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Merck
CN

137731

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848346
EC Number:
202-532-0
Beilstein/REAXYS Number:
1910383
MDL number:
MFCD00008828

Key Documents

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Product Name

2,4-Di-tert-butylphenol, 99%

InChI key

ICKWICRCANNIBI-UHFFFAOYSA-N

InChI

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

SMILES string

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

vapor pressure

1 mmHg ( 84.5 °C)

assay

99%

form

solid

bp

265 °C (lit.)

mp

53-56 °C (lit.)

solubility

water: soluble 0.033 g/L at 25 °C

Quality Level

100

Gene Information

human ... GABRA1(2554)

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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.

General description

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

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

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
WXBF6344V
WXBF3855V
WXBF4460V
WXBF2339V
BCCJ1406

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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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