4-tert-Butylcatechol

Last updated
4-tert-Butylcatechol
Tert-butylcatechol Structural Formula V1.svg
4-tert-Butylcatechol-3D-spacefill.png
Names
Preferred IUPAC name
4-tert-Butylbenzene-1,2-diol
Other names
para-tert-Butylcatechol
p-tert-Butylcatechol
t-Butyl catechol
p-t-Butylpyrocatechol
p-tert-Butylpyrocatechol
4-t-Butylpyrocatechol
4-tert-Butylpyrocatechol
Identifiers
3D model (JSmol)
AbbreviationsTBC
ChEMBL
ChemSpider
ECHA InfoCard 100.002.413 OOjs UI icon edit-ltr-progressive.svg
PubChem CID
UNII
  • InChI=1S/C10H14O2/c1-10(2,3)7-4-5-8(11)9(12)6-7/h4-6,11-12H,1-3H3 Yes check.svgY
    Key: XESZUVZBAMCAEJ-UHFFFAOYSA-N Yes check.svgY
  • InChI=1/C10H14O2/c1-10(2,3)7-4-5-8(11)9(12)6-7/h4-6,11-12H,1-3H3
    Key: XESZUVZBAMCAEJ-UHFFFAOYAR
  • Oc1ccc(cc1O)C(C)(C)C
Properties
C10H14O2
Molar mass 166.217 g/mol
Melting point 50 °C
Boiling point 285 °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

4-tert-Butylcatechol (TBC) is an organic chemical compound which is a derivative of catechol. [1] TBC is available in the form of a solid crystal flake [2] and 85% solution in methanol [3] or water. [4]

Contents

Uses

It is added as a stabilizer and polymerisation inhibitor to butadiene, styrene, [5] vinyl acetate, divinylbenzene [6] and other reactive monomer streams. [7]

TBC is also used as a stabilizer in the manufacture of polyurethane foam. [8] It also can be used as an antioxidant for synthetic rubber, polymers and oil derivatives. [7] It can be used as purification agent for aminoformate catalysts.[ citation needed ]

It is 25 times better than hydroquinone at 60 °C for polymerization inhibitory effect.[ citation needed ]

See also

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References

  1. "Nomination Background: p-tert butylcatechol" (PDF). Nomination Background: p-tert butylcatechol. April 1993. Retrieved 4 September 2020.
  2. "TBC OPTIMA 100% FLAKES". Solvay. Retrieved 2020-09-04.
  3. "TBC OPTIMA 85% METHANOL". Solvay. Retrieved 2020-09-04.
  4. "TBC OPTIMA 85% WATER". Solvay. Retrieved 2020-09-04.
  5. "Styrene Safe Handling and Storage Guide" (PDF). Americas Styrenics. Retrieved 2020-09-04.
  6. "DuPont Divinylbenzene (TM) Technical Manual" (PDF). 2020-03-01. Retrieved 2020-09-04.
  7. 1 2 "4-Tertiary Butylcatechol | Business & Products". DIC Corporation. Retrieved 2020-09-04.
  8. "tert-Butylcatechol (TBC)". Silver Fern Chemical Inc. Retrieved 2020-09-04.

Sources