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B99405

2-tert-Butylphenol

Name: 2-<I>tert</I>-Butylphenol
Brand: ALDRICH

99%

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About This Item

Linear Formula:

(CH₃)₃CC₆H₄OH

CAS Number:

88-18-6

Molecular Weight:

150.22

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24892164

EC Number:

201-807-2

Beilstein/REAXYS Number:

1907120

MDL number:

MFCD00002223

Assay:

99%

Form:

liquid

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Properties

vapor pressure

0.05 mmHg ( 20 °C)

Quality Level

100

assay

99%

form

liquid

refractive index

n20/D 1.523 (lit.)

bp

224 °C (lit.)

mp

−7 °C (lit.)

density

0.978 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)c1ccccc1O

InChI

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

InChI key

WJQOZHYUIDYNHM-UHFFFAOYSA-N

Gene Information

mouse ... Esr1(13982)

Description

pictograms

GHS06,GHS05,GHS09

signalword

Danger

hcodes

H302 + H332,H311,H314,H411

pcodes

P273 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 2

flash_point_f

215.6 °F - Pensky-Martens closed cup

flash_point_c

102 °C - Pensky-Martens closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品

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Effects of dietary and in vitro 2(3)-t-butyl-4-hydroxy-anisole and other phenols on hepatic enzyme activities in mice.

A D Rahimtula et al.

British journal of cancer, 45(6), 935-944 (1982-06-01)

Six phenols [2(3)-t-butyl-4-hydroxyanisole (BHA), 2-t-butylphenol, 4-methoxyphenol, 4-methylmercaptophenol, t-butylhydroquinone and 2,6-di-t-butylphenol] previously shown to be inhibitors of benzo(a)pyrene-induced neoplasia, were examined for their ability to induce in vivo changes in hepatic mono-oxygenase and detoxication enzyme activities, and to act as mono-oxygenase

Different pathways for 4-n-nonylphenol biodegradation by two Aspergillus strains derived from estuary sediment: Evidence from metabolites determination and key-gene identification.

Zonglin Yang et al.

Journal of hazardous materials, 359, 203-212 (2018-07-24)

Nonylphenols (NPs) are known as Endocrine Disputing Chemicals (ECDs) and Persistent Organic Pollutants (POPs) and have attracted continuous attention. Biodegradation is one of the effective ways for pollutant removal in aquatic, sedimentary and soil environments. In this study, two estuarine

Changing the substrate reactivity of 2-hydroxybiphenyl 3-monooxygenase from Pseudomonas azelaica HBP1 by directed evolution.

Andreas Meyer et al.

The Journal of biological chemistry, 277(7), 5575-5582 (2001-12-26)

The substrate reactivity of the flavoenzyme 2-hydroxybiphenyl 3-monooxygenase (EC, HbpA) was changed by directed evolution using error-prone PCR. In situ screening of mutant libraries resulted in the identification of proteins with increased activity towards 2-tert-butylphenol and guaiacol (2-methoxyphenol). One enzyme

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Global Trade Item Number

SKU	GTIN
B99405-500ML	04061833444054
B99405-50ML	04061833444061