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Merck

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:
Molecular Weight:
277.92
UNSPSC Code:
23151817
NACRES:
NB.21
PubChem Substance ID:
EC Number:
214-195-7
Beilstein/REAXYS Number:
3571227
MDL number:

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

Quality Level

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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
We are committed to bringing you Greener Alternative Products, which adhere to one or more of the 12 Principles of Green Chemistry. This product has been enhanced for catalytic efficiency. Find details here.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark

signalword

Warning

hcodes

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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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)
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
R Bryan Sears et al.
Journal of inorganic biochemistry, 121, 77-87 (2013-01-29)
The complex cis-[Ru(phpy)(phen)(CH3CN)2](+) (phpy=2-phenylpyridine, phen=1,10-phenanthroline) was investigated as a potential photodynamic therapy (PDT) agent. This complex presents desirable photochemical characteristics including a low energy absorption tail extending into the PDT window (600-850nm) and photoinduced exchange of the CH3CN ligands, generating
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

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