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Merck
CN

86862

Tetrabutylammonium chloride solution

suitable for ion pair chromatography, LiChropur™, concentrate, ampule

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About This Item

Empirical Formula (Hill Notation):
C16H36ClN
CAS Number:
1112-67-0
Molecular Weight:
277.92
UNSPSC Code:
12352200
NACRES:
NB.21
PubChem Substance ID:
329769499
EC Number:
214-195-7
Beilstein/REAXYS Number:
3571227
MDL number:
MFCD00011635

Key Documents

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Product Name

Tetrabutylammonium chloride solution, suitable for ion pair chromatography, LiChropur™, concentrate, ampule

InChI key

NHGXDBSUJJNIRV-UHFFFAOYSA-M

InChI

1S/C16H36N.ClH/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

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

description

cationic

form

solution

quality

LiChropur™
ampule

packaging

ampule of 25 mL

technique(s)

ion pair chromatography: suitable

λ

in concentrate

UV absorption

λ: 220 nm Amax: 0.05
λ: 230 nm Amax: 0.04
λ: 250 nm Amax: 0.03
λ: 260 nm Amax: 0.02

suitability

corresponds to standard for filter test

Quality Level

100

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General description

Concentrate for 6x1 L ready-to-use solution. Dilute contents of one ampule (~0.3 M) to 1 L with HPLC grade water to obtain a 0.005 M eluent solution.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Noelia Luque et al.
Journal of chromatography. A, 1248, 74-83 (2012-06-26)
The suitability of a mixed-mode sorbent made up of admicelles of sodium dodecyl sulphate (SDS) and tetrabutylammonium (TBA) to extract and preserve pesticides from river and underground water was assessed. Pesticides belonging to different structural groups (i.e. triazines, carbamates, phenylureas
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.
David J Posson et al.
Nature structural & molecular biology, 20(2), 159-166 (2012-12-25)
Understanding how ion channels open and close their pores is crucial for comprehending their physiological roles. We used intracellular quaternary ammonium blockers, electrophysiology and X-ray crystallography to locate the voltage-dependent gate in MthK potassium channels from Methanobacterium thermoautotrophicum. Blockers bind
Ya-Wen Chang et al.
Physical review letters, 108(24), 247802-247802 (2012-09-26)
The phase behavior of charged disk suspensions displays a strong dependence on ionic strengths, as the interplay between excluded volume and electrostatic interactions determines the formation of glasses, gels, and liquid crystal states. The various ions in natural soil or
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