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86903

Tetrabutylammonium iodide

suitable for ion pair chromatography, LiChropur™, ≥99.0%

Synonym(s):

TBAI

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About This Item

Linear Formula:
(CH3CH2CH2CH2)4N(I)
CAS Number:
311-28-4
Molecular Weight:
369.37
UNSPSC Code:
23151817
NACRES:
NB.21
PubChem Substance ID:
329769349
EC Number:
206-220-5
Beilstein/REAXYS Number:
3916152
MDL number:
MFCD00011636
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description

cationic

Quality Level

100

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

SMILES string

[I-].CCCC[N+](CCCC)(CCCC)CCCC

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

InChI key

DPKBAXPHAYBPRL-UHFFFAOYSA-M

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.

Other Notes

Discover LiChropur™ reagents ideal for HPLC or LC-MS analysis

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC3651
BCCB7747

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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
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Global Trade Item Number

SKUGTIN
86903-2.5G-F04061833347164
86903-10G-F04061838672827