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B99405

Sigma-Aldrich

2-tert-Butylphenol

99%

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About This Item

Linear Formula:
(CH3)3CC6H4OH
CAS Number:
88-18-6
Molecular Weight:
150.22
Beilstein:
1907120
EC Number:
201-807-2
MDL number:
MFCD00002223
UNSPSC Code:
12352100
PubChem Substance ID:
24892164
NACRES:
NA.22

vapor pressure

0.05 mmHg ( 20 °C)

Assay

99%

form

liquid

refractive index

n20/D 1.523 (lit.)

bp

224 °C (lit.)

mp

−7 °C (lit.)

density

0.978 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)c1ccccc1O

InChI

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

InChI key

WJQOZHYUIDYNHM-UHFFFAOYSA-N

Gene Information

mouse ... Esr1(13982)

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Related Categories

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 2

Flash Point(F)

215.6 °F - Pensky-Martens closed cup

Flash Point(C)

102 °C - Pensky-Martens closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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
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
Nunna V Krishna et al.
Dalton transactions (Cambridge, England : 2003), 46(3), 770-779 (2016-12-21)
Acid-mediated synthesis of ordered mesoporous aluminosilicates (OMAS) with medium-to-strong Brønsted acid sites and trivalent aluminium exclusively in a tetrahedral framework structure is realized by a newly devised intrinsic hydrolysis method. In this way, we have synthesized a series of well-ordered
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
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