4-tert-Butylcatechol
Space-filling model of the 4-tert-butylcatechol molecule
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)
Abbreviations TBC
ChEMBL
ChemSpider
ECHA InfoCard 100.002.413
UNII
  • InChI=1S/C10H14O2/c1-10(2,3)7-4-5-8(11)9(12)6-7/h4-6,11-12H,1-3H3 checkY
    Key: XESZUVZBAMCAEJ-UHFFFAOYSA-N checkY
  • 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).
checkY verify (what is checkY☒N ?)
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]

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.

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

See also

References

  1. ↑ "Nomination Background: p-tert butylcatechol" (PDF). Nomination Background: p-tert butylcatechol. April 1993. Archived (PDF) from the original on 2017-01-31. 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. Archived (PDF) from the original on 2020-09-15. Retrieved 2020-09-04.
  6. ↑ "DuPont Divinylbenzene (TM) Technical Manual" (PDF). 2020-03-01. Archived (PDF) from the original on 2020-09-15. 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

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.