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Penicillin V potassium United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. Alfa Chemistry Analytical Products 2
Penicillin V Potassium Penicillin V Potassium (Phenoxymethylpenicillin potassium salt) is an orally active antibiotic. Penicillin V Potassium inhibits the growth of Streptococci , C. difficile and S. aureus. Penicillin V Potassium can be used for the research of otitis, sinusitis, pharyngitis and tonsillitis [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: Phenoxymethylpenicillin potassium salt. CAS No. 132-98-9. Pack Sizes: 5 g; 10 g. Product ID: HY-B0975. MedChemExpress MCE
Penicillin V potassium salt 100g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17KN2O5S. CAS No. 132-98-9. Prepack ID 55440700-100g. Molecular Weight 388.48. See USA prepack pricing. Molekula Americas
Penicillin V potassium salt 25g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17KN2O5S. CAS No. 132-98-9. Prepack ID 55440700-25g. Molecular Weight 388.48. See USA prepack pricing. Molekula Americas
Penicillin V potassium salt analytical standard. Group: Application areas. Alfa Chemistry Analytical Products 4
Penicillin V Potassium Salt Antibacterial. Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(2-phenoxyacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Potassium; 6- (Phenoxyacetamido) penicillanic Acid Potassium; Antibiocin. Grades: Highly Purified. CAS No. 132-98-9. Pack Sizes: 100mg. US Biological Life Sciences. USBiological 2
Worldwide
Penicillin V Potassium Salt The Potassium Salt form of Penicillin V is an orally active penicillin that has been found to be an effective antibiotic against sorts of bacteria. Uses: Penicillins. Synonyms: (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[(2-phenoxyacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Potassium; 6-(Phenoxyacetamido)penicillanic Acid Potassium; Antibiocin; Calciopen K; Cilacil; Fenoxypen; Vepicombin; 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-(2-phenoxyacetamido)-, (2S,5R,6R)-, Potassium salt. Grades: 96%. CAS No. 132-98-9. Molecular formula: C16H17KN2O5S. Mole weight: 388.48. BOC Sciences 6
Penicillin V Potassium USP Phenoxymethylpenicillin Potassium, 3,3-dimethyl-7-oxo-6-(2-phenoxy-acetamido)-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid mono Potassium salt. Grades: USP. CAS No. 132-98-9. Product ID: 8-01823. Molecular formula: C16H17N2O5SK. Mole weight: 388.5. CarboMer Inc
Penicillin V-d5 potassium Penicillin V-d 5 (potassium) is the deuterium labeled Penicillin V Potassium[1]. Penicillin V Potassium (Phenoxymethylpenicillin potassium salt) is an orally active antibiotic. Penicillin V Potassium inhibits the growth of Streptococci, C. difficile and S. aureus. Penicillin V Potassium can be used for the research of otitis, sinusitis, pharyngitis and tonsillitis[2][3][4][5]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: Phenoxymethylpenicillin-d5 potassium salt. CAS No. 2699607-22-0. Pack Sizes: 1 mg. Product ID: HY-B0975S1. MedChemExpress MCE
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. Creative Enzymes
Penicillin G Potassium Salt Penicillin G is a narrow spectrum antibiotic derived from Streptococcus pneumoniae. It is the drug of choice for groups A, B, C and G streptococci, nonenterococcal group D streptococci, viridians group streptococci, and non-penicillinase producing staphylococcus. The potassium salt has been used to study murosomes of staphylococci† and the penicillin-induced lysis of Streptococcus mutans. Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Potassium Salt; Penicillin G Potassium Salt; Benzylpenicillin Potassium; Cosmopen; Cristapen; Crytapen; Eskacillin; Falapen; Forpen; Hipercilina; Hyasorb; Hylenta; M-Cillin; Monopen; NSC 131815; Notaral; Pentid; Pentids; Potassium 6- (Phenylacetamido) penicillanate; Potassium Benzylpenicillin; Potassium Benzylpenicillinate; Potassium Penicillin G; Scotcil; Tabilin. Grades: Cell Culture Grade. CAS No. 113-98-4. Pack Sizes: 100g, 500g, 1Kg. US Biological Life Sciences. USBiological 1
Worldwide
Phenoxymethylpenicillin Potassium Impurity D An impurity of Penicillin Potassium which shows bactericidal property against penicillin-sensitive microorganisms during the stage of active multiplication. Synonyms: 6-[2-(p-Hydroxyphenoxy)acetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid; (2S,5R,6R)-6-[[(4-Hydroxyphenoxy)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid; [2S-(2α,5α,6β)]-6-[[(4-Hydroxyphenoxy)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid; (4-Hydroxyphenoxy)methylpenicillin; (p-Hydroxyphenoxy)methylpenicillin; 4-Hydroxypenicillin V; p-Hydroxypenicillin V. Grades: > 95%. CAS No. 20880-67-5. Molecular formula: C16H18N2O6S. Mole weight: 366.4. BOC Sciences 7
Phenoxymethylpenicillin Potassium Impurity E An impurity of Penicillin Potassium which is an antibacterial drug (intravenous use) and exerts a bacterial action against a wide range of bacteria. Synonyms: Penicilloic V Acid; 1049-84-9; 2-[carboxy-[(2-phenoxyacetyl)amino]methyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid; NSC163496; phenoxomethylpenicilloyl; 2-(Carboxy(2-phenoxyacetamido)methyl)-5,5-dimethylthiazolidine-4-carboxylic acid; Penicilloic acid V; NSC 74505; NSC 163496; (Phenoxymethyl) penicilloic Acid; DTXSID20909263; CHEBI:190081; NSC74505; NSC-74505; NSC-163496; 2-Thiazolidineacetic acid, 4-carboxy-5,5-dimethyl-alpha-((phenoxyacetyl)amino)-; FT-0673557; J-001326; 4-Carboxy-5,5-dimethyl-alpha-[(2-phenoxyacetyl)amino]-2-thiazolidineacetic Acid; 1049-83-8; 2-{Carboxy[(1-hydroxy-2-phenoxyethylidene)amino]methyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid. Grades: > 95%. CAS No. 1049-84-9. Molecular formula: C16H20N2O6S. Mole weight: 368.41. BOC Sciences 7
Benzylpenicillinate-d7, Potassium Salt Benzylpennicillin (penicillin G) is a widely used antibiotic in veterinary medicine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. USBiological 1
Worldwide

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