3,3',5,5'-Tetra-tert-butyldiphenoquinone

CAS : 2455-14-3

Ref. 3D-FT32807

Informations sur le produit

• Nom: 3,3',5,5'-Tetra-tert-butyldiphenoquinone
• Synonymes: 2,5-Cyclohexadien-1-one, 4-[3,5-bis(1,1-dimethylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-2,6-bis(1,1-dimethylethyl)-, 2,6-Ditert-butyl-4-(3,5-ditert-butyl-4-oxocyclohexa-2,5-dien-1-ylidene)cyclohexa-2,5-dien-1-one, 3,3',5,5'-Tetra-Tert-Butyl-1,1'-Bi(Cyclohexa-2,5-Dien-1-Ylidene)-4,4'-Dione, 3,3',5,5'-Tetrabutyl-4,4'-Biphenylquinone, 3,3′,5,5′-Tetra-tert-butyl-4,4′-diphenoquinone, 3,3′,5,5′-Tetra-tert-butyldiphenoquinone, 3,5,3′,5′-Tetra-tert-butyldiphenoquinone, 3-(3,5-di-tert-butyl-4-oxocyclohexa-2,5-dien-1-ylidene)naphthalene-1,2,4(3H)-trione, 4-[3,5-Bis(1,1-dimethylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-2,6-bis(1,1-dimethylethyl)-2,5-cyclohexadien-1-one, Diphenoquinone, 3,3′,5,5′-tetra-tert-butyl-, NSC 14478, Tetra-tert-butyldiphenoquinone, [Bi-2,5-cyclohexadien-1-ylidene]-4,4′-dione, 3,3′,5,5′-tetra-tert-butyl-
• CAS: 2455-14-3

Description

3,3',5,5'-Tetra-tert-butyldiphenoquinone is a polymerized phenolic compound that is used as a dietary antioxidant. It has been shown to have hypochlorous and anion radical scavenging properties. It also acts as an oxidation catalyst and can be used for the preparation of oxidation products. 3,3',5,5'-Tetra-tert-butyldiphenoquinone stabilizes the formation of β-unsaturated aldehydes by acting as an oxidant. 3,3',5,5'-Tetra-tert-butyldiphenoquinone also has antioxidative activity by inhibiting lipid peroxidation in vitro. The antioxidant activity may be due to its ability to form hydrogen bonds with the lipid radicals produced during lipid peroxidation reactions.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 408.62 g/mol
• Formule: C₂₈H₄₀O₂
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C28H40O2/c1-25(2,3)19-13-17(14-20(23(19)29)26(4,5)6)18-15-21(27(7,8)9)24(30)22(16-18)28(10,11)12/h13-16H,1-12H3
• Code InChI: InChIKey=GQIGHOCYKUBBOE-UHFFFAOYSA-N
• SMILES: CC(C)(C)C1=CC(=C2C=C(C(C)(C)C)C(=O)C(C(C)(C)C)=C2)C=C(C(C)(C)C)C1=O