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Penethamate

Base Information Edit
  • Chemical Name:Penethamate
  • CAS No.:3689-73-4
  • Molecular Formula:C22H31 N3 O4 S
  • Molecular Weight:433.572
  • Hs Code.:
  • UNII:7Y8RF01X2J
  • DSSTox Substance ID:DTXSID20190371
  • Nikkaji Number:J239.349B
  • Wikidata:Q27269015
  • ChEMBL ID:CHEMBL2110695
  • Mol file:3689-73-4.mol
Penethamate

Synonyms:benzylpenicillin-diethylaminoethyl ester hydroiodide;Leocillin;Mamyzin;penethamate;penethamate hydroiodide;penethamate hydroiodide, monohydrochloride;penethamathydrojodid;penicillin G 2-(diethylamino)ethyl ester hydroiodide

Suppliers and Price of Penethamate
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
  • American Custom Chemicals Corporation
  • PENETHAMATE 95.00%
  • 5MG
  • $ 505.19
Total 12 raw suppliers
Chemical Property of Penethamate Edit
Chemical Property:
  • Vapor Pressure:1.76E-16mmHg at 25°C 
  • Boiling Point:644.1°Cat760mmHg 
  • PKA:13.54±0.60(Predicted) 
  • Flash Point:343.3°C 
  • PSA:104.25000 
  • Density:1.24g/cm3 
  • LogP:1.99000 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:10
  • Exact Mass:433.20352765
  • Heavy Atom Count:30
  • Complexity:646
Purity/Quality:

99%, *data from raw suppliers

PENETHAMATE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCN(CC)CCOC(=O)C1C(SC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)(C)C
  • Isomeric SMILES:CCN(CC)CCOC(=O)[C@H]1C(S[C@H]2N1C(=O)[C@H]2NC(=O)CC3=CC=CC=C3)(C)C
Technology Process of Penethamate

There total 6 articles about Penethamate 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 tris(acetoxy)borohydride; In 1,2-dichloro-ethane; at 20 - 30 ℃; for 6h; Solvent;
Guidance literature:
In N,N-dimethyl-formamide; at 60 ℃; for 5h;
Guidance literature:
In N,N-dimethyl-formamide; at 60 ℃; for 5h;
Refernces Edit
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