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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

Certificates of Analysis (COA)

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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
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
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
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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