86862
Tetrabutylammonium chloride solution
suitable for ion pair chromatography, LiChropur™, concentrate, ampule
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C16H36ClN
CAS Number:
Molecular Weight:
277.92
UNSPSC Code:
12352200
NACRES:
NB.21
PubChem Substance ID:
EC Number:
214-195-7
Beilstein/REAXYS Number:
3571227
MDL number:
description
cationic
Quality Level
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
SMILES string
[Cl-].CCCC[N+](CCCC)(CCCC)CCCC
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
InChI key
NHGXDBSUJJNIRV-UHFFFAOYSA-M
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
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 36732-1G | 04061831827118 |
| CRM43557-100MG | 04061842646869 |
| 86862-6EA-KC | 04061833695166 |
| 86862-1AMP | 04061838095428 |