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Key Documents

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B99405

Sigma-Aldrich

2-tert-Butylphenol

99%

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About This Item

Fórmula lineal:
(CH3)3CC6H4OH
Número de CAS:
88-18-6
Peso molecular:
150.22
Beilstein/REAXYS Number:
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)

Quality Level

100

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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signalword

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

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

wgk_germany

WGK 2

flash_point_f

215.6 °F - Pensky-Martens closed cup

flash_point_c

102 °C - Pensky-Martens closed cup

ppe

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

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Certificados de análisis (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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