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この商品について
化学式:
(CH3)2CHC6H4OH
CAS番号:
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
製品名
4-イソプロピルフェノール, 98%
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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関連するカテゴリー
Application
4-イソプロピルフェノールは、ビニル化合物の合成で使用されました。
General description
4-イソプロピルフェノールの音響化学分解が調べられています。
保管分類
8B - Non-combustible corrosive hazardous materials
wgk
WGK 3
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
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
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
175404-1KG: + 175404-VAR: + 175404-100G: + 175404-BULK: + 175404-250G: + 175404-5G:
jan
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
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
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
Shogo Kumagai et al.
Scientific reports, 8(1), 13994-13994 (2018-09-20)
The pyrolysis of bisphenol A (BPA), an essential process ingredient used in industry and many everyday life products, helps produce low-industrial-demand chemicals such as isopropenyl- and isopropyl-phenols (IPP and iPrP). In this study, tandem micro-reactor gas chromatography/mass spectrometry combined with
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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