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137731

Sigma-Aldrich

2,4-Di-tert-butylphenol

99%

Synonym(s):

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

Linear Formula:
[(CH3)3C]2C6H3OH
CAS Number:
96-76-4
Molecular Weight:
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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Certificates of Analysis (COA)

Lot/Batch Number
BCCH0666
BCCF7172
BCCB3522
BCBX4597
BCBW8081

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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
Mee Kyung Sang et al.
Phytopathology, 101(6), 666-678 (2011-03-17)
We previously selected rhizobacterial strains CCR04, CCR80, GSE09, ISE13, and ISE14, which were antagonistic to Phytophthora blight of pepper. In this study, we investigated the effects of root treatment of rhizobacteria on anthracnose occurrence, ripening, and yield of pepper fruit
S Kalaichelvan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 85(1), 198-209 (2011-10-25)
In the present work, we reported a combined experimental and theoretical study on conformational stability, molecular structure and vibrational spectra of 2,4-di-tert-butylphenol (2,4-DTBP). The FT-IR (400-4000cm(-1)) and FT-Raman spectra (50-3500cm(-1)) of 2,4-DTBP were recorded. The molecular geometry, harmonic vibrational frequencies
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