4,4'-メチレンビス(2,6-ジ-tert-ブチルフェノール)(118-82-1)

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4,4'-メチレンビス(2,6-ジ-tert-ブチルフェノール) 製品概要
化学名:4,4'-メチレンビス(2,6-ジ-tert-ブチルフェノール)
英語化学名:4,4'-Methylenebis(2,6-di-tert-butylphenol)
别名:antioxidante702;Bimox M;bimoxm;Binox M;binoxm;binox-m;bis(4-Hydroxy-3,5-ditertbutyl)phenylmathane;Di(4-hydroxy-3,5-di-tert-butylphenyl)methane
CAS番号:118-82-1
分子式:C29H44O2
分子量:424.66
EINECS:204-279-1
カテゴリ情報:Antioxidant;Organics;Diphenylmethanes (for High-Performance Polymer Research);Functional Materials;Reagent for High-Performance Polymer Research;Bisphenol and Sulfonyldiphenol Monomers;Monomers;Polymer Science;Industrial/Fine Chemicals
Mol File:118-82-1.mol
4,4'-メチレンビス(2,6-ジ-tert-ブチルフェノール)
4,4'-メチレンビス(2,6-ジ-tert-ブチルフェノール) 物理性質
融点 155-159 °C(lit.)
沸点 289 °C40 mm Hg(lit.)
比重(密度) 0.99 g/cm3 (20℃)
蒸気圧0Pa at 25℃
屈折率 1.4875 (estimate)
闪点 289°C/40mm
貯蔵温度 Store below +30°C.
溶解性<0.0001g/l
酸解離定数(Pka)12.03±0.40(Predicted)
外見 solid
White
水溶解度 31.9ng/L at 20℃
BRN 1916919
安定性:Stable for 2 years from date of purchase as supplied. Solutions are not stable. Solutions must be made fresh and used within 1 working day.
InChIKeyMDWVSAYEQPLWMX-UHFFFAOYSA-N
LogP8.9 at 25℃
CAS データベース118-82-1(CAS DataBase Reference)
NISTの化学物質情報Phenol, 4,4'-methylenebis[2,6-bis(1,1-dimethylethyl)-(118-82-1)
EPAの化学物質情報Phenol, 4,4'-methylenebis[2,6-bis(1,1-dimethylethyl)- (118-82-1)
安全性情報
主な危険性 Xi
Rフレーズ 36/37/38-38-37-36
Sフレーズ 26-36
WGK Germany 1
RTECS 番号SL9650000
TSCA Yes
HSコード 29072990
毒性LD50 oral in rat: > 24gm/kg
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
4,4'-メチレンビス(2,6-ジ-tert-ブチルフェノール) Usage And Synthesis
外観白色~黄赤色~緑色粉末~結晶
説明bis-BHT (118-82-1) is a potent antioxidant. Cell permeable.
化学的特性light yellow crystalline
使用Antioxidant.
定義ChEBI: 4,4'-Methylenebis(2,6-di-tert-butylphenol) is a diarylmethane.
主な応用4,4'-Methylenebis(2,6-di-tert-butylphenol), also known as H2-4DBP, could be used as a ligand to react with sets of M(OR)x and MRx. The ligand possesses more flexibility than OBzP or catecholate derivatives, and the para-OH makes it of interest for controlled alcoholysis. This compound has several characteristics, including (i) the ortho position possesses the sterically hindering t-butyl group which will assist in minimizing oligomerization, (ii) the para linkage prevents chelation of the 4DBP ligand to the metal upon coordination, and (iii) may act as a valuable model for complexation behavior of the plastic precursor bisphenol-A [BPA; 4,4' -(propane-2,2-diyl)diphenol] that has become of recent concern[2].
燃焼性と爆発性Non flammable
参考文献1) Amorati et al. (2003), Antioxidant activity of 0-bisphenols: the role of intramolecular hydrogen bonding; J. Org. Chem. 68 5198.
[2] T. Boyle, Daniel T Yonemoto, L. Steele. “Synthesis and characterization of 4,4′-methylenebis (2,6-di-tert-butylphenol) derivatives of a series of metal alkoxides and alkyls.” Journal of Coordination Chemistry 65.1(2012): 487–505.
Tags:118-82-1