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Documentos Principais

447323

Sigma-Aldrich

2,5-Di-tert-butyl-4-methoxyphenol

97%

Sinônimo(s):

2,5-Di-tert-butyl-4-hydroxyanisole

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About This Item

Fórmula linear:
CH3OC6H2[C(CH3)3]2OH
Número CAS:
Peso molecular:
236.35
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Ensaio

97%

pf

99-102 °C (lit.)

cadeia de caracteres SMILES

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

chave InChI

FLLRQABPKFCXSO-UHFFFAOYSA-N

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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
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)
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)
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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