557811
2,4-ジイソプロピルフェノール
98%
別名:
2,4-Bis(1-methylethyl)phenol, 2,4-Bis(propan-2-yl)phenol, 2,4-Di(propan-2-yl)phenol
ログインで組織・契約価格をご覧ください。
サイズを選択してください
この商品について
化学式:
[(CH3)2CH]2C6H3OH
CAS番号:
分子量:
178.27
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
220-906-1
MDL number:
Assay:
98%
InChI key
KEUMBYCOWGLRBQ-UHFFFAOYSA-N
InChI
1S/C12H18O/c1-8(2)10-5-6-12(13)11(7-10)9(3)4/h5-9,13H,1-4H3
SMILES string
CC(C)c1ccc(O)c(c1)C(C)C
assay
98%
refractive index
n20/D 1.5130 (lit.)
bp
79-80 °C (lit.)
density
0.948 g/mL at 25 °C (lit.)
Quality Level
関連するカテゴリー
General description
2,4-Diisopropylphenol, commonly known as 2,4-propofol, is an isomeric form of propofol. EC50 Microtox (5min, 25°C) assay value of 2,4-diisopropylphenol is 2x10-4mM. It is formed as one of the reaction products from the reaction between boron fluoride with isopropyl phenyl ether.
Application
2,4-Diisopropylphenol may be used in the preparation of N,N-bis(3,5-diisopropyl-2-hydroxybenyl)-N′,N′-dimethyl-1,2-diaminoethane.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
保管分類
10 - Combustible liquids
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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。
第4類:引火性液体 + 第三石油類 + 危険等級III + 非水溶性液体
fsl
557811-5G: + 557811-VAR: + 557811-1G: + 557811-BULK:
jan
T P Heil et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 24(4), 349-360 (1989-08-01)
EC50 Microtox (5 min, 25 degrees C) assay values for 2-isopropylphenol, 3-isopropylphenol, 4-isopropylphenol, 2,4-diisopropylphenol, 2,5-diisopropylphenol 2,6-diisopropylphenol, 3,5-diisopropylphenol, carvacrol, thymol, thiophenol, and thiocresol ranged from 2 x 10(-2) mM for thymol (least toxic) to 2 x 10(-4) mM for 2,4-diisopropylphenol and
Organic Reactions with Boron Fluoride. V. The Rearrangement of Isopropylphenol, o-, m-and p-Cresyl Ethers.
Sowa FJ, et al.
Journal of the American Chemical Society, 55(8), 3402-3407 (1933)
rac-Lactide polymerization using aluminum complexes bearing tetradentate phenoxy-amine ligands.
Tang Z and Gibson VC.
European Polymer Journal, 43(1), 150-155 (2007)
Shanker Karunanithi et al.
eNeuro, 7(1) (2020-02-06)
Propofol is the most common general anesthetic used for surgery in humans, yet its complete mechanism of action remains elusive. In addition to potentiating inhibitory synapses in the brain, propofol also impairs excitatory neurotransmission. We use electrophysiological recordings from individual
Tomoaki Urabe et al.
European journal of pharmacology, 884, 173303-173303 (2020-07-19)
Propofol, most frequently used as a general anesthetic due to its versatility and short-acting characteristics, is thought to exert its anesthetic actions via GABAA receptors; however, the precise mechanisms of its adverse action including angialgia remain unclear. We examined the
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。.
製品に関するお問い合わせはこちら（テクニカルサービス）