Tetraethylammonium iodide, 98+%
Tetraethylammonium iodide, 98+%
Tetraethylammonium iodide, 98+%
Thermo Scientific Chemicals

Tetraethylammonium iodide, 98+%

CAS: 68-05-3 | C8H20IN | 257.16 g/mol
数量:
50 g
250 g
1000 g
製品番号(カタログ番号) A11783.18
または、製品番号A11783-18
価格(JPY)
-
数量:
50 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS68-05-3
IUPAC Nametetraethylazanium iodide
Molecular FormulaC8H20IN
InChI KeyUQFSVBXCNGCBBW-UHFFFAOYSA-M
SMILES[I-].CC[N+](CC)(CC)CC
さらに表示
Appearance (Color)White
FormCrystalline powder or crystals
Assay (Titration ex Iodide)≥98.0 to ≤102.0% (non-U.S. specification)
Assay from Suppliers CofA≥98.0% (U.S specification)
CommentSpecification differs for U.S. and non-U.S. material where indicated
It has been used as the source of tetraethylammonium ions in pharmacological and physiological studies, but is also used in organic chemical synthesis.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It has been used as the source of tetraethylammonium ions in pharmacological and physiological studies, but is also used in organic chemical synthesis.

Solubility
Soluble in water almost transparency.

Notes
Light Sensitive and Hygroscopic. Store in dark and away from water/moisture. Keep container tightly closed in a dry and well-ventilated place. Store under dry inert gas.
RUO – Research Use Only

General References:

  1. Samuel J Goodchild; Hongjian Xu; Zeineb Es-Salah-Lamoureux; Christopher A Ahern; David Fedida. Basis for allosteric open-state stabilization of voltage-gated potassium channels by intracellular cations. Journal of General Physiology, 2012, 140 (5), 495-511.
  2. Ling Xiao et. al. Unique cardiac Purkinje fiber transient outward current β-subunit composition: a potential molecular link to idiopathic ventricular fibrillation. Circulation Research, 2013, 112 (10), 1310-1322.
  3. Reagent for conversion of ɑß-enones in TFA to ß-iodo ketones in high yield: Tetrahedron, 39, 1529 (1983).