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2,4-Dimethyl-6-tert-butylphenol

From Wikipedia, the free encyclopedia
2,4-Dimethyl-6-tert-butylphenol
Names
Preferred IUPAC name
2-tert-Butyl-4,6-dimethylphenol
Other names
2,4-Dimethyl-6-tert-butylphenol
6-tert-Butyl-2,4-dimethylphenol
2-(tert-Butyl)-4,6-dimethylphenol
2-tert-Butyl-4,6-dimethyl phenol
6-t-Butyl-2,4-xylenol
2-(1,1-Dimethylethyl)-4,6-dimethyl-phenol
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard100.015.940Edit this at Wikidata
EC Number
  • 217-533-1
UNII
UN number2430
  • InChI=1S/C12H18O/c1-8-6-9(2)11(13)10(7-8)12(3,4)5/h6-7,13H,1-5H3 checkY
    Key: OPLCSTZDXXUYDU-UHFFFAOYSA-N checkY
  • InChI=1/C12H18O/c1-8-6-9(2)11(13)10(7-8)12(3,4)5/h6-7,13H,1-5H3
    Key: OPLCSTZDXXUYDU-UHFFFAOYAT
  • CC(C)(C)c1c(O)c(C)cc(C)c1
  • Oc1c(cc(cc1C(C)(C)C)C)C
Properties
C12H18O
Melting point21 to 23 °C (70 to 73 °F; 294 to 296 K)
Boiling point248 to 249 °C (478 to 480 °F; 521 to 522 K)
Hazards
GHS labelling:
GHS06: ToxicGHS07: Exclamation markGHS08: Health hazardGHS09: Environmental hazard
Danger
H301,H302,H310,H315,H319,H373,H411
P260,P262,P264,P270,P273,P280,P301+P310,P301+P312,P302+P350,P302+P352,P305+P351+P338,P310,P314,P321,P322,P330,P332+P313,P337+P313,P361,P362,P363,P391,P405,P501
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

2,4-Dimethyl-6-tert-butylphenol is theorganic compound with the formula Me2(tert-Bu)C6H2OH (Me =methyl,tert-Bu = tertiary butyl). It is a colorless oil that is classified as analkylatedphenol.[1]

Preparation, reactions, uses

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It is used as anantioxidant, e.g. to prevent gumming infuels, and as an ultraviolet stabilizer. It is used injet fuels,gasolines, andavgas.

It is prepared by alkylation of xylenol withisobutylene. This alkylation provides a means to separate 2,4-xylenol from 2,5-xylenol since 2,4-dimethyl-6-tert-butylphenol is insoluble in 10% NaOH but 2,5-dimethyl-6-tert-butylphenol is soluble. Subsequent to separation, the tert-butyl group can be removed in strong acid.[1]

Tradenames

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One of its trade names isTopanol A. It is found in antioxidant mixtures AO-30, AO-31, AO-32, IONOL K72, IONOL K78, IONOL K98, and others.

See also

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References

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  1. ^abFiege H (2000). "Cresols and Xylenols".Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH.doi:10.1002/14356007.a08_025.ISBN 3-527-30673-0.
Fuel types
Fuel additives
Fluids
Retail
Food antioxidants
Fuel antioxidants
Measurements
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