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PIPAMPERONE DIHYDROCHLORIDE APPROX. 99

CAS No.
1893-33-0
Chemical Name:
PIPAMPERONE DIHYDROCHLORIDE APPROX. 99
Synonyms
FPA;R 3345;D02622;Propitan;Dipiperon;Dipiperal;piperonil;Piperonyl;Dipiperone;MCN-JR-3345
CBNumber:
CB5497461
Molecular Formula:
C21H30FN3O2
Molecular Weight:
375.48
MDL Number:
MFCD00242979
MOL File:
1893-33-0.mol
MSDS File:
SDS
Last updated:2024-11-19 23:02:33

PIPAMPERONE DIHYDROCHLORIDE APPROX. 99 Properties

Melting point 126°C(lit.)
Boiling point 563.7±50.0 °C(Predicted)
Density 1.1017 (estimate)
storage temp. Store at -20°C
solubility H2O: ~50 mg/mL
pka 16.20±0.20(Predicted)
form powder
color white
Water Solubility 81.7mg/L at 25℃
Merck 14,7455
LogP 2.42
EWG's Food Scores 1
FDA UNII 5402501F0W
EPA Substance Registry System Pipamperone (1893-33-0)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS09,GHS06
Signal word  Danger
Hazard statements  H301-H411
Precautionary statements  P264-P270-P301+P310-P321-P330-P405-P501
Hazard Codes  Xn
Risk Statements  22
RIDADR  UN 2811 6.1/PG III
WGK Germany  1
RTECS  DW1060000
HS Code  2933.39.3100
HazardClass  6.1
PackingGroup  III
NFPA 704
0
3 0

PIPAMPERONE DIHYDROCHLORIDE APPROX. 99 price More Price(7)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical P2315 Pipamperone >98.0%(HPLC) 1893-33-0 25mg $166 2024-03-01 Buy
TCI Chemical P2315 Pipamperone >98.0%(HPLC) 1893-33-0 100mg $496 2024-03-01 Buy
Chem-Impex 38191 Pipamperone,98%(HPLC) 98%(HPLC) 1893-33-0 25MG $146.72 2021-12-16 Buy
ChemScene CS-0020023 Pipamperone 99.89% 1893-33-0 5mg $150 2021-12-16 Buy
AK Scientific 0155BA Pipamperone 1893-33-0 25mg $263 2021-12-16 Buy
Product number Packaging Price Buy
P2315 25mg $166 Buy
P2315 100mg $496 Buy
38191 25MG $146.72 Buy
CS-0020023 5mg $150 Buy
0155BA 25mg $263 Buy

PIPAMPERONE DIHYDROCHLORIDE APPROX. 99 Chemical Properties,Uses,Production

Originator

Dipiperon ,Janssen, W. Germany ,1961

Uses

Antipsychotic.

Definition

ChEBI: A member of the class of bipiperidines that is 1,4'-bipiperidine which is substituted at the 1' and 4' positions by 4-(p-fluorophenyl)-4-oxobutyl and carboxamide groups, respectively. A first generation antipsychotic, its properties are gener lly similar to those of haloperidol.

Manufacturing Process

To a stirred solution of 130.4 parts of potassium cyanide and 243.2 parts of piperidine hydrochloride in a mixture of 800 parts of water and 320 parts of ethanol is added portionwise 378 parts of 1-benzyl-4-piperidone. After about one hour a solid starts to precipitate. Stirring is continued for 24 hours. The reaction mixture is filtered and the solid is recrystallized from 1,200 parts of diisopropyl ether. On cooling to room temperature a first crop of 1-benzyl-4cyano-4-piperidinopiperidine melting at about 104°C to 106°C is obtained. By concentrating and further cooling of the mother liquor a second crop of the above compound is obtained.
A mixture of 14.1 parts of 1-benzyl-4-cyano-4-piperidinopiperidine and 40 parts of 90% sulfuric acid is heated on a steam bath for 10 minutes. Without further heating, the mixture is stirred until a temperature of about 20°C is obtained. The mixture is then poured into 150 parts of ice-water and the resultant solution is alkalized with excess ammonium hydroxide solution. The aqueous solution is decanted from the precipitated oil. On treating this oil with 80 parts of acetone, crystallization sets in. After one hour the solid is filtered off and dried to yield 1-benzyl-4-piperidinopiperidine-4-carboxamide melting at about 137.5°C to 140°C.
A mixture of 215 parts of 1-benzyl-4-piperidinopiperidine-4-carboxamide, 1,200 parts of isopropyl alcohol, 1,000 parts of distilled water and 157 parts of hydrogen chloride is debenzylated under atmospheric pressure and at a temperature of about 40°C in the presence of 40 parts of a 10% palladiumon-charcoal catalyst. After the calculated amount of hydrogen is taken up, hydrogenation is stopped. The mixture is filtered and the filtrate is evaporated. The semisolid residue is treated with a mixture of 80 parts of acetone and 80 parts of benzene and evaporated again. The residue is triturated in 200 parts of methanol and filtered, yielding the dihydrochloride of 4-piperidinopiperidine-4-carboxamide melting at about 299°C to 300.8°C with decomposition. A sample of 20 parts of the dihydrochloride is dissolved in 30 parts of water. The aqueous solution is alkalized with 15 parts of 44% sodium hydroxide and stirred for a short time. The solid obtained is filtered off yielding crude product. To separate the free base from organic and inorganic salts, it is extracted overnight in a Soxhlet apparatus with toluene. The toluene extract is evaporated and the solid residue is filtered off, yielding 4piperidinopiperidine-4-carboxamide melting at about 118.5°C to 119.5°C.
To a mixture of 4.1 parts of 4-piperidinopiperidine-4-carboxamide, 6.4 parts of sodium carbonate, and a few crystals of potassium iodide in 100 parts of anhydrous toluene is added dropwise a solution of 5.6 parts of γ-chloro-4fluorobutyrophenone and 40 parts of anhydrous toluene at a temperature of 30°C to 40°C. The mixture is stirred and refluxed for 48 hours. The reaction mixture is cooled and divided between 50 parts of water and 60 parts of chloroform. The combined organic layers - toluene and chloroform - are dried over potassium carbonate, filtered, and evaporated. The oily residue solidifies on treatment with 80 parts of ether. After cooling for 30 minutes at 0°C, there is obtained 1-[γ-(4-fluorobenzoyl)propyl]-4-piperidinopiperidine-4-carboxamide melting at about 124.5°C to 126°C.

brand name

[Name previously used: Floropipamide.].

Therapeutic Function

Antipsychotic

Safety Profile

Poison by ingestion, subcutaneous, and intravenous routes. An experimental teratogen. When heated to decomposition it emits very toxic fumes of Fand Nox.

PIPAMPERONE DIHYDROCHLORIDE APPROX. 99 Preparation Products And Raw materials

PIPAMPERONE DIHYDROCHLORIDE APPROX. 99 Suppliers

Global( 46)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 32165 58
Career Henan Chemica Co
+86-0371-86658258 +8613203830695 laboratory@coreychem.com China 30240 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763 sales@tnjchem.com China 34563 58
AFINE CHEMICALS LIMITED
+86-0571-85134551 sales@afinechem.com China 15352 58
Baoji Guokang Bio-Technology Co., Ltd.
0917-3909592 13892490616 gksales1@gk-bio.com China 9314 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com China 52849 58
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923 1026@dideu.com China 8670 58
TargetMol Chemicals Inc.
support@targetmol.com United States 38632 58
GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 49978 58
Shanghai Acmec Biochemical Technology Co., Ltd.
+undefined18621343501 product@acmec-e.com China 33338 58

View Lastest Price from PIPAMPERONE DIHYDROCHLORIDE APPROX. 99 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Pipamperone pictures 2024-11-19 Pipamperone
1893-33-0
US $56.00-122.00 / mg 99.94% 10g TargetMol Chemicals Inc.
Pipamperone pictures 2024-11-19 Pipamperone
1893-33-0
US $56.00-122.00 / mg 99.94% 10g TargetMol Chemicals Inc.
Piperonyl butoxide pictures 2021-07-10 Piperonyl butoxide
1893-33-0
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
  • Pipamperone pictures
  • Pipamperone
    1893-33-0
  • US $56.00-122.00 / mg
  • 99.94%
  • TargetMol Chemicals Inc.
  • Pipamperone pictures
  • Pipamperone
    1893-33-0
  • US $56.00-122.00 / mg
  • 99.94%
  • TargetMol Chemicals Inc.
  • Piperonyl butoxide pictures
  • Piperonyl butoxide
    1893-33-0
  • US $15.00-10.00 / KG
  • 99%+ HPLC
  • Zhuozhou Wenxi import and Export Co., Ltd
4'-Fluoro-4-(4-N-piperidino-4-carbamidopiperidino)butyrophenone Dipiperal Dipiperon Dipiperone Floropipamide FPA Isonipecotamide, 1-(3-(p-fluorobenzoyl)propyl)-4-piperidino- MCN-JR-3345 p-Fluoro-gamma-(4-piperidino-4-carbamoylpiperidino)butyrophenone Pipaneperone piperonil Piperonyl Propitan R 3345 PIPAMPERONE DIHYDROCHLORIDE APPROX. 99 (1,4'-Bipiperidine)-4'-carboxamide, 1'-(3-(p-fluorobenzoyl)propyl)- D02622 Pipamperone (usan/inn) -[3-(p-fluorobenzoyl)propyl]- (7CI,8CI) -Bipiperidine]-4 -carboxaMide,1 PIPAMPERONE DIHYDROCHLORIDE APPROX [1,4'-Bipiperidine]-4'-carboxamide, 1'-[4-(4-fluorophenyl)-4-oxobutyl]- 1'-(3-(p-Fluorobenzoyl)propyl)(1,4'-bipiperidine)-4'-carboxamide 1-(3-(p-fluorobenzoyl)propyl)-4-piperidino-isonipacotamid 1’-(3-(p-fluorobenzoyl)propyl)(1,4’-bipiperidine)-4’-carboxamide 4’-bipiperidine)-4’-carboxamide,1’-(3-(p-fluorobenzoyl)propyl)-( 4’-bipiperidine)-4’-carboxamide,1’-(4-(4-fluorophenyl)-4-oxobutyl)-( 4’-fluoro-4-(4-n-piperidino-4-carbamidopiperidino)butyrophenone 1'-[4-(4-Fluorophenyl)-4-oxobutyl]-[1,4'-bipiperidine]-4'-carboxamide PIPAMPERONE HCL R-3345,Pipamperone,R3345,5-HT Receptor,Serotonin Receptor,inhibit,Dopamine Receptor,Inhibitor,5-hydroxytryptamine Receptor (3RS)-9,10-difluoro-3-methyl-7-oxo-2,3-dihydro-7h-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylicacid(fPa), 1893-33-0 C21H30FN3O2