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FLUPHENAZINE HYDROCHLORIDE

CAS No.
146-56-5
Chemical Name:
FLUPHENAZINE HYDROCHLORIDE
Synonyms
FLUPHENAZINE HCL;FLUPHENAZINE DIHYDROCHLORIDE;Prolinate;prolixin;anatensol;omca;a4077;liogen;moditen;mirenil
CBNumber:
CB4154808
Molecular Formula:
C22H28Cl2F3N3OS
Molecular Weight:
510.44
MDL Number:
MFCD00055212
MOL File:
146-56-5.mol
MSDS File:
SDS
Last updated:2023-06-06 18:14:08

FLUPHENAZINE HYDROCHLORIDE Properties

Melting point 200-2020C
storage temp. 2-8°C
solubility Soluble in DMSO and methanol.
color White to Light yellow
Sensitive Hygroscopic
Stability Hygroscopic
FDA UNII ZOU145W1XL
NCI Dictionary of Cancer Terms fluphenazine hydrochloride
NCI Drug Dictionary fluphenazine hydrochloride
EPA Substance Registry System Fluphenazine dihydrochloride (146-56-5)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS06,GHS08
Signal word  Danger
Hazard statements  H301-H360
Precautionary statements  P201-P280-P301+P330+P331+P310-P308+P313
Hazard Codes  Xn
Risk Statements  36/37/38-20/21/22
Safety Statements  26-36/37/39-36
RIDADR  UN2811
WGK Germany  3
RTECS  TL9800000
HazardClass  6.1
PackingGroup  III
HS Code  2934302300
Toxicity guinea pig,LD50,intraperitoneal,299mg/kg (299mg/kg),Pharmazie. Vol. 38, Pg. 749, 1983.
NFPA 704
1
2 1

FLUPHENAZINE HYDROCHLORIDE price More Price(33)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich F-903 Fluphenazine dihydrochloride solution 1.0?mg/mLinmethanol(asfreebase),ampuleof1?mL,certifiedreferencemateri 146-56-5 1mL $116 2024-03-01 Buy
Sigma-Aldrich BP167 Fluphenazine hydrochloride British Pharmacopoeia (BP) Reference Standard 146-56-5 100MG $229 2024-03-01 Buy
Sigma-Aldrich 1282004 Fluphenazine hydrochloride United States Pharmacopeia (USP) Reference Standard 146-56-5 125mg $358 2024-03-01 Buy
Sigma-Aldrich F4765 Fluphenazine dihydrochloride 146-56-5 1g $85.9 2023-06-20 Buy
TCI Chemical F1240 Fluphenazine Dihydrochloride 146-56-5 1G $42 2024-03-01 Buy
Product number Packaging Price Buy
F-903 1mL $116 Buy
BP167 100MG $229 Buy
1282004 125mg $358 Buy
F4765 1g $85.9 Buy
F1240 1G $42 Buy

FLUPHENAZINE HYDROCHLORIDE Chemical Properties,Uses,Production

Chemical Properties

Off-White Solid

Originator

Prolixin, Squibb ,US ,1959

Uses

antiandrogen, antineoplastic, Nuclear Hormone receptor antagonist

Uses

Antipsychotic

Definition

ChEBI: Fluphenazine hydrochloride is a member of phenothiazines. It has a role as an anticoronaviral agent.

Manufacturing Process

A suspension of 69.0 grams of 2-trifluoromethylphenothiazine in 1 liter of toluene with 10.9 grams of sodium amide is heated at reflux with high speed stirring for 15 minutes. A solution of 54.1 grams of 1-formyl-4-(3'chloropropyl)-piperazine, [prepared by formylating 1-(3'-hydroxypropyl)piperazine by refluxing in an excess of methyl formate, purifying the 1-formyl4-(3'-hydroxypropyl)-piperazine by vacuum distillation, reacting this compound with an excess of thionyl chloride at reflux and isolating the desired 1-formyl-4(3'-chloropropyl)-piperazine by neutralization with sodium carbonate solution followed by distillation] in 200 ml of toluene is added. The reflux period is continued for 4 hours. The cooled reaction mixture is treated with 200 ml of water. The organic layer is extracted twice with dilute hydrochloric acid. The acid extracts are made basic with ammonia and extracted with benzene. The volatiles are taken off in vacuo at the steam bath to leave a dark brown oil which is 10-[3'-(N-formylpiperazinyl)-propyl]-2trifluoromethylphenothiazine. It can be distilled at 260°C at 10 microns, or used directly without distillation if desired.
A solution of 103.5 grams of 10-[3'-(N-formylpiperazinyl)-propyl]-2trifluoromethylphenothiazine in 400 ml of ethanol and 218 ml of water containing 26 ml of 40% sodium hydroxide solution is heated at reflux for 2 hours. The alcohol is taken off in vacuo on the steam bath. The residue is swirled with benzene and water. The dried benzene layer is evaporated in vacuo. The residue is vacuum distilled to give a viscous, yellow oil, 10(3'piperazinylpropyl)-2-trifluoromethylphenothiazine, distilling at 210° to235°C at 0.5 to 0.6 mm.
A suspension of 14.0 grams of 10-(3'-piperazinylpropyl)-2trifluoromethylphenothiazine, 6.4 grams of β-bromoethyl acetate and 2.6 grams of potassium carbonate in 100 ml of toluene is stirred at reflux for 16 hours. Water (50 ml) is added to the cooled mixture. The organic layer is extracted into dilute hydrochloric acid. After neutralizing the extracts and taking the separated base up in benzene, a viscous, yellow residue is obtained by evaporating the organic solvent in vacuo. This oil is chromatographed on alumina. The purified fraction of 7.7 grams of 10-[3'-(Nacetoxyethylpiperazinyl)-propyl] -2-trifluoromethylphenothiazine is taken up in ethyl acetate and mixed with 25 ml of alcoholic hydrogen chloride. Concentration in vacuo separates white crystals of the dihydrochloride salt, MP 225° to 227°C.
A solution of 1.0 gram of 10-[3'-(N-acetoxyethylpiperazinyl)-propyl]-2trifluoromethylphenothiazine in 25 ml of 1 N hydrochloric acid is heated at reflux briefly. Neutralization with dilute sodium carbonate solution and extraction with benzene gives the oily base, 10-[3'-(N-βhydroxyethylpiperazinyl)-propyl]-2-trifluoromethylphenothiazine. The base is reacted with an excess of an alcoholic hydrogen chloride solution. Trituration with ether separates crystals of the dihydrochloride salt, MP 224° to 226°C, (from US Patent 3,058,979).

Therapeutic Function

Tranquilizer

General Description

The member ofthe piperazine subgroup with a trifluoromethyl group at the2-position of the phenothiazine system and the most potentantipsychotic phenothiazine on a milligram basis is fluphenazinehydrochloride, 4-[3-[2-(trifluoromethyl)phenazin-10-yl] propyl]-1-piperazineethanol dihydrochloride, 10[3-[4-(2-hydroxyethyl)piperazinyl]propyl]-2-trifluoromethylphenothiazine dihydrochloride (Permitil, Prolixin). It is alsoavailable as two lipid-soluble esters for depot intramuscularinjection, the enanthate (heptanoic acid ester) and the decanoateester. These long-acting preparations have use intreating psychotic patients who do not take their medicationor are subject to frequent relapse.

Biological Activity

ec50: 1.24 μmfluphenazine is a dopamine d1 and d2 receptor inhibitor.dopamine d1 and d2 receptor immunohistochemistry has been used to study the structure of the adult rat arcuate-median eminence complex, particularly in relation to the tubero-infundibular dopamine neurons.

Biochem/physiol Actions

D1/D2 dopamine receptor antagonist; phenothiazine antipsychotic; H1 histamine receptor antagonist.

in vitro

previous study showed that both phenothiazines of fluphenazine and perphenazine induced concentration-dependent loss in cell viability with ec50s to be 1.24 and 2.76 μm for fluphenazine and perphenazine, respectively. moreover, fluphenazine at 1.0 μm and perphenazine at 1.0 and 3.0 μm could inhibit melanogenesis and decrease the content of microphthalmia-associated transcription factor. in addition, both fluphenazine and perphenazine at higher concentrations caused depletion of melanocytes antioxidant status, indicating oxidative stress induction [1].

in vivo

systemic fluphenazine could effectively attenuate mechanical allodynia in rat neuropathic pain models at 0.03-0.3 mg/kg doses, which approximated those used in rodent models of psychosis. for antiallodynic effect, fluphenazine was able to effectively suppress the ectopic discharges in injured afferent fibers without affecting the propagation of action potentials in an ex-vivo drg-nerve preparation from cci rats [2].

References

[1] otreba m et al. fluphenazine and perphenazine impact on melanogenesis and antioxidant enzymes activity in normal human melanocytes. acta poloniae pharmaceutica-drug research, july-august 2016, 73(4):903-911.
[2] dong xw,jia y,lu sx,zhou x,cohen-williams m,hodgson r,li h,priestley t. the antipsychotic drug, fluphenazine, effectively reverses mechanical allodynia in rat models of neuropathic pain. psychopharmacology (berl). 2008 jan;195(4):559-68.

FLUPHENAZINE HYDROCHLORIDE Preparation Products And Raw materials

Global( 202)Suppliers
Supplier Tel Email Country ProdList Advantage
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9348 55
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
Hubei Ipure Biology Co., Ltd
+8613367258412 ada@ipurechemical.com China 10326 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671 sales@tnjchem.com China 34572 58
HONG KONG IPURE BIOLOGY CO.,LIMITED
86 18062405514 18062405514 ada@ipurechemical.com CHINA 3465 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226 sales@hzclap.com CHINA 6313 58
Xi'an MC Biotech, Co., Ltd.
029-89275612 +8618991951683 mcbio_sales@163.com China 2255 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29271 58
AFINE CHEMICALS LIMITED
0571-85134551 info@afinechem.com CHINA 15377 58

View Lastest Price from FLUPHENAZINE HYDROCHLORIDE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Fluphenazine DiHCl pictures 2023-06-07 Fluphenazine DiHCl
146-56-5
US $150.00 / kg 1kg 99.9% 10000MT Henan Bao Enluo International TradeCo.,LTD
FLUPHENAZINE HYDROCHLORIDE USP/EP/BP pictures 2021-07-24 FLUPHENAZINE HYDROCHLORIDE USP/EP/BP
146-56-5
US $1.10 / g 1g 99.9% 100 Tons min Dideu Industries Group Limited
FLUPHENAZINE HYDROCHLORIDE pictures 2020-01-18 FLUPHENAZINE HYDROCHLORIDE
146-56-5
US $3.00 / KG 1KG 98% 1kg , 5kg, 50kg Career Henan Chemical Co
  • Fluphenazine DiHCl pictures
  • Fluphenazine DiHCl
    146-56-5
  • US $150.00 / kg
  • 99.9%
  • Henan Bao Enluo International TradeCo.,LTD

FLUPHENAZINE HYDROCHLORIDE Spectrum

10-(3-(4-(2-hydroxyethyl)piperazinyl)propyl)-2-trifluoromethylphenothiazine 4-(3-(2-(trifluoromethyl)phenothiazin-10-yl)propyl)-1-piperazineethanodihy 4-(3-(2-(trifluoromethyl)phenothiazin-10-yl)propyl)-1-piperazineethanol,dihy 4-[3[2-(trifluoromethyl)-10h-phenothiazin-10-yl]propyl]-1-piperazineethano a4077 flufenazin liogen lyorodin mirenil moditen omca permitilhydrochloride squibb4918 tensofin 2-(4-(3-(2-(trifluoroMethyl)-10H-phenothiazin-10-yl)propyl)piperazin-1-yl)ethanol dihydrochloride Siqualone 1-Piperazineethanol,4-[3-[2-(trifluoroMethyl)-10H-phenothiazin-10-yl]propyl]-, hydrochloride (1:2) Fluphenazine DiHCl 4-[3-[2-(TRIFLUOROMETHYL)-10H-PHENO-THIAZIN-10-YL]-1-PIPERAZINEETHANOL 2HCL 4-[3-[2-(TRIFLUOROMETHYL)-10H-PHENOTHIAZIN-10-YL]PROPYL]-1-PIPERAZINEETHANOL DIHYDROCHLORIDE FLUPHENAZINE HYDROCHLORIDE 4-[3-[2-(Trifluoromethyl)phenothiazin-10-yl]propyl]-1- piperazineethanol Dihydrochloride Tensofi 1-Piperazineethanol, 4-3-2-(trifluoromethyl)-10H-phenothiazin-10-ylpropyl-, dihydrochloride FLUPHENAZINE HYDROCHLORIDE USP trancin Fluphenazine Hydrochloride (125 mg) Fluphenazine·dihydrochloric acid 2-[4-[3-[2-(trifluoromethyl)phenothiazin-10-yl]propyl]piperazin-1-yl]ethanol,dihydrochloride 2-(4-(3-(2-(Trifluoromethyl)-10H-phenothiazin-10-yl)propyl)piperazin-1-yl)ethan-1-ol dihydrochloride Fluphenazine Hydrochoride Fluphenazine impurity mixture CRS Fluphenazine dihydrochloride CRS Fluphenazine DiHCl (Fluphenazine Decanoate EP Impurity B DiHCl) uphenazine dihydrochL Fluphenazine Enantate EP Impurity B FLUPHENAZINE HYDROCHLORIDE USP/EP/BP Fluphenazine dihydrochloride (F0280000) Fluphenazine Hydrochloride (1282004) anatensol prolixin Prolinate FLUPHENAZINE HCL FLUPHENAZINE DIHYDROCHLORIDE 146-56-5 C22H27ClF3N3OS C22H28Cl2F3N3OS C22H28F3N3OSCl2 C22H26F3N3OS2HCl EULEXIN Heterocyclic Compounds Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Sulfur & Selenium Compounds Active Pharmaceutical Ingredients Organics