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
Enzymatic synthesis of Tinuvin.
Schroeder M, et al.
Enzyme and Microbial Technology, 40(7), 1748-1752 (2007)
Molecular association and monolayer formation of soluble phthalocyanine compounds.
Viktorova EA, et al.
Russian Chemical Bulletin, 9(8), 1402-1402 (1960)
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)
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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