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Merck
모든 사진(1)

문서

447323

Sigma-Aldrich

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

97%

동의어(들):

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 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


시험 성적서(COA)

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문서 라이브러리 방문

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)
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
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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