4-tert-Butylcatechol (98-29-3, 27213-78-1)

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  5 g
  $13.00

  100 g
  $30.00

  500 g
  $77.00

Most-cited Publications

• Mechanistic study of electrochemical oxidation of 4-tert-butylcatechol: A facile electrochemical method for the synthesis of new trimer of 4-tert-butylcatechol (Electrochimica Acta, 2004)
• Depigmentation from 4-Tertiary Butyl Catechol-An Experimental Study* (Journal of Investigative Dermatology, 1970)
• Calibration of a Clark-type oxygen electrode by tyrosinase-catalyzed oxidation of 4-tert-butylcatechol (Analytical Biochemistry, 1992)
• Electrochemical study of 3,4-dihydroxybenzoic acid and 4-tert-butylcatechol in the presence of 4-hydroxycoumarin application to the electro-organic synthesis of coumestan derivatives (Journal of Electroanalytical Chemistry, 1997)
• Structure and electronic properties of (N,N-bis(4-methyl-6-tert-butyl-2-methyl-phenolato)-N,N-bismethyl-1,2-diaminoethaneFeIII (DBSQ). Spectroelectrochemical study of the red-ox properties. Relevance to intradiol catechol dioxygenases (Inorganica Chimica Acta, 1997)
• Vapor Pressure, Heat Capacity, and Density along the Saturation Line, Measurements for Dimethyl Isophthalate, Dimethyl Carbonate, 1,3,5-Triethylbenzene, Pentafluorophenol, 4-tert-Butylcatechol, -Methylstyrene, and N,N-Bis(2-hydroxyethyl)ethylenediamine (Journal of Chemical & Engineering Data, 1997)

Areas of Application

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Trends

Alternate Names

• 4-tert-butyl catechol
• 4-tertiary butyl catechol
• p-tert-butyl catechol
• para-tert-butyl catechol
• SMILES
  CC(C)(C)C1=CC(=C(C=C1)O)O
• InChIKey
  XESZUVZBAMCAEJ-UHFFFAOYSA-N

External Links

• Pubchem - 4-tert-Butylcatechol
• Wikipedia - 4-tert-butylcatechol
  4-tert-Butylcatechol (TBC) is an organic chemical compound which is a derivative of catechol. It is added as a stabilizer and an inhibitor of polymerization to butadiene, styrene, vinyl acetate and other reactive monomer streams. It is 25 times better than hydroquinone at 60C for polymerization inhibitory effect.

Synthesis

Pyrocatechol  +  2-Chloro-2-methylpropane (Friedel-Crafts alkylation)

Synthesis of 4-tert-Butylcatechol ›

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4-tert-Butylcatechol

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