熔點174°C

沸點bp0.1 160°

密度0.9935 (rough estimate)

折射率1.5640 (estimate)

儲存條件Storage temp. 2-8°C

酸度系數(shù)(pKa)pKa 9.66(H2O,t = 25,I=0.025) (Uncertain)

形態(tài)Liquid

顏色Colorless to light yellow

水溶解性18.23mg/L(24 ºC)

Concentration1 mCi/ml

SolventEthanol under nitrogen

Specific Activity60-90 Ci/mmol

BCS Class1

警示詞危險

REACH 注冊登記Active

毒性A tertiary amine tricyclic antidepressant that is thought to exert its therapeutic effect by inhibiting the reuptake of serotonin and norepinephrine centrally. A major metabolite is N-desmethylimipramine (desipramine), also used as an antidepressant drug. Desipramine differs from imipramine in being a better blocker of norepinephrine, rather than serotonin, uptake. Side effects, including sedation and drowsiness, dry mouth, urinary retention, constipation, and orthostatic hypotension, are probably due to the anticholinergic, anti-α-adrenergic, and antihistaminergic receptor-blocking properties. Imipramine should not be used in conjunction with a monoamine oxidase inhibitor or other treatment that increases catecholamine concentrations (e.g., drugs containing sympathomimetic amines). Imipramine should be avoided in patients with cardiovascular disease or seizure disorder, or in those who may abuse alcohol, as imipramine lowers seizure threshold, can produce cardiovascular toxicity and may potentiate the effects of alcohol. Imipramine intoxication can include CNS abnormalities (e.g., drowsiness, stupor, coma, and extrapyramidal symptoms), cardiac arrhythmia, and respiratory depression. Children appear to be particularly vulnerable to the cardiotoxic and seizure-inducing effects of high doses of imipramine. The oral LD50 in female rats is 305 mg/kg.