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B99405

Sigma-Aldrich

2-tert-Butylphenol

99%

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About This Item

Formula condensata:
(CH3)3CC6H4OH
Numero CAS:
88-18-6
Peso molecolare:
150.22
Beilstein:
1907120
Numero CE:
201-807-2
Numero MDL:
MFCD00002223
Codice UNSPSC:
12352100
ID PubChem:
24892164
NACRES:
NA.22

Tensione di vapore

0.05 mmHg ( 20 °C)

Livello qualitativo

100

Saggio

99%

Stato

liquid

Indice di rifrazione

n20/D 1.523 (lit.)

P. ebollizione

224 °C (lit.)

Punto di fusione

−7 °C (lit.)

Densità

0.978 g/mL at 25 °C (lit.)

Stringa SMILE

CC(C)(C)c1ccccc1O

InChI

1S/C10H14O/c1-10(2,3)8-6-4-5-7-9(8)11/h4-7,11H,1-3H3
WJQOZHYUIDYNHM-UHFFFAOYSA-N

Informazioni sul gene

mouse ... Esr1(13982)

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Categorie correlate

Avvertenze

Danger

Indicazioni di pericolo

H302 + H332,H311,H314,H411

Classi di pericolo

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

Codice della classe di stoccaggio

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

215.6 °F - Pensky-Martens closed cup

Punto d’infiammabilità (°C)

102 °C - Pensky-Martens closed cup

Dispositivi di protezione individuale

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
MKCQ3589
SHBK2668
SHBJ2252
SHBG5436V
SHBD7123V

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FLLL31 ≥98% (HPLC)

Sigma-Aldrich

F9057

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2-Propylphenol 98%

Sigma-Aldrich

P53608

2-Propylphenol

2-tert-Butylcyclohexanol, mixture of isomers 99%

Sigma-Aldrich

187828

2-tert-Butylcyclohexanol, mixture of isomers

A D Rahimtula et al.
British journal of cancer, 45(6), 935-944 (1982-06-01)
Six phenols [2(3)-t-butyl-4-hydroxyanisole (BHA), 2-t-butylphenol, 4-methoxyphenol, 4-methylmercaptophenol, t-butylhydroquinone and 2,6-di-t-butylphenol] previously shown to be inhibitors of benzo(a)pyrene-induced neoplasia, were examined for their ability to induce in vivo changes in hepatic mono-oxygenase and detoxication enzyme activities, and to act as mono-oxygenase
Zonglin Yang et al.
Journal of hazardous materials, 359, 203-212 (2018-07-24)
Nonylphenols (NPs) are known as Endocrine Disputing Chemicals (ECDs) and Persistent Organic Pollutants (POPs) and have attracted continuous attention. Biodegradation is one of the effective ways for pollutant removal in aquatic, sedimentary and soil environments. In this study, two estuarine
Andreas Meyer et al.
The Journal of biological chemistry, 277(7), 5575-5582 (2001-12-26)
The substrate reactivity of the flavoenzyme 2-hydroxybiphenyl 3-monooxygenase (EC, HbpA) was changed by directed evolution using error-prone PCR. In situ screening of mutant libraries resulted in the identification of proteins with increased activity towards 2-tert-butylphenol and guaiacol (2-methoxyphenol). One enzyme
Y Yasuda et al.
Microbiology and immunology, 28(11), 1203-1210 (1984-01-01)
Glucose interfered with the inhibitory action of hydrophobic compounds, such as n-octanol, diphenylamine and 2-tert-butylphenol, during L-alanine-initiated germination of Bacillus subtilis spores. The action of glucose on the action of the hydrophobic compounds was not competitive, and the binding affinity
Stefano Gabriele et al.
Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals, 19(6), 463-470 (2014-07-11)
The aromatic compound p-cresol (4-methylphenol) has been found elevated in the urines of Italian autistic children up to 8 years of age. The present study aims at replicating these initial findings in an ethnically distinct sample and at extending them
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