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6-Aminopenicillanic acid 100g Pack Size. Group: Bioactive Small Molecules, Aroma Chemicals, Building Blocks. Formula: C8H12N2O3S. CAS No. 551-16-6. Prepack ID 13631841-100g. Molecular Weight 216.26. See USA prepack pricing. Molekula Americas
6-Aminopenicillanic acid 6-Aminopenicillanic acid (6-APA) is an important precursor for the synthesis of b-lactam antibiotics. 6-Aminopenicillanic acid is the main product of Penicillin G (PenG) hydrolyzed by penicillin acylase (PA) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 6-APA. CAS No. 551-16-6. Pack Sizes: 500 mg. Product ID: HY-W013549. MedChemExpress MCE
6-Aminopenicillanic acid 6-Aminopenicillanic acid (6-APA) is an important precursor for the synthesis of lactam antibiotics. 6-Aminopenicillanic acid is the main product of Penicillin G (PenG) hydrolyzed by penicillin acylase (PA). Uses: Designed for use in research and industrial production. Additional or Alternative Names: (25,5R,6R)-6-AMINO-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID;(2S,5R,6R)-6-AMINO-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO-[3.2.0]HEPTANE-2-CARBOXYLIC ACID;6-AMINO-2,2-DIMETHYL-5-OXOPERHYDROAZETO[2,1-B][1,3]THIAZOLE-3-CARBOXYLIC ACID;6-AMINO-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID;6-APA;(+)-6-AMINOPENICILLANIC ACID;6-AMINOPENICILLANIC ACID;6-AMINO PENICILLINIC ACID. Product Category: Inhibitors. Appearance: Solid. CAS No. 551-16-6. Molecular formula: C8H12N2O3S. Mole weight: 216.26. Purity: ≥98.0%. Canonical SMILES: [C@H]12SC([C@@H](N1C(=O)[C@H]2N)C(=O)O)(C)C. Product ID: ACM551166. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
6-Aminopenicillanic acid 6-Aminopenicillanic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 551-16-6. Pack Sizes: 25g, 50g, 100g. US Biological Life Sciences. USBiological 6
Worldwide
6-Aminopenicillanic acid It is produced by the strain of Peniclllun chrysogenum and Pleurotus ostreatus. 6-APA is the main raw material for semisynthesis of penicillin, and the key intermediates for semisynthesis of cephalosporin (7-ACA) and 7-amino-deacetylated ceosenoic acid (7-ADCA) can be generated by chemical or enzymatic ring expansion. Synonyms: 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. Grades: > 95%. CAS No. 551-16-6. Molecular formula: C8H12N2O3S. Mole weight: 216.26. BOC Sciences 6
(+)-6-Aminopenicillanic Acid (+)-6-Aminopenicillanic Acid is the core structure in penicillins, obtained from the fermentation brew of the Penicillium mold. (+)-6-Aminopenicillanic Acid is used as the main starting block for the preparation of numerous semisynthetic penicillins. Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-6-Amino-3, 3-dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid; 6-APA; 6-APS; 6 β-Aminopenicillanic acid; NSC 50071; [2S-(2α,5α,6 β )]-6-Amino-3, 3-dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid; Phenacyl 6-Aminopenicillinate. Grades: Highly Purified. CAS No. 551-16-6. Pack Sizes: 1g. US Biological Life Sciences. USBiological 2
Worldwide
Aspoxicillin Aspoxicillin is a semi-synthetic penicillin prepared from 6-aminopenicillanic acid (6-APA) or Amoxicillin. It has a broad antibacterial spectrum and has an effect on Pseudomonas aeruginosa. Synonyms: Aspoxicilina; Aspoxicilline; Aspoxicillinum. Grades: >98%. CAS No. 63358-49-6. Molecular formula: C21H27N5O7S. Mole weight: 493.53. BOC Sciences
BLP-1654 BLP-1654 is a semi-synthetic penicillin made from 6-aminopenicillanic acid (6-APA). It has anti-Gram-positive and negative bacteria activity, especially for Pseudomonas bacteria. Synonyms: 6- (D-alpha- (3-Guanylureido) phenylacetamido) penicillanic acid. Grades: >98%. CAS No. 28889-87-4. Molecular formula: C18H22N6O5S. Mole weight: 434.47. BOC Sciences 5
isopenicillin-N N-acyltransferase Proceeds by a two stage mechanism via 6-aminopenicillanic acid. Different from EC 3.5.1.11, penicillin amidase. Group: Enzymes. Synonyms: acyl-coenzyme A:isopenicillin N acyltransferase; isopenicillin N:acyl-CoA: acyltransferase. Enzyme Commission Number: EC 2.3.1.164. CAS No. 54576-90-8. 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-2104; isopenicillin-N N-acyltransferase; EC 2.3.1.164; 54576-90-8; acyl-coenzyme A:isopenicillin N acyltransferase; isopenicillin N:acyl-CoA: acyltransferase. Cat No: EXWM-2104. Creative Enzymes
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. MedChemExpress MCE

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