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Ticarcillin sodium

Base Information Edit
  • Chemical Name:Ticarcillin sodium
  • CAS No.:74682-62-5
  • Molecular Formula:C15H15N2NaO6S2
  • Molecular Weight:406.416
  • Hs Code.:2941106000
  • Mol file:74682-62-5.mol
Ticarcillin sodium

Synonyms:4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid, 6-[(carboxy-3-thienylacetyl)amino]-3,3-dimethyl-7-oxo-, monosodium salt,[2S-[2a,5a,6b(S*)]]-;D-Ticarcillinsodium salt;Ticarcillin monosodium;

Suppliers and Price of Ticarcillin sodium
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
  • Sigma-Aldrich
  • Ticarcillin monosodium
  • 350mg
  • $ 366.00
  • Sigma-Aldrich
  • Ticarcillin monosodium European Pharmacopoeia (EP) Reference Standard
  • y0000465
  • $ 190.00
  • Arctom
  • Ticarcillinsodium
  • 5g
  • $ 412.00
  • Arctom
  • Ticarcillinsodium
  • 1g
  • $ 118.00
Total 54 raw suppliers
Chemical Property of Ticarcillin sodium Edit
Chemical Property:
  • Vapor Pressure:7.97E-25mmHg at 25°C 
  • Boiling Point:768.3 °C at 760 mmHg 
  • Flash Point:418.4 °C 
  • PSA:183.21000 
  • LogP:-1.79260 
  • Storage Temp.:-20°C 
Purity/Quality:

98%,99%, *data from raw suppliers

Ticarcillin monosodium *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses Ticar (Glaxo-SmithKline).
  • Therapeutic Function Antibiotic
  • Clinical Use Ticarcillin disodium, α-carboxy-3-thienylpenicillin (Ticar),is an isostere of carbenicillin in which the phenyl group is replacedby a thienyl group. This semisynthetic penicillinderivative, like carbenicillin, is unstable in acid and, therefore,must be administered parenterally. It is similar tocarbenicillin in antibacterial spectrum and pharmacokineticproperties. Two advantages for ticarcillin are claimed:(a) slightly better pharmacokinetic properties, includinghigher serum levels and a longer duration of action; and(b) greater in vitro potency against several species of Gramnegativebacilli, most notably P. aeruginosa and Bacteroidesfragilis. These advantages can be crucial in the treatment ofserious infections requiring high-dose therapy.
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