Aminoglycosides
Aminoglycosides are a class of antibiotics used against gram-negative bacterial infections, and this category covers reference standards built around kanamycin, tobramycin, and neomycin derivatives, including protected intermediates and process impurities. These standards support antibiotic drug development, impurity profiling for quality control, and structure confirmation work during multi-step synthesis of these complex molecules. Sourcing from a dedicated supplier means each aminoglycoside-related compound, however structurally complex, arrives with verified identity, documented purity, and a certificate of analysis.
Showing 1–16 of 75 results
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(2R,3R,4S,5R,6R)-2-((R)-1-Azidoethyl)-3,4,5-tris(benzyloxy)-6-chlorotetrahydro-2H-pyran-2-yl)-oxy)-tris-N-benzyloxycarbonyl Garamine
CAS Number: N/A
Molecular Formula: C65 H74 N6 O16
Catalogue Number: RCLS2L107962
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1-N-Ethylgaramine Sulfate
CAS Number: 864371-49-3
Molecular Formula: C15H31N3O6 .xH2SO4
Catalogue Number: RCLS2L142634
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1,3-Di-HABA Kanamycin A
CAS Number: 927821-99-6
Molecular Formula: C26 H50 N6 O15
Catalogue Number: RCLS2L133311
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1,3’’-Di-HABA Kanamycin A Sulfate
CAS Number: N/A
Molecular Formula: C26H50N6O15 xH2SO4
Catalogue Number: RCLS2L133312
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2,2,3,3,3-Pentafluoropropanoic Acid
CAS Number: 422-64-0
Molecular Formula: C3HF5O2
Catalogue Number: RCLS2L172493
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2,6-Diamino-2,3,6-trideoxy-D-ribo-Hexose Di-TFA Salt
CAS Number: N/A
Molecular Formula: C6H14N2O3 • 2(C2HF3O2)
Catalogue Number: RCLS2L130975
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3-Azido Neomycin B TFA Salt
CAS Number: N/A
Molecular Formula: C23H44N8O13. x C2HF3O2
Catalogue Number: RCLS2L107991
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3-N-Ureido Tobramycin Tetrahydrochloride Salt (1:2 mixture of 3-N-Ureido:1-N-Ureido, Technical Grade)
CAS Number: N/A
Molecular Formula: C19H38N6O10 • 4(HCl)
Catalogue Number: RCLS2L186217
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![3”-[N-(HABA-CBz)] 3,5,6′-Tri(N-Benzyloxycarbonyl) Kanamycin A](https://www.clinivex.com/wp-content/uploads/watermarked/269969-full.jpg?v=1788585574)
3''-[N-(HABA-CBz)] 3,5,6'-Tri(N-Benzyloxycarbonyl) Kanamycin A
CAS Number: N/A
Molecular Formula: C54H67N5O21
Catalogue Number: RCLS2L147909
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3’’-HABA Kanamycin A Sulfate
CAS Number: N/A
Molecular Formula: C22H43N5O13 xH2SO4
Catalogue Number: RCLS2L147908
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4-Methylumbelliferyl Di-N-Acetyl-Beta-D-chitobiose
CAS Number: 53643-12-2
Molecular Formula: C26 H34 N2 O13
Catalogue Number: RCLS2L164607
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4-Nitrophenyl N,N-Diacetyl-Beta-D-chitobioside
CAS Number: 7284-16-4
Molecular Formula: C22 H31 N3 O13
Catalogue Number: RCLS2L168825
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![4,6-Diamino-1,3a-dimethylhexahydro-2H-pyrano[4,3-d]oxazol-2-one](https://www.clinivex.com/wp-content/uploads/watermarked/238075-full.jpg?v=1788585574)
4,6-Diamino-1,3a-dimethylhexahydro-2H-pyrano[4,3-d]oxazol-2-one
CAS Number: N/A
Molecular Formula: C20 H36 N4 O11
Catalogue Number: RCLS2L130522
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![5-[N-(HABA-Cbz)] 3,6′-Di(N-benzyloxycarbonyl) Kanamycin A](https://www.clinivex.com/wp-content/uploads/watermarked/269971-full.jpg?v=1788585574)
5-[N-(HABA-Cbz)] 3,6'-Di(N-benzyloxycarbonyl) Kanamycin A
CAS Number: N/A
Molecular Formula: C46H61N5O19
Catalogue Number: RCLS2L147910
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6-O-Des(6-Amino-Alpha-D-gluocopyranosyl) 3-HABA Kanamycin A Sulfate
CAS Number: N/A
Molecular Formula: C16H32N4O9•xH2SO4
Catalogue Number: RCLS2L129329
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Acetylacetonatobis(ethylene)rhodium(I)
CAS Number: 12082-47-2
Molecular Formula: C9 H11 O2 Rh
Catalogue Number: RCLS2L100996
Aminoglycoside Reference Standards for Antibiotic Development and QC
Reliable aminoglycoside standards matter throughout antibiotic development and manufacturing, where confirming the identity of a protected intermediate or process impurity at each synthesis stage helps prevent costly errors from carrying through to the final product.
Clinivex supplies a range of aminoglycoside reference standards, including protected kanamycin, tobramycin, and neomycin derivatives, each backed by a certificate of analysis. Our technical team can help source related intermediates through our global supplier network as your synthesis or QC work requires.
As an ISO 9001:2015 and GMP certified supplier working with pharmaceutical manufacturers and quality control laboratories across the USA and Canada, we focus on accurate documentation and dependable delivery for every order.
Protecting group reagents used throughout this kind of synthesis are covered under additives and precursors. Antibiotic drug development more broadly is a recurring subject within pharmaceutical and biotech research.
Contact our team to request a quote or check availability for a specific aminoglycoside standard.
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Frequently Asked Questions
They work by binding to bacterial ribosomes and disrupting protein synthesis, making them effective against a range of gram-negative bacterial infections.
Aminoglycosides contain multiple reactive amine and hydroxyl groups, so protecting groups are used to control exactly which position reacts at each step of a complex, multi-step synthesis.
Because these molecules are structurally complex with many similar functional groups, closely related impurities can form during synthesis, making thorough impurity profiling essential for a safe, consistent final product.
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