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W346101

Sigma-Aldrich

2-Isopropylphenol

≥98%, FG

Sinónimos:

2-propan-2-ylphenol, O-cumenol, Prodox 131

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About This Item

Fórmula lineal:
(CH3)2CHC6H4OH
Número de CAS:
88-69-7
Peso molecular:
136.19
FEMA Number:
3461
Beilstein/REAXYS Number:
1363322
EC Number:
201-852-8
Council of Europe no.:
11234
MDL number:
MFCD00002224
UNSPSC Code:
12164502
PubChem Substance ID:
24901714
Flavis number:
4.044
NACRES:
NA.21

biological source

synthetic

grade

FG
Fragrance grade
Halal

agency

follows IFRA guidelines
meets purity specifications of JECFA

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 872/2012
FDA

vapor pressure

<0.05 mmHg ( 25 °C)

assay

≥98%

refractive index

n20/D 1.526 (lit.)

bp

212-213 °C (lit.)

mp

12-16 °C (lit.)

density

1.012 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

organoleptic

medicinal

SMILES string

CC(C)c1ccccc1O

InChI

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

InChI key

CRBJBYGJVIBWIY-UHFFFAOYSA-N

Gene Information

human ... GABRA1(2554)

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Categorías relacionadas

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H302,H314

Hazard Classifications

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

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

224.6 °F - closed cup

flash_point_c

107 °C - closed cup

ppe

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

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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
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
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
Andrzej L Dawidowicz et al.
Journal of food science and technology, 52(7), 4523-4529 (2015-07-04)
The presented paper shows the influence of temperature increase in the range typically used during antioxidant measurements (15-35 °C) on the estimation of antioxidant properties of phenolic compounds (caffeic acid, ferulic acid, gallic acid, trolox, butylhydroxyanisole, butylhydroxytoluene and 2,6-diisopropylphenol) in associating
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