Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Azaperone

Base Information Edit
  • Chemical Name:Azaperone
  • CAS No.:1649-18-9
  • Molecular Formula:C19H22FN3O
  • Molecular Weight:327.402
  • Hs Code.:29335990
  • European Community (EC) Number:216-715-8
  • NSC Number:758969,170976
  • UNII:19BV78AK7W
  • DSSTox Substance ID:DTXSID2045361
  • Nikkaji Number:J7.544B
  • Wikipedia:Azaperone
  • Wikidata:Q4832244
  • NCI Thesaurus Code:C74187
  • Pharos Ligand ID:A4TVW48RQ9L3
  • Metabolomics Workbench ID:144680
  • ChEMBL ID:CHEMBL340211
  • Mol file:1649-18-9.mol
Azaperone

Synonyms:Azaperone;R-1929;R1929;Stresnil

Suppliers and Price of Azaperone
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Azaperone
  • 500ul
  • $ 523.00
  • TRC
  • Azaperone(1.0mg/mLinMethanol)
  • 5x1ml
  • $ 185.00
  • Sigma-Aldrich
  • Azaperone VETRANAL
  • 100mg
  • $ 367.00
  • Sigma-Aldrich
  • Azaperone United States Pharmacopeia (USP) Reference Standard
  • 200mg
  • $ 350.00
  • Sigma-Aldrich
  • Azaperone European Pharmacopoeia (EP) Reference Standard
  • $ 190.00
  • Sigma-Aldrich
  • Azaperone European Pharmacopoeia (EP) Reference Standard
  • y0000029
  • $ 190.00
  • DC Chemicals
  • Azaperone >98%
  • 1 g
  • $ 300.00
  • CSNpharm
  • Azaperone
  • 100mg
  • $ 77.00
  • Crysdot
  • Azaperone 98+%
  • 100mg
  • $ 107.00
  • ChemScene
  • Azaperone 99.77%
  • 500mg
  • $ 192.00
Total 102 raw suppliers
Chemical Property of Azaperone Edit
Chemical Property:
  • Appearance/Colour:Off-white solid 
  • Vapor Pressure:4.14E-10mmHg at 25°C 
  • Melting Point:87-89 °C 
  • Refractive Index:1.568 
  • Boiling Point:499.46 °C at 760 mmHg 
  • PKA:8.43±0.19(Predicted) 
  • Flash Point:255.864 °C 
  • PSA:36.44000 
  • Density:1.168 g/cm3 
  • LogP:3.00870 
  • Storage Temp.:0-6°C 
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:6
  • Exact Mass:327.17469050
  • Heavy Atom Count:24
  • Complexity:390
Purity/Quality:

99.9% *data from raw suppliers

Azaperone *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn 
  • Hazard Codes:Xn 
  • Statements: 22 
  • Safety Statements: 3/14 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Other Uses -> Pharmaceuticals
  • Canonical SMILES:C1CN(CCN1CCCC(=O)C2=CC=C(C=C2)F)C3=CC=CC=N3
  • Recent ClinicalTrials:Premedication With Melatonin and Alprazolam Combination Versus Alprazolam or Melatonin Alone
  • Description Azaperone is a sedative used in veterinary medicine to avoid mortality of pigs during transportation. This alternative substance to chlorpromazine is a sensitizer and a photosensitizer.
  • Physical properties A butyrophenone neuroleptic, azaperone occurs as a white to yellowish-white macrocrystalline powder with a melting point between 90-95°C. It is practically insoluble in water; 1 gram is soluble in 29 mL of alcohol. Azaperone may also be known as azaperonum, R-1929, Stresnil?, or Suicalm?.
  • Uses Sedative; tranquilizer. H1 antihistamine (nonsedating); leucotriene synthesis blocker
  • Indications Azaperone is officially indicated for the "control of aggressiveness when mixing or regrouping weanling or feeder pigs weighing up to 36.4 kg" (Package Insert, Stresnil?—P/M; Mallinckrodt). It is also used clinically as a general tranquilizer for swine, to allow piglets to be accepted by aggressive sows, and as a preoperative agent prior to general anesthesia or cesarean section with local anesthesia. Azaperone has been used as a neuroleptic in horses, but some horses develop adverse reactions (sweating, muscle tremors, panic reaction, CNS excitement) and IV administration has resulted in significant arterial hypotension. Because of these effects, most clinicians avoid the use of this drug in equines.
  • Therapeutic Function Neuroleptic, Hypnotic
Technology Process of Azaperone

There total 3 articles about Azaperone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium hydrogencarbonate; potassium iodide; In toluene; at 100 ℃; for 36h;
DOI:10.1021/acs.joc.9b02323
Guidance literature:
Multi-step reaction with 2 steps
1: manganese; di-tert-butyl peroxide; α,α,α-trifluorotoluene / 48 h / 100 °C / Inert atmosphere
2: potassium iodide; sodium hydrogencarbonate / toluene / 36 h / 100 °C
With manganese; di-tert-butyl peroxide; α,α,α-trifluorotoluene; sodium hydrogencarbonate; potassium iodide; In toluene;
DOI:10.1021/acs.joc.9b02323

Reference yield:

Guidance literature:
γ-Chlor-4-fluorbutyrophenon, 1-(2-Pyridyl)-piperazin (115grad);
Post RFQ for Price