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| Product | Description | |
|---|---|---|
| Ampicillin sodium | Ampicillin is a beta-lactam antibiotic that is a part of the aminopenicillin family. It is mainly used for infections and sepsis of the lungs, intestines, biliary tract, urinary tract caused by sensitive bacteria. Synonyms: D-(-)-6-(2-Amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Monosodium Salt; [2S-[2α,5α,6β(S*)]]-6-[(Aminophenylacetyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Monosodium Salt; (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; Alpen N; Amcill S; Ampi-Dry 5000; Ampicillin Sodium; Ampicillin Sodium Salt; Ampicillin-Na; Ampicin; Anhypen; Binotal Sodium; Britapen Injection; Cilleral; D-α-Aminobenzylpenicillin Sodium Salt; Monosodium Ampicillin; Omnipen N; Pamecil; Pen A/N; Penbritin S; Pentrex; Polycillin N; Principen N; Sodium 6-(2-Amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate; Benzylpenicillin Sodium; Amcill-S; Ampicillin natrium. Grade: 97%. CAS No. 69-52-3. Molecular formula: C16H18N3NaO4S. Mole weight: 371.39. |  |
| Ampicillin sodium | Ampicillin sodium (D-(-)-α-Aminobenzylpenicillin sodium salt) is a broad-spectrum beta-lactam antibiotic against a variety of gram-positive and gram-negative bacteria [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: D-(-)-α-Aminobenzylpenicillin sodium salt. CAS No. 69-52-3. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0522A. |  |
| 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. |  |
| Ampicillin Sodium | Ampicillin Sodium - Agriculture Chemicals. SUPPLIERS TO BUSINESS CUSTOMERS ONLY. |  North America & APAC |
| Ampicillin Sodium | Ampicillin Sodium. Grades: USP. CAS No. 69-52-3. Product ID: 8-01655. Molecular formula: C16H18N3NaO4S. Mole weight: 371.39. Properties: |  |
| Ampicillin Sodium | Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmacopeia & metrological institutes standards. | |
| Ampicillin Sodium Mixture With Sulbactam Sodium | Ampicillin Sodium Mixture with Sulbactam Sodium is a β-lactamase inhibitor used to enhance the effectiveness of β-lactam antibiotics. Synonyms: Unacyne; Unacid; Unasyn-S; Yucion-S. CAS No. 117060-71-6. Molecular formula: C25H29N3Na2O9S2. Mole weight: 625.62. | |
| Ampicillin sodium salt | 100g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H18N3NaO4S. CAS No. 69-52-3. Prepack ID 23337642-100g. Molecular Weight 371.39. See USA prepack pricing. |  |
| Ampicillin sodium salt | 25g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H18N3NaO4S. CAS No. 69-52-3. Prepack ID 23337642-25g. Molecular Weight 371.39. See USA prepack pricing. | |
| Ampicillin sodium salt | powder or crystals, BioReagent, suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| Ampicillin Sodium Salt | Ampicillin Sodium Salt is a readily-soluble form of ampicillin. It belongs to the group of beta-lactam antibiotics. These antibotics gram-negative bacteria to which E. coli and Salmonella belong. beta-lactam antibiotic prevent the formation of peptidoglycan, an essential building block of the cell membrane. Thus, preventing growth of cells. Used to select for drug-resistant, plasmid-bearing bacteria. Group: Biochemicals. Alternative Names: 6-[D-(-)-alpha-Aminophenylacetamido]-penicillanic acid, sodium salt; Sodium [2S-[2α,5α,6 β (S*)]]-6-(aminophenylacetamido)-3, 3-dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylate. Grades: Molecular Biology Grade. CAS No. 69-52-3. Pack Sizes: 5g, 25g, 100g, 250g, 500g. Molecular Formula: C16H18N3O4SNa, Molecular Weight: 371.4. US Biological Life Sciences. |  Worldwide |
| Ampicillin Diketopiperazine Sodium Salt (Mixture of Diastereomers) | Ampicillin Diketopiperazine Sodium Salt (Mixture of Diastereomers). Uses: For analytical and research use. Group: Impurity standards. Pack Sizes: 2.5MG. Catalog: APS005759. Format: Neat. Shipping: Room Temperature. | |
| Ampicillin Dimer Tri-sodium Salt (Mixture of Diastereomers) | Ampicillin Dimer Tri-sodium Salt is an impurity of Ampicillin (A634300), a β-lactam antibiotic used for treating bacterial infection. Ampicillin interferes with cell wall synthesis in bacteria. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C32H37N6Na3O9S2. 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 Solution 50mg/ml | Ampicillin Solution, 50mg/ml, is a convenient, ready to use concentrated solution for molecular biology selection applications. It belongs to the group of beta-lactam antibiotics. These antibotics gram-negative bacteria to which E. coli and Salmonella belong. Beta-lactam antibiotic prevent the formation of peptidoglycan, an essential building block of the cell membrane. Thus, preventing growth of cells. Group: Biochemicals. Alternative Names: 6-[D-(-)-alpha-Aminophenylacetamido]-penicillanic acid, sodium salt; Sodium [2S-[2α,5α,6 β (S*)]]-6-(aminophenylacetamido)-3, 3-dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylate. Grades: Molecular Biology Grade. CAS No. 69-52-3. Pack Sizes: 20ml, 5x20ml. US Biological Life Sciences. | Worldwide |
| Azidocillin | Azidocillin is produced by the strain of 6-APA and Ampicillin. The activity of anti-hemolytic Streptococcus, Streptococcus pneumoniae and enterococcus is slightly better than penicillin, while staphylococcus aureus, which is sensitive to penicillin, is slightly better than penicillin, and is less stable to penicillinase than amamicillin to influenza bacilli. Stable to acid, oral. The preparation is its sodium salt or potassium salt (melting point 194°C decomposition), used as an antibacterial agent and feed additive. Synonyms: AZIDOCILLIN; GLOBACILLIN; 6α-(2-Azido-2-phenylacetylamino)penicillanic acid; BRL 2534; SPC 297 D. Grade: 95%. CAS No. 17243-38-8. Molecular formula: C16H17N5O4S. Mole weight: 375.41. | |
| β-Lactamase Blend, Recombinant | β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. Group: Enzymes. Synonyms: β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Activity: 600-1500 IU beta-lactamase I per vial; 60-100 IU beta-lactamase II per vial. Storage: 2-8°C. Form: Lyophilized powder containing sodium chloride, potassium phosphate and sorbitol. Source: E. coli. β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Cat No: NATE-0776. |  |
| β-Lactamase from Pseudomonas aeruginosa, Recombinant | β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. Applications: Β-lactamase is used to inactivate β-lactam antibiotics by breaking open the β-lactam ring. β-lactamase is used to study antibiotic resistance and resistance suppression. product is produced from pseudomonas aeruginosa and is expressed in e. coli. Group: Enzymes. Synonyms: β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 907. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Activity: > 20 U/mg (with cephalosporin C); > 400 U/mg (with benzylpenicilin). Storage: 2-8°C. Form: Lyophilized powder containing sodium chloride and potassium phosphate. Source: E. coli. Species: Pseudomonas aeruginosa. β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Cat No: NATE-0777. | |
| Native Enterobacter cloacae β-Lactamase | β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. Protein determined by biuret. Applications: Β-lactamase is used to inactivate β-lactam antibiotics by breaking open the β-lactam ring. β-lactamase is used to study antibiotic resistance and resistance suppression1. this product is produced from enterobacter cloacae. Group: Enzymes. Synonyms: β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC . Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Activity: 6-18 units/mg protein (using benzylpenicillin); 0.2-0.6 units/mg protein (using benzylpenicillin). Storage: 2-8°C. Form: Lyophilized powder containing sodium phosphate and sodium Citrate buffer salts. Source: Enterobacter cloacae. β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Cat No: NATE-0774. | |
| Native Pseudomonas fluorescens β-Lactamase | β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. Group: Enzymes. Synonyms: β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Storage: 2-8°C. Form: Lyophilized powder containing potassium phosphate and sodium bicarbonate. Source: Pseudomonas fluorescens. β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Cat No: NATE-0775. | |
| Piperacillin sodium | 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. | |
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