4-tert-Butylpyrocatechol - 85% solution in methanol

CAS: 98-29-3

Ref. 3D-FT172778

Produktinformation

• Name: 4-tert-Butylpyrocatechol - 85% solution in methanol
• Synonyme: 1,2-Benzenediol, 4-(1,1-dimethylethyl)-, 1,2-Dihydroxy-4-tert-butylbenzene, 4-(1,1-Dimethylethyl)-1,2-benzenediol, 4-(1,1-Dimethylethyl)benzene-1,2-diol, 4-(1,1-Dimethylethyl)catechol, 4-Tbc, 4-Terc-Butilpirocatecol, 4-Tert-Butylbenzene-1,2-Diol, 4-tert-Butyl Pyrocatechol, 4-tert-Butyl-1,2-benzenediol, 4-tert-Butyl-1,2-dihydroxybenzene, 4-tert-Butyl-o-catechol, 4-tert-Butylbrenzcatechin, 4-tert-Butylcatechin, 4-tert-Butylcatechol solution, 4-tert-Butylpyrocatechol, 5-tert-Butylcatechol, Butylcatechol, Catechol, 4-Tert-Butyl-, Catechol, 4-Tertiary-Butyl, Inhibitor NLC 10, Nlc 10, Norpol 9853, Norpol Inhibitor 9853, Nsc 5310, Pyrocatechol, 4-tert-butyl-, TBC, Tris(2,3-Dibromopropyl-1)Isocyanurate, p-t-Butylcatechol, p-tert-Butylcatechol, p-tert-Butylpyrocatechol
• CAS: 98-29-3

Beschreibung

4-tert-Butylpyrocatechol is a glycol ester that is a byproduct of the synthesis of methyl ethyl ketone. It has been shown to have biochemical properties and can be used as an experimental model for the study of transfer reactions in organic solvents. The reaction mechanism of 4-tert-butylpyrocatechol is not well known, but it has been shown to react with bacterial strain and produce reactive intermediates during toxicity studies. 4-tert-Butylpyrocatechol can also be used for wastewater treatment due to its ability to catalyze oxidation reactions. The use of preparative high performance liquid chromatography (prep HPLC) enables the separation and purification of 4-tert-butylpyrocatechol from other compounds in solution. This method allows for kinetic studies on the enzyme activities of 4-tert-butylpyrocatechol.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 166.22 g/mol
• Formel: C₁₀H₁₄O₂
• Reinheit: Min. 95%
• InChl: InChI=1S/C10H14O2/c1-10(2,3)7-4-5-8(11)9(12)6-7/h4-6,11-12H,1-3H3
• InChI Key: InChIKey=XESZUVZBAMCAEJ-UHFFFAOYSA-N
• SMILES: CC(C)(C)c1ccc(O)c(O)c1