推荐产品
品質等級
化驗
≥97.0% (HPLC)
bp
285 °C (lit.)
mp
52-55 °C (lit.)
53-58 °C
溶解度
methanol: soluble 1 g/10 mL, clear, colorless to slightly yellow
SMILES 字串
CC(C)(C)c1ccc(O)c(O)c1
InChI
1S/C10H14O2/c1-10(2,3)7-4-5-8(11)9(12)6-7/h4-6,11-12H,1-3H3
InChI 密鑰
XESZUVZBAMCAEJ-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
一般說明
在酪氨酸酶的催化下，O2 存在下，4- 叔 -丁基邻苯二酚生成 4- 叔 -丁基- O -苯醌 。用循环伏安法和控制电位库仑法研究了 4--叔 -丁基邻苯二酚在 4-羟基香豆素存在下的电化学氧化。它通过阳极氧化进行电化学三聚反应，并利用循环伏安法和控制电位库仑法研究了三聚反应的机理 。
應用
- 儿茶酚和4-叔丁基儿茶酚的电化学氧化：探索儿茶酚和4-叔丁基儿茶酚的氧化反应，描述了电化学反应途径及在合成化学中的潜在应用(E Tammari, M Heravi, D Nematollahi, academia.edu)。
- 过氧化氢选择性氧化4-叔丁基苯酚：讨论钛硅材料在4-叔丁基儿茶酚选择性氧化反应中的催化性能，提高了选择性和产量(RR Talipova et al., Applied Petrochemical Research, 2016 - Springer)。
- 5-(叔丁基)-2,3-二羟基苯磺酸钡：研究4-叔丁基儿茶酚的磺化过程，用于开发新衍生物制备先进材料 (LG Rubicheva, DA Lukyanov - Molbank, 2022 - mdpi.com)。
- UV-AOP用于高效连续流去除4-叔丁基苯酚：比较去除水中污染物（如4-叔丁基儿茶酚）的不同高级氧化方法。说明环境应用(S Mergenbayeva, SG Poulopoulos - Processes, 2021 - mdpi.com)。
- 羟基自由基降解4-叔丁基苯酚：研究4-叔丁基儿茶酚的降解途径，深入了解环境影响和降解机制(YL Wu et al., China Environmental Science, 2016 - cabdirect.org)。
訊號詞
Danger
危險分類
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類（WGK）
WGK 3
閃點（°F）
235.4 °F - closed cup
閃點（°C）
113 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
其他客户在看
Electrochemical study of 3, 4-dihydroxybenzoic acid and 4-tert-butylcatechol in the presence of 4-hydroxycoumarin application to the electro-organic synthesis of coumestan derivatives.
Golabi SM and Nematollahi D.
Journal of Electroanalytical Chemistry, 430(1), 141-146 (1997)
Mechanistic study of electrochemical oxidation of 4-tert-butylcatechol: A facile electrochemical method for the synthesis of new trimer of 4-tert-butylcatechol.
Nematollahi D, et al.
Electrochimica Acta, 49(15), 2495-2502 (2004)
J N Rodriguez-López et al.
Analytical biochemistry, 202(2), 356-360 (1992-05-01)
A procedure for calibrating a Clark-type oxygen electrode is described. This method is based on the oxidation of 4-tert-butylcatechol (TBC) by O2 catalyzed by tyrosinase, to yield 4-tert-butyl-o-benzoquinone (TBCQ). This reaction consumes known amounts of oxygen in accordance with the
Keiko Minamoto et al.
Contact dermatitis, 46(6), 339-347 (2002-08-23)
Fibreglass-reinforced plastics (FRP) factory workers are at high risk of developing occupational dermatoses because of their exposure to many chemicals used in the manufacture of plastics as well as to glass fibre or dust. Patch tests were carried out on
T Kawashima et al.
The Journal of investigative dermatology, 82(1), 53-56 (1984-01-01)
4-Tertiary butyl catechol (TBC) causes depigmentation in humans and animals and stimulates formation of pheomelanosomes. In this study, we investigated the effects of noncytotoxic doses of TBC on glutathione S-transferase (GST) activity in the skin of Uscd strain mice and
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门