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59333-67-4

Basic Information
CAS No.: 59333-67-4
Name: Fluoxetine hydrochloride
Article Data: 33
Molecular Structure:
Molecular Structure of 59333-67-4 (Fluoxetine hydrochloride)
Formula: C17H18F3NO.HCl
Molecular Weight: 309.331
Synonyms: Methyl[3-phenyl-3-[4-(trifluoromethyl)phenoxy]propyl]amine hydrochloride;N-Methyl-gama-[4-(trifluoromethyl);Motivone;CCRIS 7093;Cramin;Depreks;Digassim;Felicium;Equilibrane;Fluoxetine HCl;
EINECS: 260-101-2
Density: 1.254g/cm3
Melting Point: 158-159 °C
Boiling Point: 395.1 °C at 760 mmHg
Flash Point: 192.8 °C
Solubility: water: 4 mg/mL
Appearance: white to off-white powder
Hazard Symbols: HarmfulXn
Risk Codes: 22-38-41
Safety: 26-36/37/39
PSA: 21.26000
LogP: 5.62790
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Chemistry

Molecular Formula: C17H19ClF3NO
Molecular Weight: 345.7871
EINECS: 260-101-2
Melting point: 158-159 °C
Water solubility: 4 mg/mL
Flash Point: 192.8 °C
Enthalpy of Vaporization: 64.52 kJ/mol
Boiling Point: 395.1 °C at 760 mmHg
Vapour Pressure: 1.88E-06 mmHg at 25 °C
Appearance: White to off-white powder
Structure of Fluoxetine hydrochloride (CAS NO.59333-67-4):
                         
IUPAC Name: N-Methyl-3-phenyl-3-[4-(trifluoromethyl)phenoxy]propan-1-aminehydrochloride
Product Category of Fluoxetine hydrochloride (CAS NO.59333-67-4): Active Pharmaceutical Ingredients;Fluorobenzene;APIs;Intermediates & Fine Chemicals;Serotonin receptor

History

According to David Wong, the work which eventually led to the discovery of fluoxetine began at Eli Lilly in 1970 as a collaboration between Bryan Molloy and Robert Rathbun. Testing the physiological effects of these compounds in mice resulted in nisoxetine, a selective norepinephrine reuptake inhibitor currently widely used in biochemical experiments. This test which carried out by Jong-Sir Horng in May 1972, showed the compound later named fluoxetine to be the most strong and selective inhibitor of serotonin reuptake of the series. Two years later they had to issue a correction, admitting that the first SSRI was zimelidine developed by Arvid Carlsson and colleagues. In 1986, Fluoxetine made its appearance on the Belgian market and was approved for use by the FDA in the United States in December 1987. Fluoxetine was the fourth SSRI to make it to market, after zimelidine, indalpine and fluvoxamine. 

Uses

 Fluoxetine hydrochloride (CAS NO.59333-67-4) can be used as an antidepressant.

Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
cat LD oral > 50mg/kg (50mg/kg)   Journal of Clinical Psychiatry. Vol. 46(3, Pg. Sec,
child TDLo oral 26mg/kg (26mg/kg) CARDIAC: EKG CHANGES NOT DIAGNOSTIC OF ABOVE
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
GASTROINTESTINAL: NAUSEA OR VOMITING
Journal of the American Academy of Child and Adolescent Psychiatry. Vol. 28, Pg. 587, 1989.
dog LD oral > 100mg/kg (100mg/kg)   Journal of Clinical Psychiatry. Vol. 46(3, Pg. Sec,
guinea pig LD oral > 250mg/kg (250mg/kg)   Journal of Clinical Psychiatry. Vol. 46(3, Pg. Sec,
human TDLo oral 7770ug/kg (7.77mg/kg) BEHAVIORAL: TREMOR
CARDIAC: ARRHYTHMIAS (INCLUDING CHANGES IN CONDUCTION)
GASTROINTESTINAL: NAUSEA OR VOMITING
American Journal of Emergency Medicine. Vol. 10, Pg. 115, 1992.
man TDLo oral 3733ug/kg/24H (3.733mg/kg) BEHAVIORAL: SLEEP
BEHAVIORAL: EUPHORIA
BEHAVIORAL: AGGRESSION
American Journal of Psychiatry. Vol. 143, Pg. 686, 1985.
man TDLo oral 12mg/kg/8W-I (12mg/kg) BEHAVIORAL: "HALLUCINATIONS, DISTORTED PERCEPTIONS" American Journal of Psychiatry. Vol. 150, Pg. 1750, 1993.
man TDLo oral 208mg/kg/2Y-I (208mg/kg) BEHAVIORAL: ANOREXIA (HUMAN
BEHAVIORAL: MUSCLE WEAKNESS
LIVER: "JAUNDICE, OTHER OR UNCLASSIFIED"
Mayo Clinic Proceedings. Vol. 74, Pg. 692, 1999.
monkey LD oral > 50mg/kg (50mg/kg)   Journal of Clinical Psychiatry. Vol. 46(3, Pg. Sec,
mouse LD50 intraperitoneal 100mg/kg (100mg/kg)   Toxicology and Applied Pharmacology. Vol. 32, Pg. 129, 1975.
mouse LD50 oral 248mg/kg (248mg/kg)   Journal of Clinical Psychiatry. Vol. 46(3, Pg. Sec,
rat LD50 oral 452mg/kg (452mg/kg)   Journal of Clinical Psychiatry. Vol. 46(3, Pg. Sec,
women TDLo oral 400ug/kg (0.4mg/kg) BEHAVIORAL: EXCITEMENT Journal of Clinical Psychiatry. Vol. 50, Pg. 339, 1989.
women TDLo oral 800ug/kg/2D-I (0.8mg/kg) CARDIAC: ARRHYTHMIAS (INCLUDING CHANGES IN CONDUCTION)
CARDIAC: PULSE RATE
Journal of Clinical Psychiatry. Vol. 52, Pg. 174, 1991.
women TDLo oral 2800ug/kg/1W- (2.8mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) Journal of Clinical Psychiatry. Vol. 55, Pg. 118, 1994.
women TDLo oral 5600ug/kg/2W- (5.6mg/kg) SKIN AND APPENDAGES (SKIN): HAIR: OTHER British Journal of Psychiatry. Vol. 159, Pg. 737, 1991.
women TDLo oral 5600ug/kg/2W- (5.6mg/kg) BEHAVIORAL: EXCITEMENT
BEHAVIORAL: HEADACHE
MUSCULOSKELETAL: CHANGES IN TEETH AND SUPPORTING STRUCTURES
Journal of Clinical Psychiatry. Vol. 54, Pg. 432, 1993.
women TDLo oral 8mg/kg/4W-I (8mg/kg) BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY)
BEHAVIORAL: HEADACHE
Journal of Clinical Psychiatry. Vol. 54, Pg. 235, 1993.
women TDLo oral 8400ug/kg/3W- (8.4mg/kg) CARDIAC: CHANGE IN RATE
VASCULAR: BP LOWERING NOT CHARACTERIZED IN AUTONOMIC SECTION
Annals of Emergency Medicine. Vol. 20, Pg. 194, 1991.
women TDLo oral 13600ug/kg (13.6mg/kg) SKIN AND APPENDAGES (SKIN): "DERMATITIS, ALLERGIC: AFTER SYSTEMIC EXPOSURE"
SKIN AND APPENDAGES (SKIN): "DERMATITIS, IRRITATIVE: AFTER SYSTEMIC EXPOSURE"
Journal of Toxicology, Clinical Toxicology. Vol. 27, Pg. 389, 1989.
women TDLo oral 17mg/kg/2W-I (17mg/kg) BEHAVIORAL: ANOREXIA (HUMAN Journal of Clinical Psychiatry. Vol. 55, Pg. 118, 1994.
women TDLo oral 28mg/kg/7W-I (28mg/kg) LUNGS, THORAX, OR RESPIRATION: DYSPNEA Medical Journal of Australia. Vol. 156, Pg. 364, 1992.

Safety Profile

Hazard Codes: Xn
Risk Statements: 22-38-41
22:Harmful if swallowed
38:Irritating to the skin
41:Risk of serious damage to eyes  
Safety Statements: 26-36/37/39
26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
36/37/39:Wear suitable protective clothing, gloves and eye/face protection

Specification

 Fluoxetine hydrochloride , its cas register number is 59333-67-4. It also can be called N-Methyl-gama-[4-(trifluoromethyl) ; and Methyl[3-phenyl-3-[4-(trifluoromethyl)phenoxy]propyl]amine hydrochloride .