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447323
2,5-Di-tert-butyl-4-methoxyphenol
97%
Synonym(e):
2,5-Di-tert.-butyl-4-hydroxyanisol
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About This Item
Lineare Formel:
CH3OC6H2[C(CH3)3]2OH
CAS-Nummer:
Molekulargewicht:
236.35
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
Preise und Verfügbarkeit sind derzeit nicht verfügbar.
Empfohlene Produkte
Qualitätsniveau
Assay
97%
mp (Schmelzpunkt)
99-102 °C (lit.)
SMILES String
COc1cc(c(O)cc1C(C)(C)C)C(C)(C)C
InChI
1S/C15H24O2/c1-14(2,3)10-9-13(17-7)11(8-12(10)16)15(4,5)6/h8-9,16H,1-7H3
InChIKey
FLLRQABPKFCXSO-UHFFFAOYSA-N
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
dust mask type N95 (US), Eyeshields, Gloves
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Sensitive high-performance liquid chromatographic method for the routine determination of butylated hydroxyanisole in plasma.
H Verhagen et al.
Journal of chromatography, 413, 282-286 (1987-01-23)
Efficacy of solid acids in the synthesis of butylated hydroxy anisoles by alkylation of 4-methoxyphenol with MTBE.
Yadav GD and Rahuman MSMM.
Applied Catalysis A: General, 1, 113-123 (2003)
T Mizutani
Research communications in chemical pathology and pharmacology, 50(1), 125-133 (1985-10-01)
Dietary administration of butylated hydroxyanisole (BHA) and its analogs, 2-tert-butyl-1,4-dimethoxybenzene, 2,5-di-tert-butyl-4-methoxyphenol, and 2,6-di-tert-butyl-4-methoxyphenol resulted in complete protection against the lung toxicity of butylated hydroxytoluene (BHT) in mice. The protective effects of these compounds could not be accounted for by their
J Qu et al.
Biochimica et biophysica acta, 1501(2-3), 99-115 (2000-06-06)
Phosphatidylserine (PS) was exposed at the surface of human umbilical vein endothelial cells (HUVECs) and cultured cell lines by agonists that increase cytosolic Ca(2+), and factors governing the adhesion of T cells to the treated cells were investigated. Thrombin, ionophore
A Iwado et al.
Chemical & pharmaceutical bulletin, 48(11), 1831-1832 (2000-11-22)
Anion-exchange resins modified with metal-porphine (M-Pr) have been investigated to develop a solid catalyst in the oxidative reaction of phenols by O2 in air. Co-Pr, which is easily prepared and separable from the reaction mixture, has been proved to accelerate
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