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线性分子式:
(CH3CH2CH2CH2)4N(I)
化学文摘社编号:
分子量:
369.37
UNSPSC Code:
23151817
NACRES:
NB.21
PubChem Substance ID:
EC Number:
206-220-5
Beilstein/REAXYS Number:
3916152
MDL number:
产品名称
四丁基碘化铵, suitable for ion pair chromatography, LiChropur™, ≥99.0%
InChI key
DPKBAXPHAYBPRL-UHFFFAOYSA-M
InChI
1S/C16H36N.HI/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H/q+1;/p-1
SMILES string
[I-].CCCC[N+](CCCC)(CCCC)CCCC
description
cationic
assay
≥99.0% (AT)
≥99.0%
form
crystals
quality
LiChropur™
technique(s)
ion pair chromatography: suitable
mp
141-143 °C (lit.)
144-148 °C
λ
10 % in acetonitrile
UV absorption
λ: 290 nm Amax: 0.1
λ: 300 nm Amax: 0.05
λ: 320 nm Amax: 0.02
λ: 500 nm Amax: 0.02
suitability
corresponds to standard for filter test
Quality Level
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Application
Tetrabutylammonium iodide may be used as a mobile phase additive in ion-pair high-performance liquid chromatography (IP-HPLC) assay of 4-aminopyridine in serum. Tetrabutylammonium iodide may also be used as a mobile phase additive in the analysis of tetracycline by reversed-phase IPC. The addition of tetrabutylammonium iodide regulates the retention of tetracyclines.
General description
Tetrabutylammonium iodide is an ion-pair chromatography (IPC) reagent suitable for anionic separation sorted by carbon chain length.
Legal Information
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Ion-pair high-performance liquid chromatographic assay of 4-aminopyridine in serum
Shinohara Y, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 230(2), 363-372 (1982)
Reversed-phase ion-pair liquid chromatography of tetracyclines
Eksborg S and Ekqvist B
Journal of Chromatography A, 209(2), 161-173 (1981)
Fabio Galeotti et al.
Journal of chromatography. A, 1284, 141-147 (2013-03-05)
In this study, by using tetrabutylammonium bisulfate as ion-pairing reagent, we were able to separate all the main heparin/heparan sulfate disaccharides generated by the action of heparinases along with the main Hep tetrasaccharide possessing a 3-O-sulfate group on the sulfoglucosamine
Erbo Shi et al.
Organic letters, 14(13), 3384-3387 (2012-06-27)
A metal-free C-H oxidation for the construction of allylic esters has been developed. The use of a commercially available and inexpensive catalyst and oxidant, and readily available starting materials, coupled with the operational simplicity of the reaction, renders the methodology
Morteza Moradi et al.
The Analyst, 137(15), 3549-3557 (2012-06-27)
Hollow fiber-based liquid phase microextraction (HF-LPME) using conventional solvents is limited by their relative instability and high volatility. The use of supramolecular solvents as a liquid membrane phase could overcome these inconveniences due to their negligible vapour pressure and high
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