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Sigma-Aldrich

4-Isopropylphenol

98%

Synonym(s):

p-Cumenol

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About This Item

Linear Formula:
(CH3)2CHC6H4OH
CAS Number:
99-89-8
Molecular Weight:
136.19
Beilstein:
1363564
EC Number:
202-798-8
MDL number:
MFCD00002372
UNSPSC Code:
12352100
PubChem Substance ID:
24850500
NACRES:
NA.22

vapor density

>1 (vs air)

Quality Level

100

Assay

98%

form

crystals

bp

212-213 °C (lit.)

mp

59-61 °C (lit.)

SMILES string

CC(C)c1ccc(O)cc1

InChI

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

InChI key

YQUQWHNMBPIWGK-UHFFFAOYSA-N

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General description

Sonochemical degradation of 4-Isopropylphenol has been studied.

Application

4-Isopropylphenol was used in the synthesis of vinyl compounds.

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302 + H312 + H332,H314

Hazard Classifications

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

Storage Class Code

8B - Non-combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

230.0 °F - Pensky-Martens closed cup

Flash Point(C)

110 °C - Pensky-Martens closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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David J Hopper et al.
Applied and environmental microbiology, 69(6), 3650-3652 (2003-06-06)
4-ethylphenol methylenehydroxylase from Pseudomonas putida JD1 acts by dehydrogenation of its substrate to give a quinone methide, which is then hydrated to an alcohol. It was shown to be active with a range of 4-alkylphenols as substrates. 4-n-propylphenol, 4-n-butylphenol, chavicol
Frédéric L P Gabriel et al.
Chemistry & biodiversity, 4(9), 2123-2137 (2007-09-25)
Sphingobium xenophagum Bayram is capable of metabolizing 4-alkoxyphenols and endocrine disruptive alpha-quaternary 4-nonylphenols by an ipso-substitution mechanism that involves ring hydroxylation at the site of the substituent. Here, we show that Bayram's ipso-hydroxylating activity was able to transform also bisphenol
D C Thompson et al.
Chemical research in toxicology, 8(1), 55-60 (1995-01-01)
The oxidative metabolism and toxicity of the para isomers of methylphenol (cresol), ethylphenol, and isopropylphenol were studied using male Sprague-Dawley rat liver microsomes and precision-cut liver slices. Reactive intermediates from each compound were trapped using radiolabeled glutathione and were detected
Ye Eun Park et al.
Nutrients, 12(1) (2020-01-23)
Probiotics can improve the intestinal environment by enhancing beneficial bacteria to potentially regulate lipid levels; however, the underlying mechanisms remain unclear. The aim of this study was to investigate the effect of Lactobacillus plantarum Q180 (LPQ180) on postprandial lipid metabolism
H Tamura et al.
Chemico-biological interactions, 104(1), 1-9 (1997-04-18)
Mouse nasal cytosols show high sulfotransferase (ST) activities toward phenolic aromatic odorants, but have little activities for most alcoholic aromatic odorants. Most ST activities toward the phenolic odorants preferred slightly acidic pH (6.4) and were sensitive to 2,6-dichloro-4-nitrophenol, a specific
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