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506761

Supelco

4-tert-Butylphenol

PESTANAL®, analytical standard

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About This Item

Fórmula linear:
(CH3)3CC6H4OH
Número CAS:
98-54-4
Peso molecular:
150.22
Beilstein:
1817334
Número CE:
202-679-0
Número MDL:
MFCD00002367
Código UNSPSC:
12000000
ID de substância PubChem:
24873390

grau

analytical standard

pressão de vapor

1 mmHg ( 70 °C)

linha de produto

PESTANAL®

Certificado de análise (CofA)

current certificate can be downloaded

embalagem

ampule of 1000 mg

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

pb

236-238 °C (lit.)

pf

96-101 °C (lit.)

densidade

0.908 g/mL at 25 °C (lit.)

aplicação(ões)

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

formato

neat

temperatura de armazenamento

2-30°C

cadeia de caracteres SMILES

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

chave InChI

QHPQWRBYOIRBIT-UHFFFAOYSA-N

Informações sobre genes

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

Procurando produtos similares? Visita Guia de comparação de produtos

Descrição geral

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

Aplicação

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

Informações legais

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

Palavra indicadora

Danger

Frases de perigo

H315,H318,H361f,H410

Classificações de perigo

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

235.4 °F - closed cup

Ponto de fulgor (°C)

113 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
LRAD5374
LRAC8404
LRAC2277
LRAB8069
LRAB8045

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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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
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
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
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
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