Tetraethylammoniumchlorid

Bezeichnung:Tetraethylammoniumchlorid

CAS-Nr56-34-8

Englisch Name:Tetraethylammonium Chloride

CBNumberCB4136114

SummenformelC8H20ClN

Molgewicht165.7

MOL-Datei56-34-8.mol

Synonyma

Tetraethylammoniumchlorid

Tetraethylammoniumchlorid physikalisch-chemischer Eigenschaften

Schmelzpunkt	39°C
Siedepunkt	273.32°C (rough estimate)
Dichte	1.08
Brechungsindex	1.5480 (estimate)
storage temp.	Inert atmosphere,Room Temperature
Löslichkeit	methanol: 0.1 g/mL, clear, colorless
Aggregatzustand	Crystalline Powder
Farbe	white to light yellow
PH	4.0 to 7.0(50g/L, 25℃)
Wasserlöslichkeit	Soluble in water, ethanol, chloroform, or acetone
maximale Wellenlänge (λmax)	λ: 260 nm Amax: 0.03 λ: 280 nm Amax: 0.03
Sensitive	Hygroscopic
Merck	14,9200
BRN	3563247
Stabilität	Stable. Incompatible with strong oxidizing agents. Protect from moisture.
InChIKey	YMBCJWGVCUEGHA-UHFFFAOYSA-M
CAS Datenbank	56-34-8(CAS DataBase Reference)
EPA chemische Informationen	Tetraethylammonium chloride (56-34-8)

Sicherheit

Kennzeichnung gefährlicher	Xn,Xi
R-Sätze:	22-36/37/38
S-Sätze:	26-36-37/39
WGK Germany	3
RTECS-Nr.	BS6125000
F	3-10
TSCA	Yes
HS Code	29239000
Toxizität	LD50 i.v. in dogs: 55.7-72.4 mg/kg (Keith, Jr.)

Gefahreninformationscode (GHS)

Tetraethylammonium Chloride Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R22:Gesundheitsschädlich beim Verschlucken.
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S37/39:Bei der Arbeit geeignete Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
Chemische Eigenschaften
white crystalline powder
Verwenden
Tetraethylammonium chloride (TEAC) has been used:
- used for inhibition of peroxynitrite induced relaxation in rat aorta rings
- as a pharmacological blocker of K⁺ current and Ca²⁺ induced K⁺ current in antennal lobe neurons
- for the induction of TEAC sensitive currents in cochlear inner hair cells digested with proteolytic enzymes and analyze its properties
Verwenden
Medicine (nerve-blocking agent).
Verwenden
Tetraethylammonium Chloride can be used as a source of tetraethylammonium ions for various pharmaceutical studies and has the ability to block K+ channels in various tissues. Tetraethylammonium Chloride can also block the transmission of nervous impulses across autonomic ganglions.
Definition
ChEBI: A quarternary ammonium chloride salt in which the cation has four ethyl substituents around the central nitrogen.
Allgemeine Beschreibung
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Biologische Aktivität
Non-selective K + channel blocker.
Biochem/physiol Actions
Tetraethylammonium chloride (TEAC) blocks K+ channels non-specifically. In rat aorta rings, tetraethylammonium inhibits relaxation induced by peroxynitrite. It blocks nicotinic acetylcholine neurotransmission by blocking the receptor-mediated K+ currents. TEAC can increase the contractility and mobility of colon and rectum and is a therapeutic option for Hirschsprung′s disease patients. TEAC reduces the inflammatory responses, improves cardiac, vascular and hemodynamic properties during early sepsis in animals. TEAC has cytotoxic and anti-proliferative potential and induces apoptosis in glioma cells by downregulating B-cell lymphoma-2 (Bcl-2) and upregulating Bcl-2 associated X (Bax).
in vitro
tetraethylammonium (tea) is a small ion that is thought to block open k channels by binding either to an internal or to an external site. for this reason, it has been used to probe the ion conduction pathway or pore of k channel mutants and a k channel chimera. tea blocks k+ channels at two sites, which define the inner and outer mouths of the channel pores [1].
in vivo
vasorelaxant effect of taurine can be diminished by tea in rat isolated arteries [2]
Lager
Room temperature (desiccate)
läuterung methode
Crystallise the chloride from EtOH by adding diethyl ether, from warm water by adding EtOH and diethyl ether, from dimethylacetamide or from CH2Cl2 by addition of diethyl ether. Dry it over P2O5 in vacuum for several days. It also crystallises from acetone/CH2Cl2/hexane (2:2:1) [Blau & Espenson J Am Chem Soc 108 1962 1986, White & Murray J Am Chem Soc 109 2576 1987]. [Beilstein 4 IV 332.]
Einzelnachweise
[1] taglialatela m, vandongen am, drewe ja, joho rh, brown am, kirsch ge. patterns of internal and external tetraethylammonium block in four homologous k+ channels. mol pharmacol. 1991 aug;40(2):299-307.
[2] niu lg, zhang ms, liu y, xue wx, liu db, zhang j, liang yq. vasorelaxant effect of taurine is diminished by tetraethylammonium in rat isolated arteries. eur j pharmacol. 2008 feb 2;580(1-2):169-74. epub 2007 oct 25.
[3] shea pa, dunklee pe, et al. preliminary clinical investigation of tetraethylammonium chloride with particular reference to disorders of the circulatory system. calif med. 1948 sep;69(3):193-6.

Tetraethylammonium Chloride Upstream-Materialien And Downstream Produkte

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