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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. Grades: 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 | Ampicillin Sodium - Agriculture Chemicals. SUPPLIERS TO BUSINESS CUSTOMERS ONLY. |  North America & APAC |
| Ampicillin Sodium EP Impurity N | Ampicillin Sodium EP Impurity N. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C48H59N9O13S3. Mole Weight: 1066.23. Catalog: APB06578. |  |
| 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 | 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 |
| Ampicillin EP Impurity M Disodium Salt (Ampicillin Dimer Disodium Salt) | Ampicillin EP Impurity M Disodium Salt (Ampicillin Dimer Disodium Salt). Uses: For analytical and research use. Group: Impurity standards. Alternative Names: sodium (2S,5R,6R)-6-((2R)-2-(2-((R)-2-amino-2-phenylacetamido)-2-((4S)-4-carboxylato-5,5-dimethylthiazolidin-2-yl)acetamido)-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate. Molecular Formula: C32H36N6O8S2·2Na. Mole Weight: 742.77. Catalog: APB02824. | |
| Ampicillin EP Impurity F | Ampicillin EP Impurity F. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: sodium (4S)-2-(((R)-2-amino-2-phenylacetamido)methyl)-5,5-dimethylthiazolidine-4-carboxylate. Molecular Formula: C15H20N3NaO3S. Mole Weight: 345.39. Catalog: APB02831. | |
| Ampicillin EP Impurity M | Ampicillin EP Impurity M. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 114977-84-3(Free Acid); sodium (4S,4'S)-2,2'-((1R,7R,13R)-1-amino-14-(((2S,5R,6R)-2-carboxylato-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptan-6-yl)amino)-2,5,8,11,14-pentaoxo-1,7,13-triphenyl-3,6,9,12-tetraazatetradecane-4,10-diyl)bis(5,5-dimethylthiazolidine-4-carboxylate. CAS No. 94659-48-0. Molecular Formula: C48H54N9Na3O12S3. Mole Weight: 1114.16. Catalog: APB94659480. | |
| 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 |
| 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. | |
| Carbenicillin Disodium | Carbenicillin is a semi-synthetic penicillin antibiotic which interferes with cell wall synthesis of gram-negative bacteria while displaying low toxicity. The carboxypenicillins are susceptible to degradation by beta-lactamase enzymes, although they are more resistant than ampicillin to degradation. Carbenicillin is also more stable at lower pH than ampicillin. Synonyms: (2S,5R,6R)-6-[(2-Carboxy-2-phenylacetyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt; N-(2-Carboxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-6-yl)-2-phenylmalonamic Acid Disodium Salt; Anabactyl; Carbapen; Carbecin; Carbenicilline Disodium; Carboxybenzylpenicillin Sodium; Fugacillin; Geocillin; Geopen; Gripenin; Hyoper; Microcillin; NSC 111071; Piopen; Pyopen; α-Carboxybenzylpenicillin Sodium Salt; BRL-2064; BRL 2064; BRL2064. Grades: ≥90%. CAS No. 4800-94-6. Molecular formula: C17H16N2Na2O6S. Mole weight: 422.36. | |
| 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. | |
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