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506761

Supelco

4-tert-Butylphenol

PESTANAL®, analytical standard

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About This Item

Fórmula lineal:
(CH3)3CC6H4OH
Número de CAS:
98-54-4
Peso molecular:
150.22
Beilstein/REAXYS Number:
1817334
EC Number:
202-679-0
MDL number:
MFCD00002367
UNSPSC Code:
12000000
PubChem Substance ID:
24873390

grade

analytical standard

vapor pressure

1 mmHg ( 70 °C)

product line

PESTANAL®

CofA

current certificate can be downloaded

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

236-238 °C (lit.)

mp

96-101 °C (lit.)

density

0.908 g/mL at 25 °C (lit.)

application(s)

agriculture
cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

format

neat

storage temp.

2-30°C

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

This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

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

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Certificados de análisis (COA)

Lot/Batch Number
LRAD5374
LRAC8404
LRAC2277
LRAB8069
LRAB8045

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Rachael J Alessio et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 47(14), 2198-2204 (2012-09-01)
Octolig®, a polyethylenediimine ligand covalently attached to high-surface area silica gel, was used to study the removal of phenolic compounds from aqueous samples by column chromatography. Model phenolic compounds of Bisphenol A (BPA), 4-isopropylphenol and 4-(t-butyl) phenol, were selected for
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
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
Shingo Sato et al.
Chemical & pharmaceutical bulletin, 56(8), 1173-1176 (2008-08-02)
A method for the synthesis of calix[4 and 6]arenes with two or three alternately arranged phloroglucinols and p-tert-butylphenols was studied using "3+1" and "5+1" approaches, compared to a simple one-pot synthesis based on a "1+1" approach. By using Yb(OTf)3 as
Kai K Lie et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 150(2), 141-149 (2009-04-22)
The release of produced water (PW), a by-product of offshore oil production, has increased in Norwegian waters in recent years. Alkylphenols (AP), a major component of PW, have been shown to have endocrine disrupting effects on several fish species. In
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