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Imipramine

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Name

Imipramine

EINECS N/A
CAS No. 50-49-7 Density 1.041g/cm3
PSA 6.48000 LogP 3.94000
Solubility 18.23mg/L(24 oC) Melting Point 174°C
Formula C19H24 N2 Boiling Point 403.1°Cat760mmHg
Molecular Weight 280.413 Flash Point 179.7°C
Transport Information N/A Appearance N/A
Safety A human poison by ingestion. An experimental poison by ingestion, subcutaneous, intravenous, and intraperitoneal routes. Human systemic effects by ingestion: somnolence, hallucinations, distorted perceptions, changes in motor activity, ataxia (loss of muscle coordination), coma, nausea and vomiting, irritative dermatitis. An experimental teratogen by ingestion. Other experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx. Risk Codes N/A
Molecular Structure Molecular Structure of 50-49-7 (IMIPRAMINE) Hazard Symbols N/A
Synonyms

5H-Dibenz[b,f]azepine,5-[3-(dimethylamino)propyl]-10,11-dihydro- (7CI,8CI); 1-(3-Dimethylaminopropyl)-4,5-dihydro-2,3,6,7-dibenzazepine;5,6-Dihydro-N-[3-(dimethylamino)propyl]-11H-dibenz[b,e]azepine;5-(3-Dimethylaminopropyl)-10,11-dihydro-5H-dibenz[b,f]azepine; Antideprin;Berkomine; Cristalia; Imipramine; Melipramine; N-(3-Dimethylaminopropyl)-o-iminodibenzyl;N-(g-Dimethylaminopropyl)iminodibenzyl;NSC 169866; Org 2463; Prazepine; Sermonil

Article Data 30

Imipramine Synthetic route

6829-98-7

imipramine N-oxide

50-49-7

impramine

Conditions
ConditionsYield
With sodium tetrahydroborate In water at 50 - 60℃; chemoselective reaction;96%
50-47-5

desipramine

124-38-9

carbon dioxide

50-49-7

impramine

Conditions
ConditionsYield
With hydrogen In octane at 150℃; for 30h; Autoclave;89%
With hydrogen; tris(acetylacetonato)ruthenium(III); lithium chloride; [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine] In tetrahydrofuran at 140℃; for 24h; Autoclave; Inert atmosphere;83 %Chromat.
With proazaphosphatrane; 9-bora-bicyclo[3.3.1]nonane In tetrahydrofuran at 90℃; under 750.075 Torr; for 1h; Inert atmosphere; Schlenk technique; chemoselective reaction;99 %Spectr.
876124-39-9

N'-(4-carbomethoxy)desimipramine

50-49-7

impramine

Conditions
ConditionsYield
With lithium aluminium tetrahydride In tetrahydrofuran for 0.5h; Heating;79%
50-00-0

formaldehyd

2095-95-6

didesmethylimipramine

50-49-7

impramine

Conditions
ConditionsYield
With formic acid In water at 100℃; for 1h; Eschweiler-Clark Amine Methylation; Microwave irradiation;61%
59485-34-6

1,2-bis(2-bromophenyl)ethane

109-55-7

1-amino-3-(dimethylamino)propane

50-49-7

impramine

Conditions
ConditionsYield
With tris-(dibenzylideneacetone)dipalladium(0); sodium t-butanolate; XPhos In toluene at 110℃; Buchwald-Hartwig Coupling;60%
67-56-1

methanol

50-47-5

desipramine

50-49-7

impramine

Conditions
ConditionsYield
With rhodium(III) chloride hydrate; potassium tert-butylate at 150℃; for 60h; Sealed tube; High pressure;49%
303-49-1

Clomipramine

A

14171-67-6

clomipramine N-oxide

B

50-49-7

impramine

C

3-hydroxyimipramine

D

3-hydroxyimipramine-N-oxide

Conditions
ConditionsYield
With oxygen In methanol; phosphate buffer at 25 - 28℃; pH=7.4; Product distribution; Further Variations:; Reagents; Photolysis; UV-irradiation;A 15%
B 15%
C 40%
D 20%
494-19-9

9,10-dihydrodibenzazepine

50-49-7

impramine

Conditions
ConditionsYield
With sodium amide; benzene und Erwaermen der Reaktionsloesung mit <3-Chlor-propyl>-dimethyl-amin;
494-19-9

9,10-dihydrodibenzazepine

109-54-6

3-(Dimethylamino)propyl chloride

50-49-7

impramine

Conditions
ConditionsYield
With sodium hydroxide; potassium carbonate DMSO 1.) room temp., 2 h, 2.) 110 deg C, 18 h; Yield given. Multistep reaction;
With potassium hydroxide; ammonium acetate In toluene at 20℃; Heating / reflux;
124-38-9

carbon dioxide

[3-(10,11-Dihydro-dibenzo[b,f]azepin-5-yl)-propyl]-methyl-trimethylsilanyl-amine

50-49-7

impramine

Conditions
ConditionsYield
With lithium aluminium tetrahydride 1.) THF, -45 deg C - 60 deg C, 2.) 60 deg C, 10 min; Yield given. Multistep reaction;

Imipramine Chemical Properties

Molecular Structure of Imipramine (CAS NO.50-49-7):

Molecular Formula: C19H24N2
Molecular Weight: 280.41
IUPAC Name: 3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)-N,N-Dimethylpropan-1-amine
Synonyms of Imipramine (CAS NO.50-49-7): Imipramine ; Aurora ka-7708 ; 1-(3-Dimethylaminopropyl)-4,5-dihydro-2,3,6,7-dibenzazepine ; 10,11-Dihydro-5-(3-(dimethylamino)propyl)-5H-dibenz[b,f]azepine ; 2,2'-(3-Dimethylaminopropylimino)bibenzyl ; 2,2'-(3-Dimethylaminopropylimino)dibenzyl ; 3-(10,11-Dihydro-5H-dibenzo[b,f]azepin-5-yl)-N,N-dimethyl-1-propanamine ; 5-(3-(Dimethylamino)propyl)-10,11-dihydro-5H-dibenz(b,f)azepine
CAS NO: 50-49-7
EINECS: 200-042-1
Mol File: 50-49-7.mol
Index of Refraction: 1.574
Surface Tension: 40.1 dyne/cm
Density: 1.041 g/cm3
Flash Point: 179.7 °C
Enthalpy of Vaporization: 65.43 kJ/mol
Boiling Point: 403.1 °C at 760 mmHg
Vapour Pressure: 1.04E-06 mmHg at 25°C
Properties: white or light yellow crystalline powder, no smell, taste and burning hemp.
Solubility: soluble in water, ethanol; almost insoluble in ether.

Imipramine Uses

 Imipramine (CAS NO.50-49-7) is commonly used as antidepressants of tricyclic .

Imipramine Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
cat LDLo intravenous 20mg/kg (20mg/kg)   Bollettino Chimico Farmaceutico. Vol. 112, Pg. 601, 1973.
cat LDLo oral 100mg/kg (100mg/kg)   Zentralblatt fuer Pharmazie, Pharmakotherapie und Laboratoriums-diagnostik. Vol. 114, Pg. 787, 1975.
child LD50 oral 40mg/kg (40mg/kg) BEHAVIORAL: "HALLUCINATIONS, DISTORTED PERCEPTIONS"

BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY)

BEHAVIORAL: COMA
Handbook of Experimental Pharmacology. Vol. 55, Pg. 527, 1980.
child LDLo oral 35mg/kg (35mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: DYSPNEA

CARDIAC: OTHER CHANGES
Schweizerische Medizinische Wochenschrift. Vol. 99, Pg. 1157, 1969.
child TDLo oral 30mg/kg (30mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY)

BEHAVIORAL: ATAXIA
American Journal of Diseases of Children. Vol. 130, Pg. 507, 1976.
dog LDLo intravenous 45mg/kg (45mg/kg) PERIPHERAL NERVE AND SENSATION: FLACCID PARALYSIS WITHOUT ANESTHESIA (USUALLY NEUROMUSCULAR BLOCKAGE)

BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION
Bollettino Chimico Farmaceutico. Vol. 112, Pg. 601, 1973.
dog LDLo oral 100mg/kg (100mg/kg)   "Psychotropic Drugs and Related Compounds," 2nd ed., Usdin, E., and D.H. Efron, Washington, DC, 1972Vol. -, Pg. 78, 1972.
human LD50 oral 40mg/kg (40mg/kg)   Proceedings of the European Society for the Study of Drug Toxicity. Vol. 6, Pg. 171, 1965.
human LDLo oral 450mg/kg (450mg/kg) SKIN AND APPENDAGES (SKIN): "DERMATITIS, IRRITATIVE: AFTER SYSTEMIC EXPOSURE" British Medical Journal. Vol. 1, Pg. 722, 1979.
mammal (species unspecified) LD50 oral 350mg/kg (350mg/kg) BEHAVIORAL: ANTICONVULSANT Journal of Medicinal Chemistry. Vol. 8, Pg. 836, 1965.
mammal (species unspecified) LD50 unreported 455mg/kg (455mg/kg)   Khimiko-Farmatsevticheskii Zhurnal. Chemical Pharmaceutical Journal. For English translation, see PCJOAU. Vol. 24(7), Pg. 27, 1990.
man LD50 oral 30mg/kg (30mg/kg) BEHAVIORAL: "HALLUCINATIONS, DISTORTED PERCEPTIONS"

BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY)

BEHAVIORAL: COMA
Handbook of Experimental Pharmacology. Vol. 55, Pg. 527, 1980.
man LDLo oral 71mg/kg (71mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

CARDIAC: CHANGE IN RATE

ENDOCRINE: CHANGE IN LH
Journal of Toxicology, Clinical Toxicology. Vol. 19, Pg. 239, 1982.
man TDLo oral 5357ug/kg/5D- (5.357mg/kg) BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX)

BEHAVIORAL: CHANGE IN REM SLEEP (HUMAN)
Human Psychopharmacology. Vol. 11, Pg. 211, 1996.
man TDLo oral 8mg/kg/3D-I (8mg/kg) BEHAVIORAL: EXCITEMENT Lancet. Vol. 2, Pg. 568, 1959.
man TDLo oral 71428ug/kg/10 (71.428mg/kg) BEHAVIORAL: REGIDITY

SKIN AND APPENDAGES (SKIN): SWEATING: OTHER
Intensive Care Medicine. Vol. 23, Pg. 480, 1997.
mouse LD50 intraperitoneal 51600ug/kg (51.6mg/kg)   British Patent Document. Vol. #1460700,
mouse LD50 intravenous 21mg/kg (21mg/kg) AUTONOMIC NERVOUS SYSTEM: PARASYMPATHOLYTIC

BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY)

BEHAVIORAL: WAKEFULNESS
Archives Internationales de Pharmacodynamie et de Therapie. Vol. 245, Pg. 283, 1980.
mouse LD50 oral 188mg/kg (188mg/kg) SENSE ORGANS AND SPECIAL SENSES: PTOSIS: EYE

BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY)
Pharmaceutical Chemistry Journal Vol. 14, Pg. 773, 1980.
mouse LD50 subcutaneous 195ug/kg (0.195mg/kg) BEHAVIORAL: WAKEFULNESS Pharmaceutical Chemistry Journal Vol. 15, Pg. 412, 1981.
mouse LD50 unreported 107mg/kg (107mg/kg) AUTONOMIC NERVOUS SYSTEM: "SMOOTH MUSCLE RELAXANT (MECHANISM UNDEFINED, SPASMOLYTIC)" Journal of Medicinal Chemistry. Vol. 10, Pg. 418, 1967.
rabbit LD50 intravenous 18mg/kg (18mg/kg)   Archives Internationales de Pharmacodynamie et de Therapie. Vol. 120, Pg. 450, 1959.
rabbit LD50 oral 385mg/kg (385mg/kg)   Arzneimittel-Forschung. Drug Research. Vol. 19, Pg. 1617, 1969.
rat LD50 intraperitoneal 79mg/kg (79mg/kg)   Archives Internationales de Pharmacodynamie et de Therapie. Vol. 148, Pg. 560, 1964.
rat LD50 intravenous 9300ug/kg (9.3mg/kg)   United States Patent Document. Vol. #4141993,
rat LD50 oral 250mg/kg (250mg/kg) SENSE ORGANS AND SPECIAL SENSES: PTOSIS: EYE

BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY)
Pharmaceutical Chemistry Journal Vol. 14, Pg. 773, 1980.
rat LD50 subcutaneous 250mg/kg (250mg/kg)   Archives Internationales de Pharmacodynamie et de Therapie. Vol. 148, Pg. 560, 1964.
women LDLo oral 2mg/kg/1D (2mg/kg) LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES Journal of Pharmacy and Pharmacology. Vol. 16, Pg. 265, 1964.
women TDLo oral 3mg/kg/32H-I (3mg/kg) SKIN AND APPENDAGES (SKIN): PHOTOSENSITIVITY: AFTER SYSTEMIC EXPOSURE JAMA, Journal of the American Medical Association. Vol. 254, Pg. 357, 1985.
women TDLo oral 150mg/kg (150mg/kg) BEHAVIORAL: COMA

CARDIAC: OTHER CHANGES

VASCULAR: BP LOWERING NOT CHARACTERIZED IN AUTONOMIC SECTION
Journal of Toxicology, Clinical Toxicology. Vol. 33, Pg. 51, 1995.

Imipramine Consensus Reports

EPA Genetic Toxicology Program.

Imipramine Safety Profile

A human poison by ingestion. An experimental poison by ingestion, subcutaneous, intravenous, and intraperitoneal routes. Human systemic effects by ingestion: somnolence, hallucinations, distorted perceptions, changes in motor activity, ataxia (loss of muscle coordination), coma, nausea and vomiting, irritative dermatitis. An experimental teratogen by ingestion. Other experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.

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