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Merck

52371

Hexadecyltrimethylammonium bisulfate

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

Synonym(s):

Hexadecyltrimethylammonium hydrogen sulfate

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About This Item

Linear Formula:
CH3(CH2)15N(HSO4)(CH3)3
CAS Number:
Molecular Weight:
381.61
UNSPSC Code:
23151817
NACRES:
NB.21
PubChem Substance ID:
EC Number:
269-286-4
Beilstein/REAXYS Number:
8398798
MDL number:
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description

cationic

Quality Level

assay

≥99.0% (T)

form

solid

quality

LiChropur

technique(s)

ion pair chromatography: suitable

λ

10 % in H2O

UV absorption

λ: 210 nm Amax: 0.15, λ: 220 nm Amax: 0.10, λ: 260 nm Amax: 0.05, λ: 310 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

OS([O-])(=O)=O.CCCCCCCCCCCCCCCC[N+](C)(C)C

InChI

1S/C19H42N.H2O4S/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(2,3)4;1-5(2,3)4/h5-19H2,1-4H3;(H2,1,2,3,4)/q+1;/p-1

InChI key

UCRJJNVFJGKYQT-UHFFFAOYSA-M

General description

Hexadecyltrimethylammonium bisulfate is an ion pair reagent suitable for anionic separation sorted by carbon chain length.

Application

Hexadecyltrimethylammonium bisulfate may be used as an electrolyte modifier in studying the effect of alkyltrimethylammonium ions on corrosion and electrochemical behavior of Pb-Ca-Sn alloy.

Other Notes

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Effect of Alkyltrimethylammonium Ions on Corrosion and Electrochemical Behavior of Pb-Ca-Sn Alloy
Kopczynski K, et al.
International Journal of Electrochemical Science, 13, 11058-11073 (2018)
Amit Kumar Mandal et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 14(4), 788-796 (2012-11-13)
Femtosecond upconversion, single-molecule fluorescence resonance energy transfer (sm-FRET) and fluorescence correlation spectroscopy (FCS) are applied to study the competition between excited-state proton transfer (ESPT) and FRET [to rhodamine 6G (R6G)] of 8-hydroxypyranine-1,3,6-trisulfonate (HPTS) in cetyltrimethylammonium chloride (CTAC) micelles. Pyranine exhibits
Ruggero Angelico et al.
Physical chemistry chemical physics : PCCP, 15(2), 586-595 (2012-11-28)
The aim of the present study was to provide experimental evidence that base pairing, commonly occurring between nucleic bases in more complex supramolecular arrangements, may affect the reaction pathways associated with the alkylation of bases themselves. In pursuit of this