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02799

Supelco

Tetramethylammonium sulfate

suitable for ion pair chromatography, LiChropur, ≥99.0% (T)

Synonym(s):

Bis(tetramethylammonium) sulfate

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About This Item

Linear Formula:
[(CH3)4N]2(SO4)
CAS Number:
Molecular Weight:
244.35
Beilstein:
3918039
EC Number:
MDL number:
UNSPSC Code:
41116105
PubChem Substance ID:
NACRES:
NB.21

description

cationic

Quality Level

Assay

≥99.0% (T)

form

powder

quality

LiChropur

technique(s)

ion pair chromatography: suitable

λ

10 % in H2O

UV absorption

λ: 210 nm Amax: ≤0.1
λ: 220 nm Amax: ≤0.04
λ: 230 nm Amax: ≤0.03
λ: 260 nm Amax: ≤0.02
λ: 500 nm Amax: ≤0.02

suitability

corresponds to standard for RP gradient test
corresponds to standard for filter test

SMILES string

C[N+](C)(C)C.C[N+](C)(C)C.[O-]S([O-])(=O)=O

InChI

1S/2C4H12N.H2O4S/c3*1-5(2,3)4/h2*1-4H3;(H2,1,2,3,4)/q2*+1;/p-2

InChI key

KJFVITRRNTVAPC-UHFFFAOYSA-L

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Application


  • Separation of Gd-humic complexes and Gd-based magnetic resonance imaging contrast agent in river water with QAE-Sephadex A-25 for the fractionation analysis.: This study highlights the application of Tetramethylammonium sulfate in the separation of gadolinium complexes from river water using QAE-Sephadex A-25. The research demonstrates the effectiveness of this approach in environmental analytical chemistry, providing insights into the behavior and fate of contrast agents in natural water systems (Matsumiya et al., 2014).

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Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

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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Mei Fang et al.
Nanotechnology, 23(14), 145601-145601 (2012-03-22)
Magnetite nanoparticles have been prepared by co-precipitation using a custom-designed jet mixer to achieve rapid mixing (RM) of reactants in a timescale of milliseconds. The quick and stable nucleation obtained allows control of the particle size and size distribution via
Man Xu et al.
Environmental science & technology, 47(1), 110-118 (2012-06-12)
Elucidating dissolution kinetics and mechanisms at carbonate mineral-water interfaces is essential to many environmental and geochemical processes, including geologic CO(2) sequestration in deep aquifers. In the present work, effects of background electrolytes on dolomite (CaMg(CO(3))(2)) reactivity were investigated by measuring
L Lemée et al.
Bioresource technology, 117, 234-241 (2012-05-24)
Lignocellulosic biomass was submitted to a biological pretreatment prior to a catalytic hydroliquefaction in order to produce biofuel. The biodegradation process was conducted over 3 months in a reactor under controlled conditions. During the biodegradation process the organic matter was
N Kodiah Beyeh et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(18), 5552-5557 (2012-04-11)
The non-covalent interactions of different upper-rim-substituted C(2)-resorcinarenes with tetramethylammonium salts were analyzed in the gas phase in an Electrospray Ionization Fourier-transform ion-cyclotron-resonance (ESI-FTICR) mass spectrometer and by (1)H NMR titrations. The order of binding strengths of the hosts towards the
Aleksandr Saghyan et al.
Journal of neuroscience methods, 205(1), 110-118 (2012-01-11)
Numerous brain structures are composed of distinct layers and such stratification has a profound effect on extracellular diffusion transport in these structures. We have derived a more general form of diffusion equation incorporating inhomogeneities in both the extracellular volume fraction

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