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Isopromethazine hydrochloride

Base Information
  • Chemical Name:Isopromethazine hydrochloride
  • CAS No.:5568-90-1
  • Molecular Formula:C17H21ClN2S
  • Molecular Weight:320.88
  • Hs Code.:2934300000
  • UNII:SNR56923ZU
  • DSSTox Substance ID:DTXSID10971030
  • Wikidata:Q27289303
  • Mol file:5568-90-1.mol
Isopromethazine hydrochloride

Synonyms:Isopromethazine hydrochloride;5568-90-1;Iso Promethazine Hydrochloride;Diprazin hydrochloride;Isopromethazine HCl;N,N-dimethyl-2-phenothiazin-10-ylpropan-1-amine;hydrochloride;UNII-SNR56923ZU;SNR56923ZU;N-(beta-Dimethylamino-alpha-methylethyl)phenothiazine hydrochloride;Phenothiazine, 10-(2-(dimethylamino)-1-methylethyl)-, hydrochloride;10H-Phenothiazine-10-ethanamine, N,N,.beta.-trimethyl-, monohydrochloride;10H-Phenothiazine-10-ethanamine, N,N,beta-trimethyl-, monohydrochloride;(2RS)-N,N-Dimethyl-2-(10H-phenothiazin-10-yl)propan-1-amine Hydrochloride (Isopromethazine Hydrochloride);Phenothiazine, 10-[2-(dimethylamino)-1-methylethyl]-, monohydrochloride;PHENOTHIAZINE, 10-(2-(DIMETHYLAMINO)-1-METHYLETHYL)-, MONOHYDROCHLORIDE;SCHEMBL3712233;DTXSID10971030;10-[2-(Dimethylamino)-1-methylethyl]phenothiazine Monohydrochloride;AKOS030242437;ISOPROMETHAZINE HYDROCHLORIDE [MI];LS-105474;FT-0670482;ISOPROMETHAZINE HYDROCHLORIDE [WHO-DD];Q27289303;N,N-Dimethyl-2-(10H-phenothiazin-10-yl)propan-1-amine hydrochloride;10H-PHENOTHIAZINE-10-ETHANAMINE, N,N,.BETA.-TRIMETHYL-, HYDROCHLORIDE (1:1);N,N-Dimethyl-2-(10H-phenothiazin-10-yl)propan-1-amine--hydrogen chloride (1/1)

Suppliers and Price of Isopromethazine hydrochloride
Supply Marketing:
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
  • TRC
  • IsoPromethazineHydrochloride
  • 1g
  • $ 1695.00
  • TRC
  • IsoPromethazineHydrochloride
  • 100mg
  • $ 215.00
  • American Custom Chemicals Corporation
  • ISOPROMETHAZINE HYDROCHLORIDE 95.00%
  • 2.5G
  • $ 1815.00
  • American Custom Chemicals Corporation
  • ISOPROMETHAZINE HYDROCHLORIDE 95.00%
  • 250MG
  • $ 721.88
Total 11 raw suppliers
Chemical Property of Isopromethazine hydrochloride
Chemical Property:
  • Vapor Pressure:1.02E-06mmHg at 25°C 
  • Melting Point:204 °C 
  • Boiling Point:403.4°Cat760mmHg 
  • Flash Point:197.8°C 
  • PSA:31.78000 
  • Density:g/cm3 
  • LogP:5.10640 
  • Storage Temp.:Hygroscopic, Refrigerator, Under inert atmosphere 
  • Solubility.:Chloroform (Slightly), Methanol (Slightly), Water (Slightly, Sonicated) 
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:320.1113975
  • Heavy Atom Count:21
  • Complexity:298
Purity/Quality:

99%, *data from raw suppliers

IsoPromethazineHydrochloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(CN(C)C)N1C2=CC=CC=C2SC3=CC=CC=C31.Cl
  • Uses Promethazine (P757000) impurity. Iso Promethazine Hydrochloride (Promethazine EP Impurity B) is a Promethazine (P757000) impurity.
Technology Process of Isopromethazine hydrochloride

There total 3 articles about Isopromethazine hydrochloride 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 lithium aluminium tetrahydride; In tetrahydrofuran; for 2h;
DOI:10.1002/jps.2600720525
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) n-butyllithium / 1.) ether, hexane, -30 - -20 deg C, 30 min, 2.) 1 h
2: 72 percent / lithium aluminum hydride / tetrahydrofuran / 2 h
With lithium aluminium tetrahydride; n-butyllithium; In tetrahydrofuran;
DOI:10.1002/jps.2600720525
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) n-butyllithium / 1.) ether, hexane, -30 - -20 deg C, 30 min, 2.) 1 h
2: 72 percent / lithium aluminum hydride / tetrahydrofuran / 2 h
With lithium aluminium tetrahydride; n-butyllithium; In tetrahydrofuran;
DOI:10.1002/jps.2600720525
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