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Sigma-Aldrich

2-Isopropylphenol

98%

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About This Item

Fórmula linear:
(CH3)2CHC6H4OH
Número CAS:
88-69-7
Peso molecular:
136.19
Beilstein:
1363322
Número CE:
201-852-8
Número MDL:
MFCD00002224
Código UNSPSC:
12352100
ID de substância PubChem:
24847907
NACRES:
NA.22

pressão de vapor

<0.05 mmHg ( 25 °C)

Ensaio

98%

índice de refração

n20/D 1.526 (lit.)

pb

212-213 °C (lit.)

pf

12-16 °C (lit.)

densidade

1.012 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CC(C)c1ccccc1O

InChI

1S/C9H12O/c1-7(2)8-5-3-4-6-9(8)10/h3-7,10H,1-2H3

chave InChI

CRBJBYGJVIBWIY-UHFFFAOYSA-N

Informações sobre genes

human ... GABRA1(2554)

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Descrição geral

2-Isopropylphenol is catabolized via a broad-spectrum meta cleavage pathway.

Aplicação

2-Isopropylphenol was used to study the ability of 2-isopropylphenol to activate estrogen receptor (ER), androgen receptor (AR), progesterone receptor (PR) and estrogen-related receptor (ERR).

Pictogramas

CorrosionExclamation mark
GHS05,GHS07

Palavra indicadora

Danger

Frases de perigo

H302,H314

Classificações de perigo

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

224.6 °F - closed cup

Ponto de fulgor (°C)

107 °C - closed cup

Equipamento de proteção individual

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

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Jian Li et al.
Toxicology in vitro : an international journal published in association with BIBRA, 24(1), 201-207 (2009-09-22)
Some phenols have been suspected to modulate the endocrine systems of wildlife and humans, but less is known about their interactions with different types of nuclear receptors. In this study, the ability of 2-tert-butylphenol, 2-isopropylphenol, 4-tert-octylphenol (4-t-OP), 2,4-dichlorophenol (2,4-DCP), 3,4-dichlorophenol
F Reichlin et al.
Applied and environmental microbiology, 60(12), 4587-4591 (1994-12-01)
Pseudomonas sp. strain HBP1 Prp grew on 2-isopropylphenol as the sole carbon and energy source with a maximal specific growth rate of 0.14 h-1 and transient accumulation of isobutyric acid. Oxygen uptake experiments with resting cells and enzyme assays with
Martin Barann et al.
Anesthesia and analgesia, 106(3), 846-857 (2008-02-23)
5-Hydroxytryptamine type 3 (5-HT3) receptors are excitatory ligand-gated ion channels which are involved in postoperative nausea and vomiting. They are depressed by the anesthetic propofol, which, in contrast, enhances the activity of inhibitory ligand-gated ion channels such as gamma-aminobutyric acid
Yongnian Ni et al.
Talanta, 76(3), 513-521 (2008-07-01)
The binding interaction of the pesticide Isoprocarb and its degradation product, sodium 2-isopropylphenate, with bovine serum albumin (BSA) was studied by spectrofluorimetry under simulated physiological conditions. Both Isoprocarb and sodium 2-isopropylphenate quenched the intrinsic fluorescence of BSA. This quenching proceeded
Kevin A Harvey et al.
Bioorganic & medicinal chemistry, 18(5), 1866-1874 (2010-02-16)
The present study describes the characterization and evaluation of novel anticancer conjugates, 2,6-diisopropylphenol-docosahexaenoate (PP-DHA), and its analogues including 2,4-diisopropylphenol-docosahexaenoate (DIPP-DHA), 2-isopropylphenol-docosahexaenoate (IPP-DHA), 2-cyclohexanephenol-docosahexaenoate (CHP-DHA) and phenol-docosahexaenoate (P-DHA) on breast cancer cell lines. Representative breast cancer cell lines, based on estrogen
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