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Merck

506761

Supelco

4-叔丁基苯酚

PESTANAL®, analytical standard

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About This Item

线性分子式:
(CH3)3CC6H4OH
CAS号:
分子量:
150.22
Beilstein:
1817334
EC號碼:
MDL號碼:
分類程式碼代碼:
12000000
PubChem物質ID:

等級

analytical standard

蒸汽壓力

1 mmHg ( 70 °C)

產品線

PESTANAL®

CofA

current certificate can be downloaded

包裝

ampule of 1000 mg

技術

HPLC: suitable
gas chromatography (GC): suitable

bp

236-238 °C (lit.)

mp

96-101 °C (lit.)

密度

0.908 g/mL at 25 °C (lit.)

應用

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

格式

neat

儲存溫度

2-30°C

SMILES 字串

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 密鑰

QHPQWRBYOIRBIT-UHFFFAOYSA-N

基因資訊

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

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一般說明

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

應用

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

法律資訊

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

訊號詞

Danger

危險分類

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

235.4 °F - closed cup

閃點(°C)

113 °C - closed cup

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

Lot/Batch Number

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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
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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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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
J Pablo Lamas et al.
Analytical and bioanalytical chemistry, 394(8), 2231-2239 (2009-07-07)
A method for the determination of dimethyl fumarate (DMF), benzothiazole (BT) and tert-butylphenol (TBP) in desiccant and antimould agents employed for protecting consumer products from humidity and mould has been developed. The method is based on ultrasound-assisted extraction (UAE) followed
Pierre Etienne Chabrier et al.
CNS drug reviews, 13(3), 317-332 (2007-09-27)
BN82451 belongs to a new family of small molecules designated as multitargeting or hybrid molecules. BN82451 is orally active, has good central nervous system penetration, and elicits potent neuronal protection and antiinflammatory properties. Neuronal protection is due to Na+ channel

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