推荐产品
蒸汽密度
>1 (vs air)
质量水平
方案
98%
表单
crystals
沸点
212-213 °C (lit.)
mp
59-61 °C (lit.)
SMILES字符串
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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一般描述
对 4-异丙基苯酚的声化学降解进行了研究 。
应用
乙烯基化合物的合成中使用了 4-异丙基苯酚 。
警示用语：
Danger
危险分类
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
储存分类代码
8B - Non-combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
230.0 °F - Pensky-Martens closed cup
闪点(°C)
110 °C - Pensky-Martens closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
危险化学品
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
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
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
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