2,4-Di-tert-butylphenol

2,4-Di-tert-butylphenol
Names
Preferred IUPAC name
2,4-Di-tert-butylphenol
Other names
  • 2,4-Bis(1,1-dimethylethyl)phenol
  • 2,4-Bis(tert-butyl)phenol
  • 2,4-Di-tert-butylhydroxybenzene
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.002.303
EC Number
  • 202-532-0
UNII
  • InChI=1S/C14H22O/c1-13(2,3)10-7-8-12(15)11(9-10)14(4,5)6/h7-9,15H,1-6H3
    Key: ICKWICRCANNIBI-UHFFFAOYSA-N
  • CC(C)(C)c1ccc(O)c(c1)C(C)(C)C
Properties
C14H22O
Molar mass 206.329 g·mol−1
Appearance White crystalline solid
Odor phenolic, medical
Density 0.887
Melting point 56.8 °C (134.2 °F; 329.9 K)
Boiling point 264.2 °C (507.6 °F; 537.3 K)
33 mg/L at 25 °C, pH 6 - 7
Vapor pressure 5 Pa @ 38°C
Acidity (pKa) 11.6
Hazards
GHS labelling:
Warning
H315, H318, H410
P264, P273, P280, P302+P352, P305+P351+P338, P310, P332+P313, P362, P391, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

2,4-Di-tert-butylphenol (2,4-DTBP) is a white solid with a phenolic odour. It is primarily used as a raw material for the production of several commercially important antioxidants and phenolic benzotriazole-type UV absorbers. It also finds use as a starting material in the synthesis of agrochemicals, fragrances and catalysts (i.e. Jacobsen's catalyst).

Despite its toxicity against most tested organisms, it is made by a wide range of living organisms: 169 species of bacteria, fungi, plants, and animals.