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Merck
CN

87307

Tetrahexylammonium iodide

≥99.0% (AT)

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About This Item

Linear Formula:
[CH3(CH2)5]4N(I)
CAS Number:
Molecular Weight:
481.58
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-382-4
Beilstein/REAXYS Number:
4164997
MDL number:
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InChI key

VRKHAMWCGMJAMI-UHFFFAOYSA-M

InChI

1S/C24H52N.HI/c1-5-9-13-17-21-25(22-18-14-10-6-2,23-19-15-11-7-3)24-20-16-12-8-4;/h5-24H2,1-4H3;1H/q+1;/p-1

SMILES string

[I-].CCCCCC[N+](CCCCCC)(CCCCCC)CCCCCC

assay

≥99.0% (AT)

form

powder

mp

99-101 °C

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

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

Regulatory Information

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T M W J Bandara et al.
Physical chemistry chemical physics : PCCP, 22(22), 12532-12543 (2020-05-27)
A series of highly efficient quasi-solid-state dye-sensitized solar cells (DSCs) is prepared by harnessing the binary cation effect and positive effects of the selected performance enhancers of gel-polymer electrolytes. The new electrolyte is composed of polyacrylonitrile polymer, tetra-hexylammonium iodide (Hex4NI)
Zeynep S Teksin et al.
Journal of controlled release : official journal of the Controlled Release Society, 116(1), 50-57 (2006-10-20)
Parallel Artificial Membrane Permeability Assay (PAMPA) is a method to screen drug candidates for membrane permeability. The objective was to characterize the transport of a model weak base, metoprolol, across a three lipid-component PAMPA system (denoted A-PAMPA, for anionic-PAMPA) and
The effects of tetrahexylammonium chloride on calcium mobilization from cerebellar microsomes.
L G Sayers et al.
Biochemical Society transactions, 21(2), 105S-105S (1993-05-01)
A M Lisi et al.
Journal of chromatography, 581(1), 57-63 (1992-10-02)
A simple and efficient procedure has been developed for the derivatization of diuretic agents in human urine by direct extractive alkylation and their detection by gas chromatography-mass spectrometry. The procedure is an improvement over previous extractive alkylation methods because of
N Surendran et al.
Journal of chromatography. B, Biomedical sciences and applications, 691(2), 305-312 (1997-04-11)
The objective of this research was to develop a rapid, sensitive and reliable method for the separation of phosphonodipeptide prodrugs and parent compounds to facilitate the evaluation of cell permeation using in vitro cell culture models. Separation was accomplished isocratically

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