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Dibutylammonium acetate solution

0.5 M in H2O, LiChropur, suitable for ion pair chromatography

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Synonym(s):
Dibutylamine acetate Concentrate
Linear Formula:
(CH3CH2CH2CH2)2NH · CH3COOH
CAS Number:
Molecular Weight:
189.30
MDL number:
PubChem Substance ID:
NACRES:
NB.21

form

solution

Quality Level

quality

LiChropur

packaging

pkg of 25 ML Volume containing 10 ML of product

concentration

0.5 M in H2O

technique(s)

LC/MS: suitable
ion pair chromatography: suitable

refractive index

n20/D 1.348

SMILES string

CC(O)=O.CCCCNCCCC

InChI

1S/C8H19N.C2H4O2/c1-3-5-7-9-8-6-4-2;1-2(3)4/h9H,3-8H2,1-2H3;1H3,(H,3,4)

InChI key

MQFIKAWTCOXAAY-UHFFFAOYSA-N

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General description

Dibutylammonium acetate is an ion-pairing agent with quaternary ammonium ions. It generally helps in ionization of carbohydrate fragments providing a volatile solvent for the mass spectrometric technique.

Application

It has been used as buffer in mobile phase for separation and quantifying intracellular nucleotides from different microorganisms using ion pair reversed phase liquid chromatography electrospray ionization isotope dilution tandem mass spectrometry (IP–LC–ESI–ID–MS/MS) method.

Packaging

Clear borosilicate glass, high hydrolytic resistance (Type I)
concentrate in ampules for 6x1 l 0.005 M ready-to-use solution

Recommended products

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Simultaneous quantification of free nucleotides in complex biological samples using ion pair reversed phase liquid chromatography isotope dilution tandem mass spectrometry.
Seifar, Reza M., et al.
Analytical Biochemistry, 388.2, 213-219 (2009)
Valentina Izzo et al.
Cell cycle (Georgetown, Tex.), 16(3), 271-279 (2017-01-07)
Phase II clinical trials indicate that the combination of cysteamine plus epigallocatechin gallate (EGCG) is effective against cystic fibrosis in patients bearing the most frequent etiological mutation (CFTRΔF508). Here, we investigated the interaction between both agents on cultured respiratory epithelia
Christian D Laourdakis et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 967, 127-133 (2014-08-05)
Targeted metabolite profiling has aided in the understanding of a variety of biological processes in the malaria parasite as well as in drug discovery. A fast and sensitive analytical method, based on ion-pairing reversed phase ultra-high performance liquid chromatography tandem

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