Kanamycin, deoxy-

Specifications

• CAS Number: 5487-00-3
• Purity: ≥ 94 % HPLC
• Grade: Industrial grade
• Molecular Formula: C18H36N4O10
• Molecular Weight: 468.5 g/mol
• Appearance: A white to off-white, odorless, crystalline powder.
• Application: A broad-spectrum aminoglycoside antibiotic.

Documentation

• Certificate of Analysis (COA)
• Safety Data Sheet (SDS)

Production Manufacturer

Palkem India, based in Mumbai, India, is a prominent chemical company recognized for its reliable supply of high-quality chemicals across diverse industries. With a strong focus on customer satisfaction and continuous improvement, Palkem India has earned a reputation as a preferred supplier within the chemical sector. Offering an extensive product range, dependable delivery, and responsive customer service, Palkem India is well-positioned for ongoing growth and success.

Physicochemical properties

Physical Parameters

Parameter	Value / Description
Melting Point (MP)	-
Boiling Point (BP)	-
Density	-
Specific Gravity	-
Solubility	Soluble in water
Refractive Index	-
Vapor Pressure	Very low (typical for solid, ionic organic compounds).
Viscosity	-
Phase at Room Temperature	Solid (typically a white or off-white crystalline powder, often as a sulfate salt).

Chemical Parameters

Parameter	Value / Description
Chemical Stability	Stable under normal storage conditions. Likely hygroscopic as a salt. Aminoglycosides are generally stable in acidic and basic formulations but can be susceptible to thermal degradation.
Flash Point	-
Chemical Reactivity	Reactivity typical of an aminoglycoside: contains multiple amino groups (basic) and hydroxyl groups. The 6'-deoxy modification reduces susceptibility to certain phosphorylating enzymes.
Functional Groups	Amino groups (–NH₂), hydroxyl groups (–OH), glycosidic linkages
Spectroscopic Data (IR, NMR, etc.)	Mass Spec (MS): Molecular formula C₁₈H₃₆N₄O₁₀ (for free base). Parent ion m/z consistent with formula. NMR (¹H & ¹³C): Spectra would show characteristic signals for the 2-deoxystreptamine ring and sugar protons, with a key absence of the signal for the 6'-hydroxyl proton and a methylene signal (6'-CH₂) instead of a methine. Specific chemical shift values not publicly cataloged. IR: Broad absorption for -OH and -NH stretches, characteristic carbohydrate fingerprint region.

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