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Merck
CN

20520

4-tert-Butylphenol

puriss., ≥99.0% (GC)

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About This Item

Linear Formula:
(CH3)3CC6H4OH
CAS Number:
98-54-4
Molecular Weight:
150.22
EC Number:
202-679-0
UNSPSC Code:
12352100
PubChem Substance ID:
329752008
Beilstein/REAXYS Number:
1817334
MDL number:
MFCD00002367

Key Documents

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vapor pressure

1 mmHg ( 70 °C)

grade

puriss.

assay

≥99.0% (GC)

bp

236-238 °C (lit.)

mp

96-101 °C (lit.), 98-101 °C

solubility

alcohol: soluble, cold water: very slightly soluble, diethyl ether: soluble

density

0.908 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)c1ccc(O)cc1

InChI

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

InChI key

QHPQWRBYOIRBIT-UHFFFAOYSA-N

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General description

The effect of 4-tert-butylphenol (BP) in a murine model of atopic dermatitis was studied.

Application

4-tert-Butylphenol was used as a model pollutant to study the degaradation of 4-tert-butylphenol in various conditions.

signalword

Danger

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Hazard Classifications

Aquatic Chronic 1 - ED ENV 1 - Eye Dam. 1 - Repr. 2 - Skin Irrit. 2

Regulatory Information

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Yanlin Wu et al.
The journal of physical chemistry. A, 118(2), 396-403 (2013-12-19)
The present work describes in detail the chemical structure of the complex Fe(III)–EDDS and the predominance of different species with respect to pH. These results were obtained with ab initio calculations. From the photoredox process, the formation of hydroxyl radical
Sonnich Meier et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 145(3), 420-430 (2007-03-09)
Offshore oil production releases large amounts of lipophilic compounds in produced water into the ocean. In 2004, 143 million m(3) produced water, containing approximately 13 tons of long-chain (>C(4)) alkylphenols (AP), was discharged from installations in the Norwegian sector of
Lei Lei et al.
Ecotoxicology (London, England), 19(7), 1268-1276 (2010-06-17)
Landfill leachates contain a large amount of unknown harmful compounds derived from domestic and industrial sources. A toxicity effect-directed approach was used to identify biologically active compounds in three landfill leachate samples (S1-S3) by combining the Microtox test with reverse-phase
Prashiela Manga et al.
The American journal of pathology, 169(5), 1652-1662 (2006-10-31)
Vitiligo presents with depigmented cutaneous lesions following localized melanocyte death. Multiple factors contribute to cell death, including genetically determined susceptibility to trauma, and environmental factors, such as exposure to 4-tert-butylphenol (4-TBP). We demonstrate that 4-TBP induces oxidative stress that is
Swarnalatha Kokatam et al.
Inorganic chemistry, 46(4), 1100-1111 (2007-02-13)
From the reaction of in situ generated 1,2-di(4-tert-butylphenyl)ethylene-1,2-dithiol, 2LH2, and Na[AuCl4].2H2O in 1,4-dioxane, green brown crystals of diamagnetic [N(n-Bu)4][AuIII(2L)2] (1) were obtained. As shown by cyclic voltammetry, 1 is a member of an electron-transfer series comprising the dianion [AuII(2L)2]2-, the
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