Weight | 206.329 g/mol |
---|---|
Formula | C14H22O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
2,6-DI-TERT-BUTYLPHENOL (128-39-2)
2,6-di-tert-butylphenol, sodium salt · 2,6-bis(tert-butyl)phenol · 2,6-di-tert-butylphenol, potassium salt
Score:
#913 in Physics
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#2592 in Chemistry
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- Sigma-Aldrich - 2,6-DI-TERT-BUTYLPHENOL20.10 - 44.30 USD
- Fisher Scientific - Search for 2,6-DI-TERT-BUTYLPHENOL
- TCI - 2,6-DI-TERT-BUTYLPHENOL14.00 - 28.00 USD
- Reactions of 2,2-Methylenebis(4-chloro-6-isopropyl-3-methylphenol) and 2,2-Ethylidenebis(4,6-di-tert-butylphenol) with MgnBu2: Efficient Catalysts for Ring-Opening Polymerization of -Caprolactone and l-Lactide (Macromolecules, 2004)
- Chromatography of lipids in presence of an antioxidant, 4-methyl-2,6-di-tert.-butylphenol (Journal of Chromatography A, 1964)
- Autoxidation of 2,6-di-tert-butylphenol in water catalyzed by cobalt phthalocyaninetratrasulfonate bound to polymer colloids (Journal of Organic Chemistry, 1988)
- Aerial oxidation of primary alcohols and amines catalyzed by Cu(II) complexes of 2,2'-selenobis(4,6-di-tert-butylphenol) providing [O,Se,O]-donor atoms. (Dalton Transactions, 2004)
- Liquid-Phase Oxidation of 2,6-Di-tert-butylphenol with Cu-Impregnated MCM-41 Catalysts in the Presence of Alkali Metals (Journal of Catalysis, 1999)
- Oxidation of 2,6-di-tert-butylphenol with tert-butylhydroperoxide catalyzed by cobalt(II) phthalocyanine tetrasulfonate in a methanolwater mixture and formation of an unusual product 4,4-dihydroxy-3,3,5,5-tetra-tert-butylbiphenyl (Journal of Molecular Catalysis A-chemical, 2005)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2,6-di-tert-butylphenol, sodium salt
- 2,6-bis(tert-butyl)phenol
- 2,6-di-tert-butylphenol, potassium salt
- 2,6-di-t-butylphenol
-
SMILESCC(C)(C)C1=C(C(=CC=C1)C(C)(C)C)O
-
InChIKeyDKCPKDPYUFEZCP-UHFFFAOYSA-N
- Pubchem - 2,6-DI-TERT-BUTYLPHENOL
- Wikipedia - 2,6-di-tert-butylphenol
2,6-Di-tert-butylphenol is an organic compound with the structural formula 2,6-((CH3)3C)2C6H3OH. This colorless solid alkylated phenol and its derivatives are used industrially as UV stabilizers and antioxidants for hydrocarbon-based products ranging from petrochemicals to plastics. Illustrative of its usefulness, it prevents gumming in aviation fuels.
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