Methadon

(+/-)-METHADONE Struktur
76-99-3
CAS-Nr.
76-99-3
Bezeichnung:
Methadon
Englisch Name:
(+/-)-METHADONE
Synonyma:
k174;Adanon;Amidone;Mecodin;Eptadone;Diaminon;Dolophin;Heptanon;Ketalgin;Methadon
CBNumber:
CB9707025
Summenformel:
C21H27NO
Molgewicht:
309.45
MOL-Datei:
76-99-3.mol

Methadon Eigenschaften

Schmelzpunkt:
78°
Siedepunkt:
449.71°C (rough estimate)
Dichte
1.0350 (rough estimate)
Brechungsindex
1.5614 (estimate)
Flammpunkt:
9℃
storage temp. 
−20°C
pka
pKa 8.25 (Uncertain)
EPA chemische Informationen
3-Heptanone, 6-(dimethylamino)-4,4-diphenyl- (76-99-3)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
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 76-99-3(Hazardous Substances Data)
Toxizität LD50 oral in rat: 86mg/kg
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H225 Flüssigkeit und Dampf leicht entzündbar. Entzündbare Flüssigkeiten Kategorie 2 Achtung GHS hazard pictogramssrc="/GHS02.jpg" width="20" height="20" /> P210,P233, P240, P241, P242, P243,P280, P303+ P361+P353, P370+P378,P403+P235, P501
H370 Schädigt die Organe. Spezifische Zielorgan-Toxizität (einmalige Exposition) Kategorie 1 Achtung GHS hazard pictogramssrc="/GHS08.jpg" width="20" height="20" /> P260, P264, P270, P307+P311, P321,P405, P501
Sicherheit
P210 Von Hitze, heißen Oberflächen, Funken, offenen Flammen und anderen Zündquellenarten fernhalten. Nicht rauchen.
P260 Dampf/Aerosol/Nebel nicht einatmen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P301+P310 BEI VERSCHLUCKEN: Sofort GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P311 GIFTINFORMATIONSZENTRUM/Arzt anrufen.

Methadon Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

Analgesic (narcotic).

Definition

ChEBI: A ketone that is heptan-3-one substituted by a dimethylamino group at position 6 and two phenyl groups at position 4.

Biologische Funktion

Methadone (Dolophine) has an analgesic profile and potency similar to that of morphine but a longer duration of action and better oral bioavailability.The kinetic properties of methadone and its derivative, LAAM, have been shown to be useful in the treatment of opioid addiction. Methadone is a useful analgesic drug for the treatment of moderate to severe pain. Unlike morphine, it is generally not used epidurally because of its long duration of action. It is also rarely or never used in PCA systems or in pregnant women during labor. The side effects and signs of overdose following methadone administration are similar to those observed with morphine. Overdose is treated with naloxone. Clearance of methadone is via the urine and bile as the cyclic Ndemethylated drug. The ability to N-demethylate the drug decreases in elderly patients, prolonging the action of methadone. In such patients, dosing intervals should be longer than in younger patients. In addition, the pH of the urine has a major effect on clearance of the drug. Alkalinization of the urine or renal insufficiency decreases excretion of the drug.
Drug interactions and precautions for the use of methadone are similar to those of morphine. In addition, rifampicin and hydantoins markedly increase the metabolism of methadone and can precipitate withdrawal from methadone. Conversely, the tricyclic antidepressants and certain benzodiazepines can inhibit metabolism of methadone, thereby increasing accumulation of the drug, prolonging its half-life, and intensifying its side effects. Continuous dosing with methadone may lead to drug accumulation and to an increased incidence of side effects; methadone is generally not used for PCA. In pregnant heroin-addicted women, substitution of methadone for heroin has been shown to be associated with fewer low-birth-weight newborns and fewer learning and cognition problems later in the life of the child.

Allgemeine Beschreibung

Methadone (Dolophine) is a synthetic opioid approved for analgesic therapy and for the maintenance and treatment of opioid addiction. Methadone is marketed as the racemate, although the opioid activity resides in the R-enantiomer (7–50 times more potent than the S-enantiomer). Methadone may only be dispensed for the treatment of opioid addiction by a program certified by the Federal Substance Abuse and Mental Health Services Administration.
Methadone is a μ-receptor agonist with complex and highly variable pharmacokinetic parameters. The major metabolic pathway of methadone metabolism is via Ndemethylation to an unstable product that spontaneously cyclizes to form the inactive 2-ethylidene-1,5-dimethyl-3,3- diphenylpyrrolidine (EDDP).

Pharmakologie

Methadone is a diphenylpropylamine. It has very good oral bioavailability (~85%) with an oral to parenteral ratio of 1:2. Its plasma half-life can be highly variable (3–50h, average 24h) but its duration of action is relatively short. With repeated dosing, problems with accumulation can occur because of this discrepancy between half-life and analgesic effect. Careful monitoring is therefore required when converting patients to long-term methadone. A lso, there is incomplete cross-tolerance with morphine. The racemic mixture in common use has agonist actions at the MOP receptor (mainly the laevo isomer) as well as antagonist activity at the NMDA receptor dextro isomer). Given the importance of this receptor in central sensitisation in a variety of pain states, there may be cases where methadone offers particular advantages over and above other opioids (e.g. neuropathic pain). Plasma concentrations of methadone can be reduced by carbamazepine, and its metabolism is accelerated by phenytoin.

Sicherheitsprofil

Poison by ingestion, intraperitoneal, intravenous, subcutaneous, and intraduodenal routes. Human systemic effects: coma, nausea or vomiting, respiratory changes, respiratory depression, somnolence. An experimental teratogen. Experimental reproductive effects. Caution: Abuse leads to habituation or addiction. When heated to decomposition it emits toxic fumes of NOx. See also METHADONE HYDROCHLORIDE.

Methadon Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

76-99-3(Methadon)Verwandte Suche:


  • 6-Dimethyamino-4,4-diphenyl-heptan-3-one
  • DL-METHADONE
  • methadona
  • Methadone M
  • methadone(l)
  • methadonum(latin)
  • methadose
  • Phenadone
  • Physeptone
  • Polamidon
  • Polamidone
  • Racemic methadone
  • 6-dimethylamino-4,4-diphenylheptan-3-one
  • Methadone {D.D.}
  • Methaquaione
  • 1,1-Diphenyl-1-[2-dimethylaminopropyl]-2-butanone
  • (RS)-Methadone
  • Eptadone
  • rac Methadone
  • Sedo-Rapide
  • Methadone (base and/or unspecified salts)
  • DL-6-Dimethylamino4,4-diphenyl-3-heptanone solution
  • DL-Methadone solution
  • (±)-Methdone
  • Methanol(test(±)-Methadone 1.0 mg/mL)
  • (+/-) METHADONE (5 AMPS/PKGE)
  • (±)-Methadone solution
  • 2-Dimethylamino-4,4-diphenyl-5-heptanone
  • 3-Heptanone, 6-(dimethylamino)-4,4-diphenyl-
  • 3-Heptanone, 6-(dimethylamino)-4,4-diphenyl-, (±
  • 6-(dimethylamino)-4,4-diphenyl-3-heptanon
  • 6-dimethylamino-4,4-diphenyl-3-heptanone
  • Adanon
  • Adanon hydrochloride
  • Algovetin
  • Amidone
  • Diaminon
  • Dolophin
  • Dolophine
  • Heptadone
  • Heptanon
  • heptanon(pharmaceutical)
  • k174
  • Ketalgin
  • Mecodin
  • Methadon
  • (+/-)-METHADONE
  • METHADONE
  • Methadone-13C6
  • (+/-)-METHADONE
  • Oxiconazole Impurity 13
  • 76-99-3
  • C21H27NO
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