447323
2,5-Di-tert-butyl-4-methoxyphenol
97%
Sinonimo/i:
2,5-Di-tert-butyl-4-hydroxyanisole
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About This Item
Formula condensata:
CH3OC6H2[C(CH3)3]2OH
Numero CAS:
Peso molecolare:
236.35
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
97%
Punto di fusione
99-102 °C (lit.)
Stringa SMILE
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
FLLRQABPKFCXSO-UHFFFAOYSA-N
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
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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