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137731

Sigma-Aldrich

2,4-Di-tert-butylphenol

99%

Sinonimo/i:

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

Formula condensata:
[(CH3)3C]2C6H3OH
Numero CAS:
Peso molecolare:
206.32
Beilstein:
1910383
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

Tensione di vapore

1 mmHg ( 84.5 °C)

Livello qualitativo

Saggio

99%

Forma fisica

solid

P. eboll.

265 °C (lit.)

Punto di fusione

53-56 °C (lit.)

Solubilità

water: soluble 0.033 g/L at 25 °C

Stringa SMILE

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
ICKWICRCANNIBI-UHFFFAOYSA-N

Informazioni sul gene

human ... GABRA1(2554)

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Descrizione generale

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

Applicazioni

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.

Pittogrammi

CorrosionEnvironment

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

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

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

239.0 °F - closed cup

Punto d’infiammabilità (°C)

115 °C - closed cup

Dispositivi di protezione individuale

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
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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