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Merck
CN

86852

Tetrabutylammonium chloride

greener alternative

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

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About This Item

Linear Formula:
[CH3(CH2)3]4NCl
CAS Number:
1112-67-0
Molecular Weight:
277.92
UNSPSC Code:
23151817
NACRES:
NB.21
PubChem Substance ID:
329769495
EC Number:
214-195-7
Beilstein/REAXYS Number:
3571227
MDL number:
MFCD00011635

Key Documents

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Product Name

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

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

assay

≥99.0% (AT)
≥99.0%

form

crystals

quality

LiChropur™

greener alternative product characteristics

Catalysis
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sustainability

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technique(s)

ion pair chromatography: suitable

λ

10 % in H2O

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
λ: 500 nm Amax: 0.02

suitability

corresponds to standard for filter test

greener alternative category

Aligned

Quality Level

100

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Application

TBACl has been used as ion-pairing reagent in the mobile phase during the quantification of nitrate and nitrite in water and food samples by normal phase ion-pair high performance liquid chromatography.

General description

Tetrabutylammonium chloride (TBACl) is a quaternary ammonium salt.g
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Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL5365
BCCL8481
BCCG9266
BCCF6895
BCCC8905

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Simultaneous determination of nitrite and nitrate by normal phase ion-pair liquid chromatography.
Butt SB, Riaz M, Iqbal MZ.
Talanta, 55(4), 789-797 (2001)
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
Shintaro Itagaki et al.
Chemical communications (Cambridge, England), 48(74), 9269-9271 (2012-08-10)
In the presence of Rh(2)(OAc)(4) (OAc = acetate) and TBA(2)WO(4) (TBA = tetra-n-butylammonium), the N-silylation of indole derivatives with hydrosilanes efficiently proceeded to give the corresponding N-silylated indoles in high yields. Pyrrole and carbazole were also N-silylated with the combined
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