InChI key
WMVJWKURWRGJCI-UHFFFAOYSA-N
InChI
1S/C16H26O/c1-7-15(3,4)12-9-10-14(17)13(11-12)16(5,6)8-2/h9-11,17H,7-8H2,1-6H3
SMILES string
CCC(C)(C)c1ccc(O)c(c1)C(C)(C)CC
assay
99%
bp
169-170 °C/22 mmHg (lit.)
mp
25 °C (lit.)
density
0.930 g/mL at 25 °C (lit.)
General description
The standard molar enthalpies of sublimation (or vaporization) of 2,4-di-tert-amylphenol have been evaluated. Preparation of 2,4-di-tert-amylphenol, via catalytic alkylation of phenol with trimethylethylene, is reported.
Application
2,4-Di-tert-amylphenol is a phenolic compound, used for the laccase induced coupling reactions. It may be used in the synthesis of Cu-phthalocyanine-C60.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Molecular association and monolayer formation of soluble phthalocyanine compounds.
Snow AW and Jarvis NL.
Journal of the Chemical Society, 106(17), 4706-4711 (1984)
Thermochemistry of phenols: quantification of the< i> ortho-,< i> para</i>-, and< i> meta</i>-interactions in tert-alkyl substituted phenols.
Verevkin SP.
The Journal of Chemical Thermodynamics, 31(5), 559-585 (1999)
Molecular association and monolayer formation of soluble phthalocyanine compounds.
Viktorova EA, et al.
Russian Chemical Bulletin, 9(8), 1402-1402 (1960)
Enzymatic synthesis of Tinuvin.
Schroeder M, et al.
Enzyme and Microbial Technology, 40(7), 1748-1752 (2007)
Yan-Hua Liu et al.
Ecotoxicology and environmental safety, 135, 90-97 (2016-10-11)
The occurrence and distribution of eight selected endocrine-disrupting chemicals were investigated in samples of surface water and suspended particulate matter (SPM) in Nanjing section of Yangtze River over a year (the flow period, the wet period and the dry period).
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