Sufentanil

Bezeichnung:Sufentanil

CAS-Nr56030-54-7

Englisch Name:Sufentanil

CBNumberCB51105211

SummenformelC22H30N2O2S

Molgewicht386.55

MOL-Datei56030-54-7.mol

Sufentanil physikalisch-chemischer Eigenschaften

Schmelzpunkt	103-104℃
Siedepunkt	493.1±40.0 °C(Predicted)
Dichte	1.20 g/cm³
Flammpunkt	9℃
storage temp.	2-8°C
Löslichkeit	Practically insoluble in water, freely soluble in ethanol (96 per cent) and in methanol.
Aggregatzustand	A neat solid
pka	7.89±0.20(Predicted)
Wasserlöslichkeit	76mg/L(25 ºC)

Sicherheit

Kennzeichnung gefährlicher	F,T
R-Sätze:	11-23/24/25-39/23/24/25
S-Sätze:	7-16-36/37-45
RIDADR	UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany	1
Giftige Stoffe Daten	56030-54-7(Hazardous Substances Data)
Toxizität	LD50 i.v. in mice: 18.7 mg/kg (Van Bever)

Gefahreninformationscode (GHS)

Sufentanil Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung
Sufentanil is a narcotic analgesic with a greater potency and therapeutic ratio than its structural relative fentanyl. It appears to produce fewer cardiac effects and less respiratory depression than fentanyl, and thus is especially useful as an analgesic/anesthetic in open heart surgery.
Beschreibung
Sufentanil (Item No. 15917) is an analytical reference material categorized as an opioid. Sufentanil is regulated as a Schedule II compound in the United States. This product is intended for research and forensic applications.
Chemische Eigenschaften
White or almost white powder.
Originator
Jaassen (Belgium)
Verwenden
Opioid receptor agonist; analgesic.
Definition
ChEBI: An anilide resulting from the formal condensation of the aryl amino group of 4-(methoxymethyl)-N-phenyl-1-[2-(2-thienyl)ethyl]piperidin-4-amine with propanoic acid.
Manufacturing Process
A mixture of 4.1 parts of N-[4-(methoxymethyl)-4-piperidinyl]-Nphenylpropanamide, 5.3 parts of sodium carbonate and 120 parts of 4- methyl-2-pentanone is stirred and refluxed with water-separator. Then there are added 4.1 parts of 2-thiopheneethanol methanesulfonate ester and stirring at reflux is continued for 18 hours. The reaction mixture is cooled, washed twice with water and evaporated. The oily residue is purified by columnchromatography over silica gel, using a mixture of trichloromethane and 5% of methanol as eluent. The first fraction is collected and the eluent is evaporated. The oily residue is converted into the hydrochloride salt in 2,2'- oxybispropane. The free base is liberated again in the conventional manner. After extraction with 2,2'-oxybispropane, the latter is dried, filtered and evaporated. The oily residue solidifies on triturating in petroleum-ether. The solid product is filtered off and crystallized from petroleum-ether at -20°C, yielding, after drying, N-[4-(methoxymethyl)-1-[2-(2-thienyl)ethyl]-4- piperidinyl]-N-phenylpropanamide; melting point 98.6°C.
Trademarks
SUFENTA
Therapeutic Function
Analgesic

Sufentanil Upstream-Materialien And Downstream Produkte

56030-54-7, Sufentanil Verwandte Suche:

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