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113042

Sigma-Aldrich

Tetraethylammonium chloride hydrate

Synonym(s):

TEA chloride

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About This Item

Linear Formula:
(C2H5)4N(Cl) · xH2O
CAS Number:
56-34-8
Molecular Weight:
165.70 (anhydrous basis)
Beilstein:
3563247
EC Number:
200-267-5
MDL number:
MFCD00149992
UNSPSC Code:
12161900
PubChem Substance ID:
57646912
NACRES:
NA.25

Assay

≥97.0% (titration by HClO<SUB>4</SUB>)

mol wt

165.70 g/mol (anhydrous basis)

technique(s)

protein purification: suitable

SMILES string

[Cl-].[H]O[H].CC[N+](CC)(CC)CC

InChI

1S/C8H20N.ClH.H2O/c1-5-9(6-2,7-3)8-4;;/h5-8H2,1-4H3;1H;1H2/q+1;;/p-1

InChI key

CALLTGJPWMIDPC-UHFFFAOYSA-M

Application

Phase-transfer catalyst employed in polymerization reactions. Electrolyte used in membrane transport studies.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

201.2 °F - closed cup

Flash Point(C)

94 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Makromol. Chem., Rapid Commun., 14, 173-173 (1993)
H Tatsuta et al.
The Journal of general physiology, 103(3), 429-446 (1994-03-01)
Patch-clamp studies were carried out in villus enterocytes isolated from the guinea pig proximal small intestine. In the whole-cell mode, outward K+ currents were found to be activated by depolarizing command pulses to -45 mV. The activation followed fourth order
Coll. Polymer Sci., 272, 971-971 (1994)
Myung-Woo Byun
Journal of medicinal food, 15(11), 1032-1037 (2012-10-13)
Polyphenol-rich foods, such as fruits and vegetables, are protective against cardiovascular diseases, but the mechanisms of the beneficial effects are still unknown. The goal of this research was to clarify actions of procyanidin trimer (C1) in rat aortic endothelial cells
Jayabalan Nirmal et al.
Current eye research, 37(12), 1127-1135 (2012-08-25)
To evaluate the functional role of organic cation transporters (OCT) and ocular tissue distribution of intravitreally injected OCT substrate tetraethylammonium (TEA) in presence of OCT blocker (quinidine). New Zealand albino rabbits of either sex were used. Intravitreal quinidine pretreatment was
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