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It is produced by the strain of Cephalosporium aceemonium, C. salmosynnematum, Emericellopsis salmosynnemata. It has weak anti-gram-positive bacteria (activity against Staphylococcus aureus is only 1% of penicillin G) and anti-gram-negative bacteria activity, and can be broken down by penicillinase and cross-resistant to penicillin G. Synonyms: Penicillin N; Synnematin B; Cephalosporin N; Adicillin; Salmotin; SYNNEMATINB; Adicillinum; Synnematin N; (2S,5R,6R)-6-(5-Amino-5-carboxyvaleramido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptan-2-carbonsaeure; Cephalosphorin R; 6-N- ( (5-Amino-5-carboxy) pentanoyl) aminopenicillansaeure; (4-Amino-4-carboxybutyl)penicillin; NSC 113137; (D-4-Amino-4-carboxybutyl) penicillinic acid. Grades: 95%. CAS No. 525-94-0. Molecular formula: C14H21N3O6S. Mole weight: 359.40.
Penicillin
Penicillin. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: sodium (2S,5R,6R)-3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate. Molecular Formula: C16H17N2NaO4S. Mole Weight: 356.37. Catalog: APB02666.
penicillin amidase
This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. The systematic name of this enzyme class is penicillin amidohydrolase. Other names in common use include penicillin acylase, benzylpenicillin acylase, novozym 217, semacylase, alpha-acylamino-beta-lactam acylhydrolase, and ampicillin acylase. This enzyme participates in penicillin and cephalosporin biosynthesis. Group: Enzymes. Synonyms: penicillin acylase; benzylpenicillin acylase; novozym 217; semacylase; α-acylamino-β-lactam acylhydrolase; ampicillin acylase. Enzyme Commission Number: EC 3.5.1.11. CAS No. 9014-6-6. Penicillin Amidase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4389; penicillin amidase; EC 3.5.1.11; 9014-06-6; penicillin acylase; benzylpenicillin acylase; novozym 217; semacylase; α-acylamino-β-lactam acylhydrolase; ampicillin acylase. Cat No: EXWM-4389.
Penicillin amidase
Penicillin amidase is an enzyme used commercially for the production of semisynthetic penicillins. Synonyms: Amidase, penicillin; E.C. 3.5.1.11; Penicillin acylase; Benzylpenicillin acylase; Penicillin V acylase; Acylase, penicillin; Penicillin amidohydrolase; Penicillin G acylase. Grades: Activity wet form: 160U/g; Water content: 45%~60%. CAS No. 9014-6-6.
Penicillin amidase, E. coli
Penicillin amidase (EC 3.5.1.11) (Penicillin acylase) is an enzyme that cleaves the acyl side chains of penicillins. Penicillin amidase can be used for the production of 6-aminopenicillanic acid. Penicillin amidase can also be used in the resolution of racemic mixtures, peptide synthesis, and synthesis of semi-synthetic β-lactam antibiotics [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PGA. CAS No. 9014-6-6. Pack Sizes: 100 mg; 250 mg. Product ID: HY-P2834.
Penicillinase
Penicillinase is a beta-lactamase. beta-lactamase enzymes inactivate beta-lactam antibiotics by hydrolyzing the peptide bond of the characteristic four-membered beta-lactam ring rendering the antibiotic ineffective [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 9001-74-5. Pack Sizes: 5 mL. Product ID: HY-E70012.
Penicillin DF
Penicillin DF is used to characterize phenylacetate-CoA ligase from Penicillium chrysogenum. Group: Biochemicals. Grades: Highly Purified. CAS No. 4493-18-9. Pack Sizes: 10mg, 50mg. Molecular Formula: C14H22N2O4S, Molecular Weight: 314.399999999999. US Biological Life Sciences.
An impurity of Penicillin Potassium which which shows bactericidal property by acting directly on peptidoglycans. Synonyms: (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[(1-oxo-3-hexen-1-yl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Potassium Salt; 2-Pentenylpenicillin Potassium Salt; Penicillin I Potassium Salt; 6-(3-Hexenamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Potassium Salt. Grades: 95%. CAS No. 97299-13-3. Molecular formula: C14H19N2O4S.K. Mole weight: 350.47.
Penicillin F Sodium
It is produced by the strain of Penicillium notatum NRRL 1209, Pen. chrysogenum NRRL 1951. It is an antibiotic. Synonyms: Sodium penicillin F; 2-Pentenylpenicillin sodium; Sodium 2-pentenylpenicillinate; Penicillin F sodium salt; 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-((1-oxo-3-hexenyl)amino)-, monosodium salt, (2S-(2alpha,5alpha,6beta))-. CAS No. 525-86-0. Molecular formula: C14H19N2O4SNa. Mole weight: 334.37.
Penicillin G
Penicillin G is a β-lactam antibiotic produced by penicillin. Synonyms: Benzylpenicillin; Benzylpenicillinic Acid; Free Penicillin II. CAS No. 61-33-6. Molecular formula: C16H18N2O4S. Mole weight: 334.39.
Penicillin G benzathine
Penicillin G benzathine (Benzathine benzylpenicillin) is an antibiotic against many bacterial infections [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Benzathine benzylpenicillin. CAS No. 1538-09-6. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-N7139A.
Penicillin G Benzathine
An impurity of Penicillin G which is an antibacterial drug (intravenous use) against a wide range of bacteria. Uses: Anti-bacterial agents. Synonyms: Penicillin G benzathine (USP); (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid compound with N,N'-dibenzylethylenediamine (2:1), tetrahydrate; Permapen (TN); Wycillin (TN); Bis[(2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate]N,N'-Bis(phenylmethyl)-1,2-ethanediamine Tetrahydrate; Bis[[2S-(2α,5α,6β)]-3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate] N,N'-Bis(phenylmethyl)-1,2-ethanediamine Tetrahydrate. Grades: 97%. CAS No. 41372-02-5. Molecular formula: C16H20N2.2(C16H18N2O4S).4H2O. Mole weight: 981.18.
Penicillin G benzathine anhydrous
Penicillin G benzathine anhydrous. Group: Biochemicals. Alternative Names: Benzathine benzylpenicillin; Benzylpenicillin benzathine. Grades: Highly Purified. CAS No. 1538-09-6. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C16H20N2·2 (C16H18N2O4S). US Biological Life Sciences.
Worldwide
Penicillin G Clemizol
An impurity of Penicillin G which is used to treat many different types of infections caused by bacteria, such as ear infections. Synonyms: Clemizole penicillin; 6011-39-8; Clemizolpenicillin; 5UL276H6TF; Benzylpenicillin combined with 1-p-chlorobenzyl-2-(1-pyrrolidinylmethyl)benzimidazole; Penicillinclemizolum; 1-[(4-chlorophenyl)methyl]-2-(pyrrolidin-1-ylmethyl)benzimidazole; (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; Clemizole Penicillin G; Antihistamin-Penicillin-G; UNII-5UL276H6TF; Neopenyl; Clemizole penicillin [INN:BAN]; Clemizol-penicilina [INN-Spanish]; Clemizole penicilline [INN-French]; Clemizolum penicillinum [INN-Latin]; Clemizol-penicillin grunenthal; DTXSID10975533; CLEMIZOLE PENICILLIN [MART.]; CLEMIZOLE PENICILLIN [WHO-DD]; Q27123267; 6-[(1-Hydroxy-2-phenylethylidene)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid--1-[(4-chlorophenyl)methyl]-2-[(pyrrolidin-1-yl)methyl]-1H-benzimidazole (1/1). Grades: > 95%. CAS No. 6011-39-8. Molecular formula: C19H20ClN3.C16H18N2O4S. Mole weight: 325.84 334.40.
Penicillin G potassium
Cas No. 113-98-4.
Penicillin G potassium
Penicillin G potassium is a fast-acting penicillin family antibiotic. Penicillin G potassium can be used for the research of bacterial infections that affect the blood, heart, lungs, joints, and genital areas [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Benzylpenicillin potassium. CAS No. 113-98-4. Pack Sizes: 5 g; 10 g. Product ID: HY-17591.
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.
Worldwide
Penicillin G potassium salt (Benzylpenicillin potassium salt)
25g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17KN2O4S. CAS No. 113-98-4. Prepack ID 23531529-25g. Molecular Weight 372.48. See USA prepack pricing.
Penicillin G potassium (Standard)
Penicillin G (potassium) (Standard) is the analytical standard of Penicillin G (potassium). This product is intended for research and analytical applications. Penicillin G potassium is a fast-acting penicillin family antibiotic. Penicillin G potassium can be used for the research of bacterial infections that affect the blood, heart, lungs, joints, and genital areas [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 113-98-4. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17591R.
Penicillin G Procaine
An impurity of Penicillin G which is an antibacterial drug (intravenous use) against a wide range of bacteria. Uses: Anti-bacterial agents. Synonyms: Procaine Penicillin G Hydrate; (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[(phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid compd. with 2-(Diethylamino)ethyl 4-Aminobenzoate Hydrate; p-Aminohydratebenzoic Acid 2-(Diethylamino)ethyl Ester Mono[3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate] Monohydrate; Benzylpenicillin Procaine Monohydrate. Grades: > 95%. CAS No. 6130-64-9. Molecular formula: C16H18N2O4S. C13H20N2O2. Mole weight: 570.72.
Penicillin G procaine hydrate
Penicillin G Procaine hydrate (PGP hydrate), a β-lactam antibiotic , is a crystalline complex produced by chemically combining penicillin G with procaine [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PGP hydrate. CAS No. 6130-64-9. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-N7120.
Penicillin G sodium salt
It is produced by the strain of Penicillium notatum NRRL 1209, Pen. chrysogenum NRRL 1951. It has strong activity of anti-gram-positive bacteria and spirochetes, and has weak anti-gram-negative bacteria activity. It is widely used in clinical practice. Uses: Anti-bacterial agents. Synonyms: (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt; 3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Monosodium Salt; American Penicillin; Benzylpenicillin Sodium; Benzylpenicillin Sodium Salt; Benzylpenicillinic Acid Sodium Salt; Crystapen; Ethacillin; Monocillin; Monosodium Benzylpenicillin; Mycofarm; Nalpen G; Nobak; Novocillin; Pen-A-Brasive; Penicillin G Sodium; Penilaryn; Sodium 6-(Phenylacetamido)penicillanate; Sodium Benzylpenicillin; Sodium Benzylpenicillin G; Sodium Penicillin; Sodium Penicillin G; NSC 69877; NSC-69877; NSC69877; 7-NO2-ICA. Grades: 98%. CAS No. 69-57-8. Molecular formula: C16H17N2NaO4S. Mole weight: 356.37.
Penicillin G sodium salt
Penicillin G sodium salt is a typical β-lactam antibiotic. Uses: Scientific research. Group: Natural products. Alternative Names: Benzylpenicillin sodium salt. CAS No. 69-57-8. Pack Sizes: 100 mg. Product ID: HY-B1463.
Penicillin G sodium salt (Benzylpenicillin sodium salt)
25g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17N2NaSO4. CAS No. 69-57-8. Prepack ID 47080913-25g. Molecular Weight 356.37. See USA prepack pricing.
Penicillin G sodium salt (Benzylpenicillin sodium salt)
5g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17N2NaSO4. CAS No. 69-57-8. Prepack ID 47080913-5g. Molecular Weight 356.37. See USA prepack pricing.
Penicillin G, Sodium Salt USP
Penicillin G is a broad based antibiotic used in mammalian cell culture. Penicillin G blocks the formation of bacterial cell walls, rendering bacteria unable to multiply and spread. The spectrum of activity of Penicillin G includes many aerobic and anaerobic gram-positive organisms. Aerobes susceptible to Penicillin G include most beta-hemolytic streptococci, beta-lactamase-negative staphylococci, Actinomyces species, some Bacillus anthracis, Corynebacterium species, and Erysipelothrix rhusiopathiae. Most species of anaerobes, including Clostridium species, but excluding beta-lactamase-producing Bacteroides species, are also susceptible to Penicillin G. Penicillin G is easily ...id Monosodium Salt; (2S, 5R, 6R)-3, 3-dimethyl-7-oxo-6-[(phenylacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Monosodium Salt; American Penicillin; Benzylpenicillin Sodium; Benzylpenicillin Sodium Salt; Benzylpenicillinic Acid Sodium Salt; Crystapen; Ethacillin; Monocillin; Monosodium Benzylpenicillin; Mycofarm; Nalpen G; Nobak; Novocillin; Pen-A-Brasive; Penicillin G Sodium; Penilaryn; Sodium 6- (Phenylacetamido) penicillanate; Sodium Benzylpenicillin; Sodium Benzylpenicillin G; Sodium Benzylpenicillinate. Grades: USP. CAS No. 69-57-8. Pack Sizes: 50g, 100g, 500g, 1Kg. Molecular Formula: C16H17N2O4NaS, Molecular Weight: 356.37. US Biological Life Sciences.
Worldwide
Penicillin g sulfoxide p-methoxybenzyl ester
Penicillin g sulfoxide p-methoxybenzyl ester. Group: Biochemicals. Grades: Highly Purified. CAS No. 30034-13-0. Pack Sizes: 500mg, 1g, 2g, 5g. US Biological Life Sciences.
Worldwide
Penicillin Impurity 1
Penicillin Impurity 1 is an impurity of Penicillin. Penicillin belongs to the β-lactam class of antibiotics, is a very common antibacterial drug. Synonyms: (4S)-2t-((R)-amino-carboxy-methyl)-5,5-dimethyl-thiazolidine-4r-carboxylic acid. CAS No. 37727-80-3. Molecular formula: C8H14N2O4S. Mole weight: 234.27.
penicillin impurity 10
penicillin impurity 10. Uses: For analytical and research use. Group: Impurity standards. CAS No. 817553-80-3. Molecular Formula: C11H11NO4. Mole Weight: 221.21. Catalog: APB817553803.
penicillin impurity 11
penicillin impurity 11. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C32H38N4O9S2. Mole Weight: 686.8. Catalog: APB10858.
Penicillin Impurity 2
Penicillin Impurity 2 is an impurity of Penicillin. Penicillin belongs to the β-lactam class of antibiotics, is a very common antibacterial drug. Synonyms: 6-APA Dimer. Grades: 98%. CAS No. 1978372-79-0. Molecular formula: C16H24N4O6S2. Mole weight: 432.51.
penicillin impurity 3
penicillin impurity 3. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C32H36N4O8S2. Mole Weight: 668.78. Catalog: APB10854.
Penicillin Impurity 3
Penicillin Impurity 3 is an impurity of Penicillin. Penicillin belongs to the β-lactam class of antibiotics, is a very common antibacterial drug. Synonyms: 6α-chloropenicillanic acid 1,1-dioxide. CAS No. 76350-36-2. Molecular formula: C8H10ClNO5S. Mole weight: 267.69.
penicillin impurity 4
penicillin impurity 4. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C16H18N2O4S. Mole Weight: 334.39. Catalog: APB10855.
penicillin impurity 5
penicillin impurity 5. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C15H21ClN2O3S. Mole Weight: 344.85. Catalog: APB10856.
penicillin impurity 7
penicillin impurity 7. Uses: For analytical and research use. Group: Impurity standards. CAS No. 4493-18-9. Molecular Formula: C14H22N2O4S. Mole Weight: 314.4. Catalog: APB4493189.
penicillin impurity 8
penicillin impurity 8. Uses: For analytical and research use. Group: Impurity standards. CAS No. 3264-88-8. Molecular Formula: C16H18N2O4S. Mole Weight: 334.39. Catalog: APB3264888.
penicillin impurity 9
penicillin impurity 9. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C16H18N2O4S. Mole Weight: 334.39. Catalog: APB10857.
Penicillin potassium
Penicillin potassium. Uses: For analytical and research use. Group: Impurity standards. CAS No. 113-98-4. Molecular Formula: C16H17KN2O4S. Mole Weight: 372.48. Catalog: APB113984.
Penicillin sodium EPimpurity D
Penicillin sodium EPimpurity D. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C17H19NO4S. Mole Weight: 333.4. Catalog: APB10853.
Penicillin sodium EPimpurity F
Penicillin sodium EPimpurity F. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2714749-47-8. Molecular Formula: C15H20N2O3S. Mole Weight: 308.4. Catalog: APB2714749478.
Penicillin-Streptomycin Solution (100X)
An antibacterial solution comprised of penicillin (10,000 units/ml), a beta-lactam, and streptomycin (10,000 ug/ml), an aminoglycoside in 0.9% NaCl. Synonyms: D-Streptamine, O-2-deoxy-2-(methylamino)-alpha-L-glucopyranosyl-(1-2)-O-5-deoxy-3-C-formyl-alph-L-lyxofuranosyl-(1-4)-N,N'-bis(aminoiminomethyl)-, mixt. with (2S-(2alpha,5alpha,6beta))-3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid; Penicillin G mixture with Streptomycin (1:1). CAS No. 8025-6-7. Molecular formula: C16H18N2O4S.C21H39N7O12. Mole weight: 915.96.
Penicillin V
An impurity of Penicillin V which is used to treat many different types of infections caused by bacteria, such as ear infections (use by mouth). Uses: Penicillins. Synonyms: penicillin v; Phenoxymethylpenicillin; Penicillin phenoxymethyl; Oracillin; 87-08-1; Phenopenicillin; Phenomycilline; V-Cillin; Vebecillin; Fenospen; Distaquaine V; Phenoxymethyl penicillin; Meropenin; Calcipen; Fenacilin; Phenocillin; Phenoxymethylenepenicillinic acid; Stabicillin; Apopen; Oratren; Rocilin; Ospen;6beta-Phenoxyacetamido-2,2-dimethylpenam-3alpha-carboxylic acid; Phenoxymethylpenicillin, Antibiotic for Culture Media Use Only; Penicillin V, United States Pharmacopeia (USP) Reference Standard; Phenoxymethylpenicillin, European Pharmacopoeia (EP) Reference Standard; 4-THIA-1-AZABICYCLO(3.2.0)HEPTANE-2-CARBOXYLIC ACID, 3,3-DIMETHYL-7-OXO-6-((PHENOXYACETYL)AMINO)-, (2S-(2ALPHA,5ALPHA,6.BETA)).-. Grades: > 95%. CAS No. 87-08-1. Molecular formula: C16H18N2O5S. Mole weight: 350.4.
Penicillin V β-Sulfoxide-d3
Isotope labelled Penicillin V β-Sulfoxide, an intermediate in the synthesis of Penicillin V (P223500), an antibacterial agent. Group: Biochemicals. Alternative Names: 6-Phenoxyacetamidopenici llinic Acid-d3 1 β-Oxide; Penicillin-d3 V S-Oxide; [2S-(2α,4 β,5α,6 β )]-3, 3-Dimethyl-7-oxo-6-[(phenoxyacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid-d3 4-Oxide; (2S, 4S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(2-phenoxyacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid-d3 4-Oxide. Grades: Highly Purified. CAS No. 148680-07-3. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Penicillin V-d5
Antibacterial. Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(2-phenoxy-d5-acetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid; 6-(Phenoxy-d5-acetamido)penicillanic Acid; Phenoxy methyl penicillin-d5; Phenospen-d5; Oracilline-d5; V-Cillin-d5. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences.
Worldwide
Penicillin V-d5
Penicillin V-d 5 (Phenoxymethylpenicillin-d5) is the deuterium labeled Penicillin V. Penicillin V (Phenoxymethylpenicillin) is an orally active antibiotic. Penicillin V inhibits the growth of Streptococci, C. difficile and S. aureus. Penicillin V can be used for the research of otitis, sinusitis, pharyngitis and tonsillitis[1][2][3][4]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1356837-87-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-B0975AS.
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.
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.
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.
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.
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.
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.
Penicillin x (penicillin impurity 1). Uses: For analytical and research use. Group: Impurity standards. CAS No. 525-91-7. Molecular Formula: C16H18N2O5S. Mole Weight: 350.39. Catalog: APB525917.
Benzathine Benzyl Penicillin Impurity C
An impurity of Penicillin G which is an antibacterial drug (intravenous use) against a wide range of bacteria. Synonyms: Benzylpenicilloic acids Benzathine. Grades: > 95%. Molecular formula: C32H38N4O4S. Mole weight: 574.75.
Benzathine penicilline
Benzathine penicilline is an antibiotic useful for the treatment of a number of bacterial infections, which is also known as benzathine penicillin G. It has bacteriostatic and bacteriocidal actions against most Gram-positive bacteria and Gram-negative cocci. Uses: Anti-bacterial agents. Synonyms: Debecillin; Pendepon; Penduran. Grades: >98%. CAS No. 1538-09-6. Molecular formula: C48H56N6O8S2. Mole weight: 909.12.
Benzathine penicillin EP impurity D (Penicillin sodium EP impurity D/Carboxybenzylpenicillin sodium EP impurity I)
Benzathine penicillin EP impurity D (Penicillin sodium EP impurity D/Carboxybenzylpenicillin sodium EP impurity I). Uses: For analytical and research use. Group: Impurity standards. CAS No. 13093-87-3. Molecular Formula: C16H18N2O4S. Mole Weight: 334.39. Catalog: APB13093873.
Benzathine penicillin G tetrahydrate
100mg Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C48H56N6O8S2 · 4H2O. CAS No. 1538-09-6. Prepack ID 29031910-100mg. Molecular Weight 981.18. See USA prepack pricing.
Benzathine penicillin impurity 1
Benzathine penicillin impurity 1. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C15H16N2O4S. Mole Weight: 320.36. Catalog: APB10374.
Benzathine penicillin impurity 2
Benzathine penicillin impurity 2. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C16H18N2O4S. Mole Weight: 334.39. Catalog: APB10376.
Benzathine penicillin impurity 3
Benzathine penicillin impurity 3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 62730-81-8. Molecular Formula: C9H12N2. Mole Weight: 148.21. Catalog: APB62730818.
Benzathine penicillin impurity 4
Benzathine penicillin impurity 4. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C14H20KN2O4S. Mole Weight: 351.48. Catalog: APB10377.
Benzathine penicillin impurity 5
Benzathine penicillin impurity 5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 13057-98-2. Molecular Formula: C16H20N2O5S. Mole Weight: 352.41. Catalog: APB13057982.
Benzathine penicillin sodium
Benzathine penicillin sodium. Uses: For analytical and research use. Group: Impurity standards. CAS No. 69-57-8. Molecular Formula: C16H17N2NaO4S. Mole Weight: 356.37. Catalog: APB69578.
Benzylpenicillin
It is produced by the strain of Penicillum sp. Penicillin has a strong antibacterial effect on gram-positive bacteria, Neisseria, Haemophilus, anaerobes (except fragile bacilli), spirochetes and actinomycetes, but no effect on mycobacterium tuberculosis, rickettsia, fungi, protozoa and virus. Synonyms: penicillin g; Benzylpenicillinic acid; Pencillin G. Molecular formula: C16H18N2O4S. Mole weight: 334.39.
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.
Worldwide
Benzylpenicillin CP Impurity G
An impurity of Penicillin G which is an antibacterial drug (intravenous use) against a wide range of bacteria. Grades: > 95%. Molecular formula: C6H11NO3S. Mole weight: 177.22.
Benzylpenicillin CP Impurity I
An impurity of Penicillin G which is an antibacterial drug (intravenous use) and exerts a bacterial action against a wide range of bacteria. Grades: > 95%. Molecular formula: C17H19NO4S. Mole weight: 333.41.
Benzylpenicillin CP Impurity J
An impurity of Penicillin G which shows bactericidal property by acting directly on peptidoglycans. Grades: > 95%. Molecular formula: C17H20N2O6S. Mole weight: 380.42.
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