Nickel acetylacetonate

CAS: 3264-82-2

Ref. 3D-FN40503

Información del producto

• Nombre: Nickel acetylacetonate
• Sinónimos: (SP-4-1)-Bis(2,4-pentanedianato-kO,kO')nickel, (SP-4-1)-Bis(2,4-pentanedionato-κO²,κO⁴)nickel, Acetylacetonate, Nickel (Ii), Acetylacetonatonickel(II), Bis(2,4-pentanedionato)nickel, Bis(acetylacetonate)nickel, Bis(acetylacetonato)nickel, Bis(acetylacetone)nickel, Bis(pentan-2,4-dionato-O,O')nickel, Bis(pentane-2,4-dionato-O,O')nickel, Lc 5615, Nacem Nickel, Ni(acac)₂, Niax LC 5615, Nickel bis(2,4-pentanedionate), Nickel bis(acetylacetonate), Nickel(II) acetoacetonate, Nickel(II) acetylacetonate, Nickel(Ii)-Acetylacetonat, Nickel, Bis(2,4-Pentandionato-O,O')-, Nickel, bis(2,4-pentanedionato)-, Nickel, bis(2,4-pentanedionato-O,O')-, (SP-4-1)-, Nickel, bis(2,4-pentanedionato-κO2,κO4)-, (SP-4-1)-, Nickel, bis(2,4-pentanedionato-κO²,κO⁴)-, (SP-4-1)-, Nickelous acetylacetonate, Nsc 4657, bis(pentano-2,4-dionato-O,O')niquel
• CAS: 3264-82-2

Descripción

Nickel acetylacetonate is a biocompatible polymer that is used as an oxidation catalyst. It reacts with H2O2 to form hydroxyl radicals, which react with organic molecules and other compounds. Nickel acetylacetonate can be used in the chemical ionization process to measure the concentration of reactive oxygen species in aqueous solutions. The reaction mechanism of nickel acetylacetonate is similar to that of other metal-based catalysts such as platinum and palladium. This substance binds to the receptor site on the CCR5 protein on T lymphocytes, thereby inhibiting HIV infection. Nickel acetylacetonate has been shown to have a bound form and an unbound form. The unbound form is more reactive than the bound form due to its increased surface area for binding. The unbound form also has higher catalytic activity for hydrogen abstraction from water molecules or hydroxide ions than does the bound form.

• Marca: Biosynth

Propiedades químicas

• Peso molecular: 256.91 g/mol
• Fórmula: C₁₀H₁₄NiO₄
• Pureza: Min. 95%