Triazolam
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Triazolam Eigenschaften
- Schmelzpunkt:
- 209-212°C
- Siedepunkt:
- 499.51°C (rough estimate)
- Dichte
- 1.2835 (rough estimate)
- Brechungsindex
- 1.6300 (estimate)
- Flammpunkt:
- 11 °C
- storage temp.
- 2-8°C
- L?slichkeit
- DMF: 30 mg/ml; DMF:PBS(pH 7.2)(1:1): 0.5 mg/ml; DMSO: 20 mg/ml; Ethanol: 10 mg/ml
- Aggregatzustand
- A crystalline solid
- pka
- pKa 1.52(H2O) (Uncertain);6.5(H2O) (Uncertain)
- Wasserl?slichkeit
- 30mg/L(ambient temperature)
- CAS Datenbank
- 28911-01-5(CAS DataBase Reference)
- NIST chemische Informationen
- Triazolam(28911-01-5)
- EPA chemische Informationen
- Triazolam (28911-01-5)
Sicherheit
- Risiko- und Sicherheitserkl?rung
- Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher | F,T | ||
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R-S?tze: | 11-23/24/25-36/38-39/23/24/25 | ||
S-S?tze: | 22-24/25-26-36-45-36/37-16-7 | ||
RIDADR | 3249 | ||
WGK Germany | 2 | ||
RTECS-Nr. | XZ5472500 | ||
HazardClass | 6.1(b) | ||
PackingGroup | III | ||
HS Code | 2933910000 | ||
Giftige Stoffe Daten | 28911-01-5(Hazardous Substances Data) | ||
Toxizit?t | LD50 in mice, rats (mg/kg): >100, >5000 orally (Pharm. Weekblad.) |
Bildanzeige (GHS) |
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Sicherheit |
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Triazolam Chemische Eigenschaften,Einsatz,Produktion Methoden
R-S?tze Betriebsanweisung:
R11:Leichtentzündlich.R23/24/25:Giftig beim Einatmen, Verschlucken und Berührung mit der Haut.
R36/38:Reizt die Augen und die Haut.
R39/23/24/25:Giftig: ernste Gefahr irreversiblen Schadens durch Einatmen, Berührung mit der Haut und durch Verschlucken.
S-S?tze Betriebsanweisung:
S22:Staub nicht einatmen.S24/25:Berührung mit den Augen und der Haut vermeiden.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn m?glich, dieses Etikett vorzeigen).
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S16:Von Zündquellen fernhalten - Nicht rauchen.
S7:Beh?lter dicht geschlossen halten.
Chemische Eigenschaften
Yellow SolidVerwenden
TriazolamWeltgesundheitsorganisation (WHO)
Triazolam, a benzodiazepine derivative with sedative and hypnotic activity, was introduced in 1978 for themanagement of insomnia. It is controlled under Schedule IV of the 1971 Convention of Psychotropic Substances. Concern regarding the psychotropic effects of triazolam was first raised in the Netherlands in 1979 when this compound was suspended for sale and subsequently withdrawn by the Committee for the Evaluation of Medicines on the basis of reports of a reversible complex of symptoms including paranoia, depersonalization, nightmares, suicidal tendency and hyperaesthesia in patients receiving the drug. The basis for this decision was later successfully contested by the manufacturer and the drug was reregistered in early 1990 with a revised product information. However, concern was regenerated elsewhere that higher doses are associated with an unacceptable incidence of unwanted effects and the manufacturer has eventually withdrawn 0.5 mg tablets on a worldwide basis. In 1991 the issue of the safety of triazolam was again reopened by reports of retrograde amnesia and depression among patients taking the decreased recommended dosages. The product information has been revised by the United States FDA to include more rigorous cautions regarding dosage. In the Member States of the European Communities the products have been suspended pending further review by the EC Committee on Proprietary Medicinal Products.Allgemeine Beschreibung
Triazolam, 8-chloro-6-(o-chlorophenyl)-1-methyl-4H-s-triazolo[4,3-a][1,4] benzodiazepine(Halcion), has all of the characteristic benzodiazepine pharmacologicalactions. It is an ultra–short-acting hypnoticbecause it is rapidly α-hydroxylated to the 1-methyl alcohol,which is then rapidly conjugated and excreted.Consequently, it has gained popularity as sleep inducers, especiallyin elderly patients, because it causes less daytimesedation. It is metabolically inactivated primarily by hepaticand intestinal CYP3A4; therefore, coadministration withgrapefruit juice increases its peak plasma concentration by30%, leading to increased drowsiness.Triazolam Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
28911-01-5()Verwandte Suche:
Benzotriazol (in atembarer Form)
Basic Violet 1
Methylacrylat
Chlorzoxazon
Paraquat-dichlorid
Acetonitril
1,2,4-Triazol
Cloxacillinnatrium
Kresoxim-methyl
Methyltriphenylphosphoniumbromid
Methanol
1-CHLOROMETHYL-1H-1,2,4-TRIAZOLE
Methyl-4-hydroxybenzoat
Methylacetat
Dichlor(methyl)(phenyl)silan
5-Methyl-1H-benzotriazol
N,N,N-Trimethylaniliniumchlorid
Trazodon
- Triazolam CIV (200 mg)
- Triazolam solution
- TRIAZOLAM
- triazolam100ugpermlinmethanol
- U-33,030
- 8-CHLORO-6-(2-CHLOROPHENYL)-1-METHYL-4H-1,2,4-TRIAZOLO[4,3-A]1,4-BENZODIAZEPINE
- triazolam--dea schedule iv item
- TRIAZOLAM BENZODIAZEPINE ANXIOL
- 8-Chloro-1-methyl-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine
- D II-18-2
- Halcyon
- 8-Chloro-6-(o-chlorophenyl)-1-methyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine
- Asasion
- 4H-[1,2,4]Tr
- Triazolam,8-Chloro-6-[2-chlorophenyl]-1-methyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine
- Methanol(test Triazolam 1.0 mg/mL)
- 3-a)(1,4)benzodiazepine,8-chloro-6-(o-chlorophenyl)-1-methyl-4h-s-triazolo(
- 4h-(1,2,4)triazolo(4,3-a)(1,4)benzodiazepine,8-chloro-6-(2-chlorophenyl)-1-m
- 4H-[1,2,4]Triazolo[4,3-a][1,4]benzodiazepine, 8-chloro-6-(2-chlorophenyl)-1-methyl-
- 4H-s-Triazolo(4,3-a)(1,4)benzodiazepine, 8-chloro-6-(o-chlorophenyl)-1-methyl-
- 8-chloro-6-(2-chlorophenyl)-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazep
- 8-Chloro-6-(o-chlorophenyl)-1-methyl-4H-s-triazolo(4,3-a)(1,4)benzodiazepine
- clorazolam
- Halcion
- Halcion (triazolam)
- novidorm
- Novodorm
- Songar
- Triazolam USP/EP/BP
- Triazolam 13C D3
- Triazolam CIV (1680506)
- Triazolam (CRM)
- 28911-01-5
- C17H12Cl2N4
- API
- Aromatics, Heterocycles, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals
- Heterocycles
- Metabolites & Impurities
- Organics
- Intermediates & Fine Chemicals
- Pharmaceuticals
- Aromatics