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Merck
CN

W391808

4-叔丁基苯酚

≥99%, FG

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线性分子式:
(CH3)3CC6H4OH
化学文摘社编号:
分子量:
150.22
Flavis number:
4.064
PubChem Substance ID:
UNSPSC Code:
12164502
FEMA Number:
3918
EC Number:
202-679-0
MDL number:
Beilstein/REAXYS Number:
1817334
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biological source

synthetic

grade

FG

reg. compliance

EU Regulation 1334/2008 & 872/2012

vapor pressure

1 mmHg ( 70 °C)

assay

≥99%

bp

236-238 °C (lit.)

mp

96-101 °C (lit.)

solubility

ethanol: 50 mg/mL, clear, colorless

density

0.908 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

leather

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

Gene Information

mouse ... Esr1(13982)
rat ... Ar(24208)

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General description

4-tert-Butylphenol is an alkylphenolic compound that can be used as a flavoring agent. It is also a component of adhesives and polymers used for food packaging.

signalword

Danger

Hazard Classifications

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

存储类别

13 - Non 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

法规信息

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Zhigang Xu et al.
Journal of chromatography. A, 1358, 52-59 (2014-07-20)
In this study, a novel dual-template molecularly imprinted polymer (MIP)-coated stir bar was prepared and coupled with high-performance liquid chromatography (HPLC) for the analysis of environmental estrogens in complex samples. Dual-template MIP coating was homogeneous and porous with an average
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
Tadashi Toyama et al.
Applied and environmental microbiology, 76(20), 6733-6740 (2010-08-31)
We isolated three Sphingobium fuliginis strains from Phragmites australis rhizosphere sediment that were capable of utilizing 4-tert-butylphenol as a sole carbon and energy source. These strains are the first 4-tert-butylphenol-utilizing bacteria. The strain designated TIK-1 completely degraded 1.0 mM 4-tert-butylphenol
Yuka Ogata et al.
Biodegradation, 24(2), 191-202 (2012-07-11)
Although 4-tert-butylphenol (4-t-BP) is a serious aquatic pollutant, its biodegradation in aquatic environments has not been well documented. In this study, 4-t-BP was obviously and repeatedly removed from water from four different environments in the presence of Spirodela polyrrhiza, giant
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

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