447323
2,5-Di-tert-butyl-4-methoxyphenol
97%
Synonym(s):
2,5-Di-tert-butyl-4-hydroxyanisole
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About This Item
Linear Formula:
CH3OC6H2[C(CH3)3]2OH
CAS Number:
Molecular Weight:
236.35
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
97%
mp
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
InChI key
FLLRQABPKFCXSO-UHFFFAOYSA-N
Related Categories
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
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)
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
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)
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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