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235954

Sigma-Aldrich

Tetrapropylammonium iodide

≥98%

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Linear Formula:
(CH3CH2CH2)4N(I)
CAS Number:
Molecular Weight:
313.26
Beilstein/REAXYS Number:
3567386
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥98%

form

solid

mp

280-285 °C (dec.) (lit.)

SMILES string

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

InChI

1S/C12H28N.HI/c1-5-9-13(10-6-2,11-7-3)12-8-4;/h5-12H2,1-4H3;1H/q+1;/p-1

InChI key

GKXDJYKZFZVASJ-UHFFFAOYSA-M

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1 of 4

This Item
235938140775438243
vibrant-m

235954

Tetrapropylammonium iodide

vibrant-m

235938

Tetraethylammonium iodide

vibrant-m

140775

Tetrabutylammonium iodide

vibrant-m

438243

Tetrapropylammonium chloride

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

assay

≥98%

assay

98%

assay

98%

assay

98%

mp

280-285 °C (dec.) (lit.)

mp

>300 °C (lit.)

mp

141-143 °C (lit.)

mp

240-242 °C (lit.)

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Alexey A Sysoev et al.
European journal of mass spectrometry (Chichester, England), 22(6), 289-296 (2016-12-03)
An ion mobility time-of-flight mass spectrometry (IM-TOFMS)-based method has been preliminarily investigated for the identification of triphenylmethane ballpoint pen dyes on paper. The dyes were sampled from one-year-old ballpoint pen ink entries. The entries were written on paper documents stored
Vidhya Selvanathan et al.
Polymers, 12(3) (2020-03-04)
This work is a pioneer attempt to fabricate quasi-solid dye-sensitized solar cell (QSDDSC) based on organosoluble starch derivative. Rheological characterizations of the PhSt-HEC blend based gels exhibited viscoelastic properties favorable for electrolyte fabrication. From amplitude sweep and tack test analyses
Hui Wang et al.
Physical chemistry chemical physics : PCCP, 17(32), 20636-20646 (2015-07-24)
The (13)C NMR chemical shift moving upfield indicates the main model of π-holeX(-) bond between cyanuric chloride/1,3,5-triazine (3ClN/3N), which possess both the π-hole and σ-hole, and X(-). (13)C NMR and UV absorption titration in acetonitrile confirmed that the bonding abilities

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