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Clomipramine hydrochloride

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Name

Clomipramine hydrochloride

EINECS 241-344-3
CAS No. 17321-77-6 Density N/A
PSA 6.48000 LogP 5.39540
Solubility H2O: 25 mg/mL Melting Point 189-190 °C
Formula C19H23ClN2.HCl Boiling Point 434.2 °C at 760 mmHg
Molecular Weight 351.319 Flash Point 216.4 °C
Transport Information N/A Appearance off-white solid
Safety 36 Risk Codes 20/21/22
Molecular Structure Molecular Structure of 17321-77-6 (Clomipramine hydrochloride) Hazard Symbols HarmfulXn
Synonyms

5H-Dibenz[b,f]azepine,3-chloro-5-[3-(dimethylamino)propyl]-10,11-dihydro-, monohydrochloride (8CI);5H-Dibenz[b,f]azepine-5-propanamine, 3-chloro-10,11-dihydro-N,N-dimethyl-,monohydrochloride (9CI);3-Chloro-5-(3-dimethylaminopropyl)-10,11-dihydro-5H-dibenz[b,f]azepinehydrochloride;3-Chloroimipramine hydrochloride;Anafranil;Anaphranil;Anatranil;Chloroimipramine monohydrochloride;

Article Data 3

Clomipramine hydrochloride Specification

The Chlorimipramine hydrochloride with the cas number 17321-77-6, is also called (1)3-Chloro-5-(3-(dimethylamino)propyl)-10,11-dihydro-5H-dibenz(b,f)azepine monohydrochloride ; (2) 3-Chloroimipramine hydrochloride ; (3) 5H-Dibenz(b,f)azepine-5-propanamine, 3-chloro-10,11-dihydro-; (4)N,N-dimethyl-, monohydrochloride ; (5) Anafranil ; (6) Anaphranil ; (7) Chlorimipramine hydrochloride ; (8) Chloroimipramine monohydrochloride ; (9) Clomicalm ; (10) Clomipramine HCl ; (11) Clomipramine hydrochloride ; (12) EINECS 241-344-3 ; (13) G 34586 ; (14) Hydiphen ; (15) UNII-2LXW0L6GWJ. It belongs to the following product categories such as (1)Organics; (2)Chemical Amines; (3)Amines; (4)Heterocycles; (5)Intermediates & Fine Chemicals; (6)Pharmaceuticals; (7)Serotonin receptor. 

Properties of Venlafaxine are: (1)ACD/BCF (pH 5.5): 6.79 ; (2)ACD/BCF (pH 7.4): 76.21 ; (3)ACD/KOC (pH 5.5): 18.76 ; (4)ACD/KOC (pH 7.4): 210.7 ; (5)#H bond acceptors: 2 ; (6)#H bond donors: 0 ; (7)#Freely Rotating Bonds: 4 ; (8)Polar Surface Area: 6.48Å2 ; (9)Flash Point: 216.4 °C ; (10)Enthalpy of Vaporization: 69.03 kJ/mol ; (11)Boiling Point: 434.2 °C at 760 mmHg ; (12)Vapour Pressure: 9.63E-08 mmHg at 25°C

The Chlorimipramine hydrochloride appears to be off-White solid. It is used for serotonin reuptake inhibitor. antidepressant and antiobsessional agent. Chlorimipramine hydrochloride is quite harmful by inhalation, in contact with skin and if swallowed. Hence, in case of such dangerous thing, please wear suitable protective clothing.

You can still convert the following datas into molecular structure :
1. SMILES: Cl.Clc1ccc3c(c1)N(c2ccccc2CC3)CCCN(C)C
2. InChI: InChI=1/C19H23ClN2.ClH/c1-21(2)12-5-13-22-18-7-4-3-6-15(18)8-9-16-10-11-17(20)14-19(16)22;/h3-4,6-7,10-11,14H,5,8-9,12-13H2,1-2H3;1H

The Chlorimipramine hydrochloride toxic data can be showed in the following sheet.

  Test Type Route Reported Dose (Normalized Dose) Effect Source
dog LD50 intravenous 32mg/kg (32mg/kg)   Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 2105, 1970.
dog LD50 oral 383mg/kg (383mg/kg)   Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 2105, 1970.
dog LD50 subcutaneous > 400mg/kg (400mg/kg)   Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 2105, 1970.
mouse LD50 intraperitoneal 90mg/kg (90mg/kg)   Drugs in Japan Vol. 6, Pg. 243, 1982.
mouse LD50 intravenous 22mg/kg (22mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: CYANOSIS
European Journal of Pharmacology. Vol. 32, Pg. 108, 1975.
mouse LD50 oral 470mg/kg (470mg/kg)   Drugs in Japan Vol. 6, Pg. 243, 1982.
mouse LD50 subcutaneous 400mg/kg (400mg/kg)   Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 2105, 1970.
rabbit LD50 intravenous 12mg/kg (12mg/kg)   Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 2105, 1970.
rabbit LD50 oral 792mg/kg (792mg/kg)   Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 2105, 1970.
rabbit LD50 subcutaneous 217mg/kg (217mg/kg)   Kiso to Rinsho. Clinical Report. Vol. 4, Pg. 2105, 1970.
rat LD50 intraperitoneal 135mg/kg (135mg/kg)   Drugs in Japan Vol. 6, Pg. 243, 1982.
rat LD50 intravenous 26mg/kg (26mg/kg)   Drugs in Japan Vol. 6, Pg. 243, 1982.
rat LD50 oral 914mg/kg (914mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

LUNGS, THORAX, OR RESPIRATION: CYANOSIS
European Journal of Pharmacology. Vol. 32, Pg. 108, 1975.
rat LD50 subcutaneous 1750mg/kg (1750mg/kg)   Drugs in Japan Vol. 6, Pg. 243, 1982.
women LDLo oral 51mg/kg (51mg/kg) SENSE ORGANS AND SPECIAL SENSES: MYDRIASIS (PUPILLARY DILATION): EYE

BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

CARDIAC: PULSE RATE INCREASE WITHOUT FALL IN BP
Journal of Analytical Toxicology. Vol. 22, Pg. 612, 1998.
women TDLo oral 9mg/kg/9D-I (9mg/kg) AUTONOMIC NERVOUS SYSTEM: "SMOOTH MUSCLE RELAXANT (MECHANISM UNDEFINED, SPASMOLYTIC)"

BEHAVIORAL: ATAXIA

BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY)
American Journal of Psychiatry. Vol. 150, Pg. 165, 1993.
women TDLo oral 170mg/kg (170mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD

CARDIAC: EKG CHANGES NOT DIAGNOSTIC OF ABOVE

VASCULAR: BP LOWERING NOT CHARACTERIZED IN AUTONOMIC SECTION
Journal of Toxicology, Clinical Toxicology. Vol. 38, Pg. 447, 2000.
women TDLo oral 360mg/kg/13W- (360mg/kg) CARDIAC: PULSE RATE INCREASE WITHOUT FALL IN BP Journal of Clinical Psychiatry. Vol. 46, Pg. 290, 1985.

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