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Piperacillin Sodium Antibiotics chemical

Cat.No.S4222

Piperacillin (CL227193,Pipracil) is a semisynthetic, broad-spectrum, ampicillin derived ureidopenicillin antibiotic proposed for pseudomonas infections.
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Quality Control

Batch: Purity: 99.04%
99.04

Solubility

In vitro
Batch:

DMSO : 100 mg/mL (185.34 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : 100 mg/mL

Ethanol : 100 mg/mL

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Mass Concentration Volume Molecular Weight
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In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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%
% Tween 80
% ddH2O
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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Chemical Information, Storage & Stability

Molecular Weight 539.54 Formula

C23H27N5O7S.Na

Storage (From the date of receipt)
CAS No. 59703-84-3 Download SDF Storage of Stock Solutions

Synonyms CL227193,Pipracil SMILES CCN1CCN(C(=O)C1=O)C(=O)NC(C2=CC=CC=C2)C(=O)NC3C4N(C3=O)C(C(S4)(C)C)C(=O)[O-].[Na+]

Read more about storage stability stock solution CAS number SMILES

Mechanism of Action

Targets/IC50/Ki
beta-lactamase
In vitro

Piperacillin is a penicillin beta-lactam antibiotic used in the treatment of bacterial infections caused by susceptible, usually gram-positive, organisms. The name "penicillin" can either refer to several variants of penicillin available, or to the group of antibiotics derived from the penicillins. Piperacillin has in vitro activity against gram-positive and gram-negative aerobic and anaerobic bacteria. The bactericidal activity of Piperacillin results from the inhibition of cell wall synthesis and is mediated through Piperacillin binding to penicillin binding proteins (PBPs). By binding to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, Piperacillin inhibits the third and last stage of bacterial cell wall synthesis. Cell lysis is then mediated by bacterial cell wall autolytic enzymes such as autolysins. Piperacillin is stable against hydrolysis by a variety of beta-lactamases, including penicillinases, and cephalosporinases and extended spectrum beta-lactamases.

References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2026-08-12)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT07759453 NOT_YET_RECRUITING
Liver Transplant; Carbapenem-resistant Enterobacterales; CRE Colonization
IRCCS Azienda Ospedaliero-Universitaria di Bologna
2026-10-01 PHASE3
NCT06954129 RECRUITING
Acute Kidney Injury
University of Pennsylvania
2026-01-28 PHASE4
NCT07620223 RECRUITING
Hepatobiliary Surgery; Prophylactic Antibiotics
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
2026-05-24
NCT06123169 NOT_YET_RECRUITING
Pancreaticoduodenectomy; Antibiotherapy
University Hospital, Rouen
2026-07 PHASE3
NCT06184659 RECRUITING
Sepsis; Septic Shock
Scandinavian Critical Care Trials Group
2025-06-26 PHASE4
NCT07556107 RECRUITING
Infection; Acute Kidney Injury; Sepsis
Bassett Healthcare
2026-08-17 PHASE4

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