175404
4-异丙基苯酚
98%
别名:
对枯烯醇
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关于此项目
线性分子式:
(CH3)2CHC6H4OH
化学文摘社编号:
分子量:
136.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-798-8
Beilstein/REAXYS Number:
1363564
MDL number:
Assay:
98%
Form:
crystals
InChI key
YQUQWHNMBPIWGK-UHFFFAOYSA-N
InChI
1S/C9H12O/c1-7(2)8-3-5-9(10)6-4-8/h3-7,10H,1-2H3
SMILES string
CC(C)c1ccc(O)cc1
vapor density
>1 (vs air)
assay
98%
form
crystals
bp
212-213 °C (lit.)
mp
59-61 °C (lit.)
Quality Level
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General description
对 4-异丙基苯酚的声化学降解进行了研究 。
Application
乙烯基化合物的合成中使用了 4-异丙基苯酚 。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
存储类别
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
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
危险化学品
此项目有
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
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
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
Mahdi Chiha et al.
Ultrasonics sonochemistry, 17(5), 773-782 (2010-04-15)
Sonochemical degradation of phenol (Ph), 4-isopropylphenol (4-IPP) and Rhodamine B (RhB) in aqueous solutions was investigated for a large range of initial concentrations in order to analyze the reaction kinetics. The initial rates of substrate degradation and H(2)O(2) formation as
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
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