86903
四丁基碘化铵
suitable for ion pair chromatography, LiChropur™, ≥99.0%
别名:
TBAI
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关于此项目
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:
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
Quality Level
mp
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
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General description
Tetrabutylammonium iodide is an ion-pair chromatography (IPC) reagent suitable for anionic separation sorted by carbon chain length.
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.
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
Reversed-phase ion-pair liquid chromatography of tetracyclines
Eksborg S and Ekqvist B
Journal of Chromatography A, 209(2), 161-173 (1981)
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)
Chao Zhong et al.
Carbohydrate polymers, 94(1), 38-45 (2013-04-03)
In this article, a novel and high efficient solvent, tetra-n-Butylammonium Hydroxide (TBAH), was used for dissolution and isolation of straw cellulose from wheat straw. The composition analysis with gas chromatography (GC) and the spectroscopic characterization analysis conducted by X-Ray diffraction
Shohei Sakashita et al.
Organic letters, 15(17), 4308-4311 (2013-08-21)
Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of tetrabutylammonium 2-pyridyltriolborate salts with various aryl (heteroaryl) chlorides can produce the corresponding desired coupling products with good to excellent yields. These tetrabutylammonium salts are more reactive than the corresponding lithium salts. The coupling reactions with
Kosei Sugahara et al.
Chemical communications (Cambridge, England), 48(67), 8422-8424 (2012-07-14)
A tetra-n-butylammonium (TBA) salt of a γ-Keggin -6-charged germanodecatungstate, [γ-H(2)GeW(10)O(36)](6-) (I), could act as an efficient homogeneous catalyst for Knoevenagel condensation of active methylene compounds with carbonyl compounds.
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