Product Name

  • Name

    PROPERICYAZINE

  • EINECS
  • CAS No. 2622-26-6
  • Article Data4
  • CAS DataBase
  • Density 1.32g/cm3
  • Solubility 38.01mg/L(37 oC)
  • Melting Point 116-117°
  • Formula C21H23 N3 O S
  • Boiling Point 593.4°Cat760mmHg
  • Molecular Weight 365.499
  • Flash Point 312.7°C
  • Transport Information
  • Appearance
  • Safety Poison by ingestion, intraperitoneal, intravenous, and subcutaneous routes. Used as an antipsychotic agent. When heated to decomposition it emits very toxic fumes of CN, NOx, and SOx. See also NITRILES.
  • Risk Codes 22-36/37/38-20/21/22
  • Molecular Structure Molecular Structure of 2622-26-6 (PROPERICYAZINE)
  • Hazard Symbols
  • Synonyms Phenothiazine-2-carbonitrile,10-[3-(4-hydroxypiperidino)propyl]- (6CI,7CI,8CI); 10-[3-(4-Hydroxypiperidino)propyl]phenothiazine-2-carbonitrile;2-Cyano-10-[3-(4-hydroxy-1-piperidyl)propyl]phenothiazine;2-Cyano-10-[3-(4-hydroxypiperidino)propyl]phenothiazine; Aolept; Bayer 1409; FI6145; Nelactil; Nemactil; Neulactil; Neuleptil; Periciazine; Periciazinum;Pericyazine; Properciazine; Propericiazine; Propericyazine; RP 8909; SKF 20716
  • PSA 75.80000
  • LogP 4.01068

Synthetic route

4-HYDROXYPIPERIDINE
5382-16-1

4-HYDROXYPIPERIDINE

10H-phenothiazine-2-carbonitrile
38642-74-9

10H-phenothiazine-2-carbonitrile

1,3-chlorobromopropane
109-70-6

1,3-chlorobromopropane

periciazine
2622-26-6

periciazine

Conditions
ConditionsYield
Stage #1: 10H-phenothiazine-2-carbonitrile; 1.3-chlorobromopropane With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0 - 20℃; for 7h;
Stage #2: 4-HYDROXYPIPERIDINE With triethylamine In N,N-dimethyl-formamide at 0 - 60℃; for 42h;
40%
periciazine
2622-26-6

periciazine

10-(3-(4-oxopiperidin-1-yl)propyl)-10H-phenothiazine-2-carbonitrile
96265-39-3

10-(3-(4-oxopiperidin-1-yl)propyl)-10H-phenothiazine-2-carbonitrile

Conditions
ConditionsYield
With dmap; 2-azatricyclo[3.3.1.13,7]dec-2-yloxidanyl; copper(l) chloride In acetonitrile at 20℃; for 1h; chemoselective reaction;97%
yttrium(III) nitrate
13494-98-9

yttrium(III) nitrate

periciazine
2622-26-6

periciazine

Y(3+)*2C21H23N3OS*3NO3(1-) = [Y(C21H23N3OS)2(NO3)2](NO3)

Y(3+)*2C21H23N3OS*3NO3(1-) = [Y(C21H23N3OS)2(NO3)2](NO3)

Conditions
ConditionsYield
In ethanol 15 min; pptn. washing (EtOH), drying (vac.); elem. anal.;74%
uranyl(VI) acetate dihydrate

uranyl(VI) acetate dihydrate

periciazine
2622-26-6

periciazine

UO2(CH3CO2)2(C6H4SN((CH2)3NC5H9OH)C6H3CN)(H2O)2

UO2(CH3CO2)2(C6H4SN((CH2)3NC5H9OH)C6H3CN)(H2O)2

Conditions
ConditionsYield
In water soln. refluxed for 6 h; cooling under ice-cold water for 4 d; ppt. filtered and dried in vac.; elem. anal.;50%
zirconium(IV) nitrate

zirconium(IV) nitrate

periciazine
2622-26-6

periciazine

Zr(NO3)4 (propericiazine)

Zr(NO3)4 (propericiazine)

Conditions
ConditionsYield
In sulfuric acid; water aq. H2SO4; stirring (soln. of Zr(NO3)4 in water), addn. (soln. of ligand in water, sulphuric acid), pptn., set aside (2 h); sepn. (filtration), washing (water, EtOH), drying (vac., over fused CaCl2); elem. anal.;
rhodium(III) chloride trihydrate

rhodium(III) chloride trihydrate

periciazine
2622-26-6

periciazine

rhodium (II,III) (propericiazine)2 Cl8

rhodium (II,III) (propericiazine)2 Cl8

Conditions
ConditionsYield
In ethanol addn. of ethanolic soln. of PPC to a constantly stirred ethanolic soln. of RhCl3*3H2O at room temp., pptn.; filtration, washing with ethanol and ether, drying in vac. over fused CaCl2, elem. anal.;
ruthenium(III) chloride trihydrate

ruthenium(III) chloride trihydrate

periciazine
2622-26-6

periciazine

Ru3(C6H4SN(C3H6N(C5H9OH))C6H3(CN))2Cl8

Ru3(C6H4SN(C3H6N(C5H9OH))C6H3(CN))2Cl8

Conditions
ConditionsYield
In ethanol addn. of ethanolic N-alkylphenothiazine soln. to ethanolic RuCl3*3H2O soln., stirring slowly; filtration; washing (ethanol, ether, several times); drying (anhydrous CaCl2, desiccator); elem. anal.;
sodium tungstate (VI) dihydrate
10213-10-2

sodium tungstate (VI) dihydrate

periciazine
2622-26-6

periciazine

W2O4(C6H4SN((CH2)3NC5H9OH)C6H3CN)2(H2O)2

W2O4(C6H4SN((CH2)3NC5H9OH)C6H3CN)2(H2O)2

Conditions
ConditionsYield
With HCl In water a soln. of Na2WO4*2H2O in distd. H2O was added with stirring to a soln.of PPC in distd. H2O containing few drops of 2 M HCl; the suspn. was set aside for 3 h, filtered, washed (H2O, EtOH), dried in vac. over fused CaCl2; elem. anal.;
hexaammonium heptamolybdate tetrahydrate

hexaammonium heptamolybdate tetrahydrate

periciazine
2622-26-6

periciazine

Mo2O4(C6H4SN(CH2)3NC5H9OHC6H3CN)2(H2O)2

Mo2O4(C6H4SN(CH2)3NC5H9OHC6H3CN)2(H2O)2

Conditions
ConditionsYield
In hydrogenchloride (NH4)6Mo7O24*4H2O in 2 M HCl was added to soln. of ligand in water with vigorous stirring, suspn. set aside for 2 h; suspn. filtered, washed with water, ethanol and dried in vacuo over fused CaCl2; elem. anal.;67-79

Propericiazine Chemical Properties

Empirical Formula: C21H23N3OS
Molecular Weight: 365.4918 g/mol
EINECS: 220-071-3 
Index of Refraction: 1.694
Density: 1.32 g/cm3
Flash Point: 312.7 °C
 Storage tempreture: 2-8 °C
Enthalpy of Vaporization: 93.04 kJ/mol
Boiling Point: 593.4 °C at 760 mmHg
Vapour Pressure: 6.29E-15 mmHg at 25 °C
Structure of Propericiazine (CAS NO.2622-26-6):
           
IUPAC Name of Propericiazine (CAS NO.2622-26-6): 10-[3-(4-Hydroxypiperidin-1-yl)propyl]phenothiazine-2-carbonitrile

Propericiazine Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
bird - wild LD50 oral 100mg/kg (100mg/kg)   Toxicology and Applied Pharmacology. Vol. 21, Pg. 315, 1972.
mouse LD50 intraperitoneal 115mg/kg (115mg/kg)   Comptes Rendus des Seances de la Societe de Biologie et de Ses Filiales. Vol. 157, Pg. 1242, 1963.
mouse LD50 intravenous 27700ug/kg (27.7mg/kg)   Oyo Yakuri. Pharmacometrics. Vol. 1, Pg. 74, 1967.
mouse LD50 oral 530mg/kg (530mg/kg)   Comptes Rendus des Seances de la Societe de Biologie et de Ses Filiales. Vol. 157, Pg. 1242, 1963.
mouse LD50 subcutaneous 375mg/kg (375mg/kg)   Comptes Rendus des Seances de la Societe de Biologie et de Ses Filiales. Vol. 157, Pg. 1242, 1963.
rat LD50 intraperitoneal 85mg/kg (85mg/kg)   "Psychotropic Drugs and Related Compounds," 2nd ed., Usdin, E., and D.H. Efron, Washington, DC, 1972Vol. -, Pg. 43, 1972.
rat LD50 intravenous 35mg/kg (35mg/kg)   "Psychotropic Drugs and Related Compounds," 2nd ed., Usdin, E., and D.H. Efron, Washington, DC, 1972Vol. -, Pg. 43, 1972.
rat LD50 oral 395mg/kg (395mg/kg)   Toxicology and Applied Pharmacology. Vol. 21, Pg. 315, 1972.
rat LD50 subcutaneous 1200mg/kg (1200mg/kg)   "Psychotropic Drugs and Related Compounds," 2nd ed., Usdin, E., and D.H. Efron, Washington, DC, 1972Vol. -, Pg. 43, 1972.

Propericiazine Consensus Reports

Cyanide and its compounds are on the Community Right-To-Know List.

Propericiazine Safety Profile

Poison by ingestion, intraperitoneal, intravenous, and subcutaneous routes. Used as an antipsychotic agent. When heated to decomposition it emits very toxic fumes of CN, NOx, and SOx. See also NITRILES.
Hazard Codes of Propericiazine (CAS NO.2622-26-6): HarmfulXn
Risk Statements: 22-36/37/38-20/21/22 
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed. 
R22:Harmful if swallowed. 
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 26-36 
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. 
S36:Wear suitable protective clothing.

Propericiazine Specification

 Propericiazine ,its cas register number is 2622-26-6. It also can be called Neuleptil ; Aolept ; periciazine ; and 2-Cyano-10-[3-(4-hydroxypiperidino)propyl]phenothiazine .

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