Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HCID 3261Erstellt: 24. Oktober 2026

Estazolam

ProSom · 8-CHLORO-6-PHENYL-4H-[1,2,4]-TRIAZOLO[4,3-A][1,4]BENZODIAZEPINE · u33737 · Cannoc · D 40TA · d-40ta · Nemurel · Julodin

https://huagongshe.com/de/chemical/3261

Molekülstruktur von Estazolam

Identifikatoren & physikalische Daten

CAS No.29975-16-4
SummenformelC16H11ClN4
Durchschnittliche Molmasse294,74 g/mol
Monoisotopische Masse294,06722403 g/mol
SMILESClc1ccc2c(c1)C(c1ccccc1)=NCc1nncn1-2
InChIKeyCDCHDCWJMGXXRH-UHFFFAOYSA-N
PubChem CID3261
ChEMBLCHEMBL285674
ChEBICHEBI:4858
EC No.249-982-4
DTXSIDDTXSID5020572
Lokaler NameEstazolam

Chemische & physikalische Eigenschaften

XLogP1,7
Polarare Oberfläche (TPSA)43,1
H-Brücken-Donoren0
H-Brücken-Akzeptoren3
Frei drehbare Bindungen1
Schwere Atome21
Formalladung0
Komplexität407
ArzneimittelDEA NFLIS-Drug Category -> BenzodiazepinesDEA Schedule IV Controlled Substance -> DepressantsPharmaceuticals -> Synthetic Cannabinoids or Psychoactive CompoundsPharmaceuticals -> BenzodiazepinesPharmaceuticals -> Listed in ZINC15
LogP (Verteilungskoeffizient)4.7
LöslichkeitPractically insoluble (1.5 mg/L)4.23e-02 g/LDMF: 30 mg/mlDMF:PBS(pH 7.2)(1:1): 0.5 mg/mlDMSO: 20 mg/mlEthanol: 10 mg/ml
Human DrugsBreast FeedingLactationMilk, HumanBenzodiazepinesHypnotics and SedativesFDA approved drugs -> Active ingredientPharmaceuticals
Schmelzpunkt228-229228.5 °C228-229°
Physical DescriptionSolid
Collision Cross Section168.1 Ų [M+H]+ [CCS Type: DTMethod: single field calibrated]
Siedepunkt448.04°C (rough estimate)
Dichte1.2294 (rough estimate)
Brechungsindex1.6110 (estimate)
Flammpunkt11 °C
Lagerbedingungen2-8°C
AggregatzustandA crystalline solid
pKa (Säurekonstante)pKa 2.84(H2O) (Uncertain)
CAS Datenbank29975-16-4(CAS DataBase Reference)
NIST chemische InformationenEstazolam(29975-16-4)

Sicherheit & Vorschriften

GHS-EinstufungThis chemical does not meet GHS hazard criteria for 2.3% (1 of 44) of reports.WarningH315 (93.2%): Causes skin irritation [Warning Skin corrosion/irritation]P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 44 reports by companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Regulatorische InformationenDEA schedule IV controlled substance4H-1,2,4Triazolo4,3-a1,4benzodiazepine, 8-chloro-6-phenyl-: Does not have an individual approval but may be used under an appropriate group standard
Hazard Classes and CategoriesSkin Irrit. 2 (93.2%)
TreatmentGastric evacuation, either by the induction of emesis, lavage, or both, should be performed immediately. Maintenance of adequate ventilation is essential. General supportive care, including frequent monitoring of the vital signs and close observation of the patient, is indicated. Fluids should be administered intravenously to maintain blood pressure and encourage diuresis. The value of dialysis in treatment of benzodiazepine overdose has not been determined. The physician may wish to consider contacting a Poison Control Center for up-to-date information on the management of hypnotic drug product overdose. Flumazenil, a specific benzodiazepine receptor antagonist, is indicated for the complete or partial reversal of the sedative effects of benzodiazepines and may be used in situations when an overdose with a benzodiazepine is known or suspected. (L1712)
Gesundheitliche AuswirkungenMay cause a potentially dangerous rash that may develop into Stevens Johnson syndrome, an extremely rare but potentially fatal skin disease.
HepatotoxicityEstazolam, as with other benzodiazepines, is rarely associated with serum ALT elevations, and clinically apparent liver injury from estazolam is extremely rare, if it occurs at all. There have been no published case reports of symptomatic, acute liver injury from estazolam. Isolated cases of clinically apparent hepatitis have been reported with other benzodiazepines including alprazolam, chlordiazepoxide, clonazepam, diazepam, flurazepam, lorazepam, and triazolam. The clinical pattern of acute liver injury from benzodiazepines is typically cholestatic and mild-to-moderate in severity with a latency of 1 to 6 months and full recovery within 1 to 2 months. Fever and rash have not been described nor has autoantibody formation.
ExpositionspfadeTablets have been found to be equivalent in absorption to an orally administered solution of estazolam. In healthy subjects who received up to three times the recommended dose, peak estazolam plasma concentrations occurred within two hours after dosing (range 0.5 to 6.0 hours) and were proportional to the administered dose, suggesting linear pharmacokinetics over the dosage range tested.
ToxizitätsübersichtBenzodiazepines bind nonspecifically to benzodiazepine receptors, which affects affects muscle relaxation, anticonvulsant activity, motor coordination, and memory. As benzodiazepine receptors are thought to be coupled to gamma-aminobutyric acid-A (GABA<sub>A</sub>) receptors, this enhances the effects GABA by increasing GABA affinity for the GABA receptor. Binding of the inhibitory neurotransmitter GABA to the site opens the chloride channel, resulting in a hyperpolarized cell membrane that prevents further excitation of the cell.
Signs and SymptomsSymptoms of overdose include confusion, depressed breathing, drowsiness and eventually coma, lack of coordination, and slurred speech.
Carcinogen ClassificationEstazolamGroup 3: Not classifiable as to its carcinogenicity to humansVolume 66: (1996) Some Pharmaceutical Drugs3, not classifiable as to its carcinogenicity to humans. (L135)
Drug Induced Liver InjuryDrug Induced Liver Injury Rank (DILIrank 2.0)EstazolamvNo-DILI-concernNo matchDOI:10.1016/j.drudis.2016.02.015
Effects During Pregnancy and Lactation◉ Summary of Use during Lactation◈ What is estazolam?
Toxicity DataLD50: 740 mg/kg (oral, male mice) (L1867) LD50: 3200 mg/kg (oral, rat) (L1867) LD50 300 mg/kg (oral, rabbit) (L1867)
Wassergefährdungsklasse (WGK)3
UN-Transportnummer3249
Zollcode2933910000
RTECS-Nr.XZ5473500
R-Sätze (R)36/37/38-39/23/24/25-23/24/25-11
ToxizitätLD50 orally in male mice, rats and rabbits: 740, 3200, 300 mg/kg (Yokotani)
GefahrensymboleXi,T,F
Sicherheitshinweise (S)36/37/39-45-36/37-16-7
Gefahrenklasse6.1(b)
VerpackungsgruppeIII

Anwendungen & Verwendung

Verwenden

A benzodiazepine derivative possessing anxiolytic, anticonvulsant, and muscle relaxant properties. It is commonly prescribed to treat short-term insomnia. Controlled Substance.