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Piperacillin is a semisynthetic, broad-spectrum, ampicillin derived ureidopenicillin antibiotic proposed for pseudomonas infections. Uses: Anti-bacterial agents. Synonyms: CL227193; CL 227193; CL-227193. Grade: >98%. CAS No. 59703-84-3. Molecular formula: C23H27N5O7SNa. Mole weight: 539.54.
Piperacillin sodium
Piperacillin sodium is a semisynthetic broad-spectrum β-lactam antibiotic which exhibits potent bactericidal activity against Gram-negative bacteria as well as select Gram-positive strains through penicillin-binding proteins. Piperacillin is most commonly used in combination with the β-lactamase inhibitor Tazobactam [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Sodium piperacillin. CAS No. 59703-84-3. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1286.
Piperacillin sodium salt
analytical standard. Group: Application areas.
Piperacillin sodium salt
Piperacillin sodium salt. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g. US Biological Life Sciences.
Worldwide
Piperacillin Sodium Salt
1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C23H26N5NaO7S. CAS No. 59703-84-3. Prepack ID 26952641-1g. Molecular Weight 539.54. See USA prepack pricing.
Piperacillin Sodium Salt
5g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C23H26N5NaO7S. CAS No. 59703-84-3. Prepack ID 26952641-5g. Molecular Weight 539.54. See USA prepack pricing.
1-Benzyl-2,3-dioxopiperazine
1-Benzyl-2,3-dioxopiperazine is an intermediate used in the new process for the synthesis of Piperacillin sodium. Group: Biochemicals. Grades: Highly Purified. CAS No. 63352-56-7. Pack Sizes: 10mg, 25mg. Molecular Formula: C11H12N2O2. US Biological Life Sciences.
Worldwide
1-Benzyl-4-ethylpiperazine-2,3-dione-d5
1-Benzyl-4-ethylpiperazine-2,3-dione-d5 is an isotope labelled intermediate used in the new process for the synthesis of Piperacillin sodium. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 25mg. Molecular Formula: C13H11D5N2O2. US Biological Life Sciences.
Worldwide
1-Ethyl-2,3-dioxopiperazine
An impurity of Piperacillin, which is a broad-spectrum antibiotic used to treat serious, hospital-acquired infections in combination with the beta lactamase inhibitor tazobactam. Synonyms: Piperacillin Impurity E; Piperacillin EP Impurity E; Piperacillin Sodium Impurity E [EP]; Piperacillin Monohydrate Impurity E [EP]; N-Ethyl-2,3-dioxopiperazine; 1-Ethyl-2,3-piperazinedione; N-Ethylpiperazine-2,3-dione; 4-Ethyl-2,3-dioxopiperazine; 4-Ethyl-2,3-piperazinedione; 1-Ethyl-2,3-diketopiperazine; Piperacillin Related Compound E (USP); USP Piperacillin Related Compound E; Piperacillin USP Related Compound E. Grade: >95%. CAS No. 59702-31-7. Molecular formula: C6H10N2O2. Mole weight: 142.16.
1-Ethyl-2,3-dioxopiperazine
An intermediate used in the new process for the synthesis of Piperacillin sodium. Group: Biochemicals. Alternative Names: 1-Ethyl-2,3-piperazinedione; N-Ethylpiperazine-2,3-dione; T 1982C. Grades: Highly Purified. CAS No. 59702-31-7. Pack Sizes: 1g, 10g, 25g. US Biological Life Sciences.
Worldwide
1-Ethyl-2,3-dioxopiperazine-d5
1-Ethyl-2,3-dioxopiperazine-d5 is an isotope labelled intermediate used in the new process for the synthesis of Piperacillin sodium. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 25mg. Molecular Formula: C6H5D5N2O2. US Biological Life Sciences.
Worldwide
6-Aminopenicillanic acid
An impurity of Piperacillin, which is a broad-spectrum antibiotic used to treat serious, hospital-acquired infections in combination with the beta lactamase inhibitor tazobactam. Synonyms: Piperacillin Impurity H; Piperacillin Sodium Impurity H [EP]; Piperacillin Monohydrate Impurity H [EP]; (2S,5R,6R)-6-Amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; 6-Aminopenicillamic acid; 6-APA; Sulbactam Impurity B; Amoxicillin Impurity A; Amoxicillin Related Compound A; Amoxicillin EP Impurity A; Ampicillin EP Impurity A; Penicin; Penin; Aminopenicillanic acid; 6-Aps; Phenacyl 6-aminopenicillinate; Piperacillin EP Impurity H. Grade: >95%. CAS No. 551-16-6. Molecular formula: C8H12N2O3S. Mole weight: 216.26.
6-APA Piperacillin Dimer
An impurity of Piperacillin, which is a broad-spectrum antibiotic used to treat serious, hospital-acquired infections in combination with the beta lactamase inhibitor tazobactam. Synonyms: Piperacillin penicillamide; Piperacillin Impurity S; Piperacillin Sodium Impurity S [EP]; Piperacillin Monohydrate Impurity S [EP]; (2S,5R,6R)-6-[(2S,5R,6R)-6-[(2R)-2-(4-Ethyl-2,3-dioxopiperazine-1-carboxamido)-2-phenylacetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; [(4-Ethyl-2,3-dioxopiperazin-1-yl)carbonyl] Ampicillinamide of 6-Aminopencillanic Acid; Piperacillin EP Impurity S. Grade: 97%. Molecular formula: C31H37N7O9S2. Mole weight: 715.80.
Ampicillin
Ampicillin is a broad-spectrum antibiotic used to prevent and treat a variety of bacterial infections. It is used to treat infectious diseases caused by sensitive chicken bacteria, such as Escherichia coli, Salmonella, Pasteurella, Staphylococcus and Streptococcus infections. Synonyms: Piperacillin EP Impurity A; (2S,5R,6R)-6-[(2R)-2-Amino-2-phenylacetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; Pentrexyl; Principen; D-(-)-α-Aminobenzylpenicillin; Sultamicillin EP Impurity C; Aminobenzylpenicillin; Ampicillin acid; Amcill; Polycillin; Principen; Omnipen; Ampicilline; Penbritin; 6-[D-(-)-α-Aminophenylacetamido]penicillanic acid; D-(-)-6-(α-Aminophenylacetamido)penicillanic acid; D-(-)-α-Aminopenicillin; D-Ampicillin; Piperacillin sodium Impurity A [EP]; Piperacillin Monohydrate Impurity A [EP]. Grade: >98%. CAS No. 69-53-4. Molecular formula: C16H19N3O4S. Mole weight: 349.40.
Ampicillin sodium
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standardsimpurity standardspharmaceutical toxicologypharmacopoeial standards. Alternative Names: Ampicin, Ampicillin sodium, Monosodium ampicillin, Ampicillin Sodium, Sodium 6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate, Pentrex, [2S-[2alpha,5alpha,6beta(S*)]]-6-[(Aminophenylacetyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid monosodium salt, Sodium ampicillin, Principen N, Anhypen, Binotal sodium, D-alpha-Aminobenzylpenicillin sodium salt, Ampicillin sodium salt, D-(-)-6-(2-Amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid monosodium salt, Penbritin S, Omnipen N, Piperacillin Sodium Imp. A (EP) as Sodium Salt, Sodium binotal,Piperacillin Sodium Imp. A (EP), Sodium P-50, Polycillin N, Sodium 6-[D-alpha-aminophenylacetamido]penicillanoate, Sodium D-alpha-aminobenzylpenicillanate, Amcill S, Solampi, Alpen N, Ampicillin-Na, (2S,5R,6R)-6-[[(2R)-Aminophenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid monosodium salt, Ampi-Dry 5000, Pen A/N, Piperacillin Imp. A (EP), Sodium ampicillinate, Piperacillin Imp. A (EP) as Sodium Salt, Britapen injection, Cilleral.
Azlocillin sodium salt
Azlocillin is an acylampicillin antibiotic with an extended spectrum of activity and greater in vitro potency than the carboxy penicillins. Azlocillin is similar to mezlocillin and piperacillin. It demonstrates antibacterial activity against a broad spectrum of bacteria, including Pseudomonas aeruginosa and, in contrast to most cephalosporins, exhibits activity against enterococci. Uses: Anti-bacterial agents. Synonyms: Bayer Brand of Azlocillin; Sodium Azlocillin; Securopen; Bay-e 6905; Baye 6905; Bay e 6905; Azlocillin; Azlocillin Bayer Brand. Grade: >98%. CAS No. 37091-65-9. Molecular formula: C20H23N5O6SNa. Mole weight: 484.48.
Cefpiramide sodium
Cefpiramide sodium is a new Pseudomonas-active cephalosporin with a broad spectrum of antibacterial activity. It was more active against Acinetobacter spp. and Pseudomonas spp. It inhibited many Pseudomonas aeruginosa resistant to carbenicillin, piperacillin, and cefotaxime, but it was less active than ceftazidime and cefsulodin. It also inhibited staphylococci and streptococci and had appreciable activity against Streptococcus faecalis and Listeria moncytogenes. Uses: Anti-bacterial agents. Synonyms: SM-1652; Wy-44635; SM 1652; Wy 44635; SM1652; Wy44635. Grade: >98%. CAS No. 74849-93-7. Molecular formula: C25H23N8NaO7S2. Mole weight: 635.63.
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