SMILES string
[OH-].CCCC[N+](CCCC)(CCCC)CCCC
InChI
1S/C16H36N.H2O/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H2/q+1;/p-1
InChI key
VDZOOKBUILJEDG-UHFFFAOYSA-M
grade
ACS reagent
form
liquid
concentration
1.0 M in H2O, 1.0 M±0.02 M (ACS specification)
impurities
≤0.2% tributylamine
color
APHA: ≤30
refractive index
n20/D 1.389
density
1 g/mL at 25 °C
anion traces
carbonate (CO32-): ≤0.1%, chloride (Cl-): ≤0.08%
cation traces
K: ≤2 ppm, Na: ≤2 ppm
Quality Level
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General description
Tetrabutylammonium hydroxide (TBAH) solution it is a strong organic base. It enables the dispersion of fatty acids in water at room temperature which allows the formation of emulsions and foams. TBAH is used as a titrant in the potentiometric titration of weak acids in non-aqueous media.
Application
相转移催化剂。
Tetrabutylammonium hydroxide solution may be used in the following processes:
- Synthesis of carbon doped TiO2 (titanium dioxide).
- Synthesis of C60 derivative-hydroxylated fullerene epoxide.
- As a hydrolysis controlling agent in the prearation of TiO2 sol.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
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Natural monocrystalline pyrite as a sensor in non-aqueous solution: Part I: Potentiometric titration of weak acids in, N,N-dimethylformamide, methylpyrrolidone and pyridine.
Mihajlovic LV, et al.
Talanta, 64(4), 879-886 (2004)
Daylight photocatalysis by carbon-modified titanium dioxide.
Sakthivel S and Kisch H.
Angewandte Chemie (International Edition in English), 42(40), 4908-4911 (2003)
Journal of the Chemical Society. Chemical Communications, 1045-1045 (1990)
Low temperature deposition of TiO2 thin films on polyvinyl alcohol fibers with photocatalytical and antibacterial activities.
Liuxue Z, et al.
Applied Surface Science, 254(6), 1771-1774 (2008)
Synthesis and characterization of hydroxylated fullerene epoxide-an intermediate for forming fullerol.
Li T, et al.
Journal of Central South University of Technology, 6(1), 35-36 (1999)
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