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HCID 62920Erstellt: 27. Oktober 2026

Diltiazem hydrochloride

DILTIAZEM HCL · DILTHIAZEM HYDROCHLORIDE · Tiazac · herbesser · Diltiazem Hydrochlorid · Sprix · Acuvail · cardizem

https://huagongshe.com/de/chemical/62920

Molekülstruktur von Diltiazem hydrochloride

Identifikatoren & physikalische Daten

CAS No.33286-22-5
SummenformelC22H27ClN2O4S
Durchschnittliche Molmasse451 g/mol
Monoisotopische Masse450,13800602 g/mol
SMILESCOc1ccc([C@@H]2Sc3ccccc3N(CCN(C)C)C(=O)[C@@H]2OC(C)=O)cc1.Cl
InChIKeyHDRXZJPWHTXQRI-BHDTVMLSSA-N
PubChem CID62920
ChEMBLCHEMBL1697
ChEBICHEBI:645509
EC No.251-443-3
DTXSIDDTXSID8040147
Lokaler NameDiltiazem hydrochloride

Chemische & physikalische Eigenschaften

Polarare Oberfläche (TPSA)84,4
H-Brücken-Donoren1
H-Brücken-Akzeptoren6
Frei drehbare Bindungen7
Schwere Atome30
Formalladung0
Komplexität565
Human DrugsBreast FeedingLactationMilk, HumanAntihypertensive AgentsCalcium Channel BlockersAntiarrhythmicsVasodilator AgentsFDA approved drugs -> Active ingredient
Collision Cross Section196.1 Ų [M+H]+ [CCS Type: TWMethod: calibrated with polyalanine and drug standards]
Schmelzpunkt212-214 °C
Dichte1.30 g/cm3
Brechungsindex118 ° (C=1, H2O)
Flammpunkt2℃
Lagerbedingungen2-8°C
LöslichkeitFreely soluble in water, in methanol and in methylene chloride, slightly soluble in anhydrous ethanol.
AggregatzustandPowder
FarbeWhite to off-white
pHpH (10g/l, 25℃) : 4.3~5.3
Merck13,3226
BRN4228706
StabilitätStable for 1 year from date of purchase as supplied. Solutions in DMSO or distilled water may be stored at -20°C for up to 3 months.
Kosmetik-Inhaltsstoffe FunktionenASTRINGENTSKIN PROTECTING
InChI1S/C22H26N2O4S.ClH/c1-15(25)28-20-21(16-9-11-17(27-4)12-10-16)29-19-8-6-5-7-18(19)24(22(20)26)14-13-23(2)3/h5-12,20-21H,13-14H2,1-4H31H/t20-,21+/m1./s1
InChIKeyHDRXZJPWHTXQRI-BHDTVMLSSA-N
SMILESCl.COc1ccc(cc1)[C@@H]2Sc3ccccc3N(CCN(C)C)C(=O)[C@@H]2OC(C)=O
CAS Datenbank33286-22-5(CAS DataBase Reference)
EPA chemische Informationen1,5-Benzothiazepin-4(5H)-one, 3-(acetyloxy)-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-, hydrochloride (1:1), (2S,3S)- (33286-22-5)

Sicherheit & Vorschriften

GHS-EinstufungWarningH302 (99.2%): Harmful if swallowed [Warning Acute toxicity, oral]P203, P264, P270, P280, P301+P317, P318, P330, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 119 reports by companies from 16 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Regulatorische InformationenHazard Traits - Developmental ToxicityDiltiazem hydrochloride: Does not have an individual approval but may be used under an appropriate group standard
Weitere SicherheitsinformationenIMAP assessments - 1,5-Benzothiazepin-4(5H)-one, 3-(acetyloxy)-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-, monohydrochloride, (2S-cis)-: Environment tier I assessment
Hazard Classes and CategoriesAcute Tox. 4 (99.2%)
TreatmentIn the event of overdose or exaggerated response, appropriate supportive measures should be employed in addition to gastrointestinal decontamination. If bradycardia and/or high-degree AV block occurs, administer atropine (0.60 to 1.0 mg). If there is no response to vagal blockage, administer isoproterenol cautiously. Fixed high-degree AV block should be treated with cardiac pacing. In cases of cardiac failure, administer inotropic agents (isoproterenol, dopamine, or dobutamine) and diuretics. If hypotension occurs, use vasopressors (e.g. dopamine or levarterenol bitartrate). (L1712)
Gesundheitliche AuswirkungenBecause of its negative inotropic effect, diltiazem causes a modest decrease in heart muscle contractility and reduces myocardium oxygen consumption. Its negative chronotropic effect results in a modest lowering of heart rate, due to slowing of the sinoatrial node. It results in reduced myocardium oxygen consumption. Because of its negative dromotropic effect, conduction through the AV (atrioventricular) node is slowed, which increases the time needed for each beat. This results in reduced myocardium oxygen consumption. A reflex sympathetic response, caused by the peripheral dilation of vessels and the resulting drop in blood pressure, works to counteract the negative inotropic, chronotropic and dromotropic effects of diltiazem. Undesirable effects include hypotension, bradycardia, dizziness, and flushing. (Wikipedia)
Expositionspfade

Anwendungen & Verwendung

Verwenden

An antianginal, antihypertensive. Regulates Calcium release from intracellular stores in neutrophils

Intravenous, Oral. Diltiazem is well absorbed from the gastrointestinal tract but undergoes substantial hepatic first-pass effect.
ToxizitätsübersichtPossibly by deforming the channel, inhibiting ion-control gating mechanisms, and/or interfering with the release of calcium from the sarcoplasmic reticulum, diltiazem, like verapamil, inhibits the influx of extracellular calcium across both the myocardial and vascular smooth muscle cell membranes. The resultant inhibition of the contractile processes of the myocardial smooth muscle cells leads to dilation of the coronary and systemic arteries and improved oxygen delivery to the myocardial tissue.
Signs and SymptomsLD<sub>50</sub>=740mg/kg (orally in mice)
Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).
Drug Induced Liver InjuryDrug Induced Liver Injury Rank (DILIrank 2.0)Diltiazem hydrochloridevMost-DILI-concern4Warnings & precautionsDOI:10.1016/j.drudis.2016.02.015
Effects During Pregnancy and Lactation◉ Summary of Use during Lactation
Toxicity DataLD<sub>50</sub>=740mg/kg (orally in mice)
F8-10
Wassergefährdungsklasse (WGK)3
UN-Transportnummer3249
Zollcode29349990
RTECS-Nr.DL0310000
R-Sätze (R)22-40-36/37/38-36-20/21/22-11
ToxizitätLD50 in male, female mice, male, female rats (mg/kg): 61, 58, 38, 39 i.v.260, 280, 520, 550 s.c.740, 640, 560, 610 orally (Nagao, 1972)
GefahrensymboleXn,Xi,F
Sicherheitshinweise (S)36-45-36/37-26-16
Gefahrenklasse6.1(b)Acute Tox. 4 Oral
VerpackungsgruppeIII
Lagerklasse11 - Combustible Solids