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137731

Sigma-Aldrich

2,4-Di-tert-butylphenol

99%

Sinónimos:

2,4-Bis(1,1-dimethylethyl)phenol, 2,4-Bis(tert-butyl)phenol, 2,4-Di-tert-butylhydroxybenzene, 2,4-Ditert-butylphenol

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About This Item

Fórmula lineal:
[(CH3)3C]2C6H3OH
Número de CAS:
96-76-4
Peso molecular:
206.32
Beilstein/REAXYS Number:
1910383
EC Number:
202-532-0
MDL number:
MFCD00008828
UNSPSC Code:
12352100
PubChem Substance ID:
24848346
NACRES:
NA.22

vapor pressure

1 mmHg ( 84.5 °C)

Quality Level

100

assay

99%

form

solid

bp

265 °C (lit.)

mp

53-56 °C (lit.)

solubility

water: soluble 0.033 g/L at 25 °C

SMILES string

CC(C)(C)c1ccc(O)c(c1)C(C)(C)C

InChI

1S/C14H22O/c1-13(2,3)10-7-8-12(15)11(9-10)14(4,5)6/h7-9,15H,1-6H3

InChI key

ICKWICRCANNIBI-UHFFFAOYSA-N

Gene Information

human ... GABRA1(2554)

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General description

2,4-Di-tert-butylphenol is isolated from the dried body of Scolopendra and possess antioxidative activity.

Application

2,4-Di-tert-butylphenol was used to study its alkylation reaction with cinnamyl alcohol in the presence of Al-substituted disordered hexagonal molecular silica catalysts.

pictograms

CorrosionEnvironment
GHS05,GHS09

signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 2

flash_point_f

239.0 °F - closed cup

flash_point_c

115 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Sherry Cox et al.
PeerJ, 5, e3476-e3476 (2017-07-05)
Propofol is an intravenous anesthetic commonly used due to its favorable pharmacokinetic and pharmacodynamic profile. There are discrepancies in the literature about the most appropriate sample for determining propofol concentrations. Although plasma has been used for determining propofol concentrations, whole
Textural mesoporosity and the catalytic activity of mesoporous molecular sieves with wormhole framework structures.
Pauly TR, et al.
Journal of the American Chemical Society, 121(38), 8835-8842 (1999)
Jae Kwak et al.
PloS one, 11(3), e0151474-e0151474 (2016-03-12)
Male house mice produce large quantities of major urinary proteins (MUPs), which function to bind and transport volatile pheromones, though they may also function as scavengers that bind and excrete toxic compounds ('toxic waste hypothesis'). In this study, we demonstrate
Verónica Ramírez et al.
Frontiers in microbiology, 11, 741-741 (2020-05-20)
Volatile organic compounds (VOCs) produced by rhizobacteria have been proven to stimulate plant growth during germination and seedling stages. However, the modulating effect of bacterial volatiles on the germination of seeds subjected to heavy metal stress is scarcely studied. In
M K Sang et al.
Journal of applied microbiology, 113(2), 383-398 (2012-05-09)
Previously, we selected a bacterial strain (GSE09) antagonistic to Phytophthora capsici on pepper, which produced a volatile compound (2,4-di-tert-butylphenol), inhibiting the pathogen. In this study, we identified strain GSE09 and characterized some of the biological traits of this strain in
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