MEPHOBARBITAL

MEPHOBARBITAL Struktur
115-38-8
CAS-Nr.
115-38-8
Englisch Name:
MEPHOBARBITAL
Synonyma:
Metyna;Mebaral;Meberal;Mephytal;Morbusan;Phemiton;Prominal;Enfenemal;Menta-bal;Phemetone
CBNumber:
CB2207809
Summenformel:
C13H14N2O3
Molgewicht:
246.26
MOL-Datei:
115-38-8.mol

MEPHOBARBITAL Eigenschaften

Schmelzpunkt:
1760C
Siedepunkt:
389.26°C (rough estimate)
Dichte
1.1855 (rough estimate)
Brechungsindex
1.6450 (estimate)
Flammpunkt:
11 °C
storage temp. 
Controlled Substance, -20°C Freezer
Löslichkeit
Practically insoluble in water, very slightly soluble in ethanol (96 per cent).
pka
7.99±0.10(Predicted)
Aggregatzustand
Solid
Farbe
White to Off-White
Wasserlöslichkeit
0.15g/L(20 ºC)
CAS Datenbank
115-38-8
EPA chemische Informationen
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-1-methyl-5-phenyl- (115-38-8)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xn,T,F
R-Sätze: 22-39/23/24/25-23/24/25-11
S-Sätze: 36/37/39-45-36/37-16-7
RIDADR  3249
HazardClass  6.1(b)
PackingGroup  III
HS Code  2933530000
Giftige Stoffe Daten 115-38-8(Hazardous Substances Data)
Toxizität cat,LD50,oral,230mg/kg (230mg/kg),Drugs in Japan Vol. 6, Pg. 851, 1982.
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 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 P260, P264, P270, P307+P311, P321,P405, P501
Sicherheit
P210 Von Hitze, heißen Oberflächen, Funken, offenen Flammen und anderen Zündquellenarten fernhalten. Nicht rauchen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

MEPHOBARBITAL Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften

White Crystalline Solid

Verwenden

Controlled substance (depressant). Anticonvulsant; sedative; hypnotic

Definition

ChEBI: A member of the class of barbiturates, the structure of which is that of barbituric acid substituted at N-1 by a methyl group and at C-5 by ethyl and phenyl groups.

Allgemeine Beschreibung

Mephobarbital, 3-methyl-5-ethyl-5-phenylbarbituric acid (metharbital), is metabolicallyN-demethylated to phenobarbital, which many consider toaccount for almost all of the activity. Its principal use is asan anticonvulsant.

Clinical Use

Mephobarbital is a barbiturate-derivative AED with a pKa of 7.7 (log P = 1.84 at pH 7.4). Approximately 50% of an oral dose of mephobarbital is absorbed from the gastrointestinal tract. The plasma concentrations required for its therapeutic effects are unknown. The principal route of mephobarbital metabolism is N-demethylation by the liver to form phenobarbital, which may be excreted in the urine unchanged and as its p-hydroxy metabolite and glucuronide or sulfate conjugates. Conversion to the 4-hydroxy metabolite is stereoselective, being catalyzed by either CYP2C19 (R-enantiomer) or CYP2B6 (S-enantiomer); individuals who are CYP2C19 poor metabolizers show decreased clearance. Approximately 75% of a single oral dose of mephobarbital is converted to phenobarbital. It has not been determined whether mephobarbital contributes to the antiseizure effect or whether it results from its active metabolite, phenobarbital. Similarly, it is unclear whether mephobarbital, like phenobarbital, is a potent inducer of the enzymes involved in the metabolism of other drugs, but because the drug is chemically and pharmacologically similar to phenobarbital and is metabolized to phenobarbital, this possibility is likely.
Mephobarbital is less commonly used in the treatment of generalized and partial seizures. Like phenobarbital, it is classified as a long-acting barbiturate. No evidence exists that it is more effective than phenobarbital in equivalent doses; however, it may be less sedating in children.

Sicherheitsprofil

Poison by ingestion and intraperitoneal routes. A human teratogen by an unspecified route with developmental abnormalities of the cardovascular (circulatory) system. When heated to decomposition it emits toxic NOx. See also BARBITURATES.

MEPHOBARBITAL Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


MEPHOBARBITAL Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 0)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate

115-38-8()Verwandte Suche:


  • METHYLPHENOBARBITAL
  • MEPHOBARBITAL
  • 1-Methyl-5-ethyl-5-phenylbarbituric acid
  • 1-methyl-5-ethyl-5-phenylbarbituricacid
  • 1-Methyl-5-ethyl-5-phenyl-pyrimidine-2,4,6-trione
  • 1-Methyl-5-phenyl-5-ethylbarbituric acid
  • 1-methyl-5-phenyl-5-ethylbarbituricacid
  • 1-Methylphenobarbital
  • 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-1-methyl-5-phenyl-
  • 5-ethyl-1-methyl-5-phenyl-2,4,6-(1h,3h,5h)-pyrimidinetrione
  • 5-Ethyl-1-methyl-5-phenyl-2,4,6(1H,3H,5H)-pyrimidinetrione
  • 5-Ethyl-1-methyl-5-phenylbarbituric acid
  • 5-ethyl-1-methyl-5-phenyl-barbituricaci
  • 5-ethyl-1-methyl-5-phenylbarbituricacid
  • 5-Ethyl-5-phenyl-N-methyl-bartituric acid
  • 5-ethyl-5-phenyl-n-methyl-bartituricacid
  • 5-Ethyl-N-methyl-5-phenylbarbituric acid
  • 5-ethyl-n-methyl-5-phenylbarbituricacid
  • 5-Phenyl-5-ethyl-3-methylbarbituric acid
  • 5-phenyl-5-ethyl-3-methylbarbituricacid
  • 6(1h,3h,5h)-pyrimidinetrione,5-ethyl-1-methyl-5-phenyl-4
  • Barbituric acid, 5-ethyl-1-methyl-5-phenyl-
  • barbituricacid,5-ethyl-1-methyl-5-phenyl-
  • Enfenemal
  • Enphenemal
  • Hexahydropyrimidine-2,4,6-trione,1-methyl-5-ethyl-5-phenyl-
  • Isonal (Roussel)
  • isonal(roussel)
  • Mebaral
  • Meberal
  • Menta-bal
  • Mephobarbitone
  • Mephobsrbital
  • Mephytal
  • Methyl phenobarbitone
  • Methyl-calminal
  • methylphenobarbitone
  • methylphenolbarbital
  • Methylphenylbarbituric acid
  • methylphenylbarbituricacid
  • Metylfenemal
  • Metyna
  • Morbusan
  • N-Ethylmethylphenylbarbituric acid
  • n-ethylmethylphenylbarbituricacid
  • N-Methyl-5-phenyl-5-ethylbarbital
  • N-Methyl-5-phenyl-5-ethylbarbituric acid
  • N-Methylethylphenylbarbituric acid
  • n-methylethylphenylbarbituricacid
  • N-Methylphenobarbital
  • N-Methylphenolbarbitol
  • Phemetone
  • Phemiton
  • Phemitone
  • phenmiton
  • Phenobarbital, mono-methyl
  • Prominal
  • METHYLPHENOBARITAL
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