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Home > products > Heptanoic acid,2-[4-[3-[2-(trifluoromethyl)-10H-phenothiazin-10-yl]propyl]-1-piperazinyl]ethylester

Heptanoic acid,2-[4-[3-[2-(trifluoromethyl)-10H-phenothiazin-10-yl]propyl]-1-piperazinyl]ethylester cas no:2746-81-8

Synonyms: Heptanoicacid, 2-[4-[3-[2-(trifluoromethyl)phenothiazin-10-yl]propyl]-1-piperazinyl]ethylester (7CI,8CI); 1-Piperazineethanol,4-[3-[2-(trifluoromethyl)phenothiazin-10-yl]propyl]-, heptanoate (ester) (8CI);4-[3-(2-Trifluoromethyl-10-phenothiazinyl)propyl]-1-piperazineethanolenanthate; Fluphenazine enanthate; Moditen enanthate; Prolixin enanthate; SQ16,114; SQ 16144

Identification
NameHeptanoic acid,2-[4-[3-[2-(trifluoromethyl)-10H-phenothiazin-10-yl]propyl]-1-piperazinyl]ethylester
CAS2746-81-8
SynonymsHeptanoicacid, 2-[4-[3-[2-(trifluoromethyl)phenothiazin-10-yl]propyl]-1-piperazinyl]ethylester (7CI,8CI); 1-Piperazineethanol,4-[3-[2-(trifluoromethyl)phenothiazin-10-yl]propyl]-, heptanoate (ester) (8CI);4-[3-(2-Trifluoromethyl-10-phenothiazinyl)propyl]-1-piperazineethanolenanthate; Fluphenazine enanthate; Moditen enanthate; Prolixin enanthate; SQ16,114; SQ 16144
EINECS(EC#)220-385-0
Molecular FormulaC29H38 F3 N3 O2 S
Molecular Weight549.76
Chemical Properties
refractive index1.544
Globally Harmonized System of Classification adn Labelling of Chemicals(GHS)
Hazardclass6.1(b)
Safety Data

Safety

Poison by intravenous, intramuscular, intraperitoneal, and subcutaneous routes. Human systemic effects by subcutaneous route: muscle weakness; by intramuscular route: musculo-skeletal changes. When Prolixin enanthate (CAS NO.2746-81-8) is heated to decomposition, it emits very toxic fumes of F, SOx, and NOx.

RIDADR: 3249
HazardClass: 6.1(b)
PackingGroup: III


Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
human TDLo intramuscular 1633ug/kg (1.633mg/kg) MUSCULOSKELETAL: OTHER CHANGES British Medical Journal. Vol. 2, Pg. 1071, 1966.
human TDLo subcutaneous 357ug/kg (0.357mg/kg) BEHAVIORAL: MUSCLE WEAKNESS American Journal of Psychiatry. Vol. 119, Pg. 779, 1963.
mouse LD50 intramuscular 17200ug/kg (17.2mg/kg)   Drugs in Japan Vol. 6, Pg. 701, 1982.
mouse LD50 intraperitoneal 300mg/kg (300mg/kg)   Drugs in Japan Vol. 6, Pg. 701, 1982.
mouse LD50 intravenous 56mg/kg (56mg/kg)   U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#03337,
mouse LD50 oral 41300ug/kg (41.3mg/kg)   Gekkan Yakuji. Pharmaceuticals Monthly. Vol. 11, Pg. 1421, 1969.
mouse LD50 subcutaneous 50mg/kg (50mg/kg)   Drugs in Japan Vol. 6, Pg. 701, 1982.
rat LD50 intraperitoneal 230mg/kg (230mg/kg)   Gekkan Yakuji. Pharmaceuticals Monthly. Vol. 11, Pg. 1421, 1969.
rat LD50 oral 230mg/kg (230mg/kg)   Gekkan Yakuji. Pharmaceuticals Monthly. Vol. 11, Pg. 1421, 1969.
rat LD50 subcutaneous 475mg/kg (475mg/kg)   Gekkan Yakuji. Pharmaceuticals Monthly. Vol. 11, Pg. 1421, 1969.
women TDLo intramuscular 250ug/kg (0.25mg/kg) BRAIN AND COVERINGS: CHANGES IN SURFACE EEG

BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX)

BEHAVIORAL: COMA
Italian Journal of Neurological Sciences. Vol. 1, Pg. 193, 1980.

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