26(6):1070-9.
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