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Imipramine

Base Information Edit
  • Chemical Name:Imipramine
  • CAS No.:50-49-7
  • Molecular Formula:C19H24 N2
  • Molecular Weight:280.413
  • Hs Code.:2933990090
  • European Community (EC) Number:200-042-1
  • NSC Number:169866
  • UNII:OGG85SX4E4
  • DSSTox Substance ID:DTXSID1043881
  • Nikkaji Number:J8.587A
  • Wikipedia:Imipramine
  • Wikidata:Q58396
  • NCI Thesaurus Code:C62039
  • RXCUI:5691
  • Pharos Ligand ID:VV2MJKQ7KH9F
  • Metabolomics Workbench ID:37887
  • ChEMBL ID:CHEMBL11
  • Mol file:50-49-7.mol
Imipramine

Synonyms:4,4'-Methylenebis(3-hydroxy-2-naphthoic acid)-3-(10,11-dihydro-5H-dibenzo(b,f)azepin-5-yl)-N,N-dimethyl-1-propanamine (1:2);Imidobenzyle;Imipramine;Imipramine Hydrochloride;Imipramine Monohydrochloride;Imipramine Pamoate;Imizin;Janimine;Melipramine;Norchlorimipramine;Pryleugan;Tofranil

Suppliers and Price of Imipramine
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
  • Imipramine
  • 500ul
  • $ 306.00
  • Matrix Scientific
  • 3-(10,11-Dihydro-5H-dibenzo[b,f]azepin-5-yl)-N,N-dimethylpropan-1-amine 95+%
  • 1g
  • $ 240.00
  • Matrix Scientific
  • 3-(10,11-Dihydro-5H-dibenzo[b,f]azepin-5-yl)-N,N-dimethylpropan-1-amine 95+%
  • 5g
  • $ 819.00
  • Crysdot
  • 3-(10,11-Dihydro-5H-dibenzo[b,f]azepin-5-yl)-N,N-dimethylpropan-1-amine 95+%
  • 10g
  • $ 458.00
  • Chemtos
  • Imipraminelabeledd4Hydrochloride
  • 10 mg
  • $ 1100.00
  • Chemtos
  • Imipramine-d4HCl0.1mg/ml
  • 1ml of 0.1 mg
  • $ 50.00
  • American Custom Chemicals Corporation
  • IMIPRAMINE 95.00%
  • 1G
  • $ 255.15
  • Alichem
  • 3-(10,11-Dihydro-5H-dibenzo[b,f]azepin-5-yl)-N,N-dimethylpropan-1-amine
  • 5g
  • $ 400.00
Total 60 raw suppliers
Chemical Property of Imipramine Edit
Chemical Property:
  • Vapor Pressure:1.04E-06mmHg at 25°C 
  • Melting Point:174°C 
  • Refractive Index:1.5640 (estimate) 
  • Boiling Point:403.1°Cat760mmHg 
  • PKA:pKa 9.66(H2O,t = 25,I=0.025) (Uncertain) 
  • Flash Point:179.7°C 
  • PSA:6.48000 
  • Density:1.041g/cm3 
  • LogP:3.94000 
  • Water Solubility.:18.23mg/L(24 oC) 
  • XLogP3:4.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:280.193948774
  • Heavy Atom Count:21
  • Complexity:291
Purity/Quality:

98% *data from raw suppliers

Imipramine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Drug Classes:Antidepressant Agents
  • Canonical SMILES:CN(C)CCCN1C2=CC=CC=C2CCC3=CC=CC=C31
  • Recent ClinicalTrials:Therapeutic Efficacy in Women With Stress Urinary Incontinence
  • Recent EU Clinical Trials:Histological and clinical effects of Imipramine in the treatment of patients with cancer over-expressing Fascin1.
  • Uses Imipramine is used in depression of various etiology accompanied by motor clumsiness and enuresis in children and Parkinson’s disease. antidepressant
  • Therapeutic Function Antidepressant
  • Clinical Use Imipramine is a 10,11-dihydrodibenzazepine tertiary amine TCA that is marketed as hydrochloride and pamoate salts, both of which are administered orally. Although the hydrochloride salt may be administered in divided daily doses, imipramine's long duration of action suggests that the entire oral daily dose may be administered at one time.On the other hand, imipramine pamoate usually is administered as a single daily oral dose.
Technology Process of Imipramine

There total 17 articles about Imipramine 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 tetrahydroborate; In water; at 50 - 60 ℃; chemoselective reaction;
DOI:10.1016/j.tetlet.2010.08.045
Guidance literature:
With hydrogen; In octane; at 150 ℃; for 30h; Autoclave;
DOI:10.1039/c4cc05119j
Guidance literature:
With lithium aluminium tetrahydride; In tetrahydrofuran; for 0.5h; Heating;
DOI:10.1016/S0040-4039(00)98209-1
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