aozun
White or off white crystalline powder
546-88-3
C2H5NO2
75
208-913-8
soluble in water
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Product Description
Acetohydroxamic Acid, also known as N-hydroxyacetamide or AHA, is a low-molecular-weight organic hydroxamic acid. Its hydroxamic acid group can coordinate with metal ions, and the compound is widely used in urease research, pharmaceutical development, analytical work and specialty chemical synthesis.
Acetohydroxamic Acid may be supplied for pharmaceutical, research or synthesis applications. These grades are not automatically interchangeable, so buyers should confirm the specification, production controls and supporting documents before ordering.
Item | Information |
|---|---|
Product name | Acetohydroxamic Acid |
Abbreviation | AHA |
Synonym | N-Hydroxyacetamide; Acetylhydroxamic Acid |
CAS number | 546-88-3 |
Molecular formula | C₂H₅NO₂ |
Molecular weight | 75.07 g/mol |
Appearance | White to light-yellow powder or crystals |
Chemical family | Hydroxamic acids |
Chemical classification | Organic fine chemical |
Common roles | Urease inhibitor, research reagent and specialty synthesis material |
Appearance and analytical limits should be confirmed against the agreed specification and lot-specific Certificate of Analysis.
Material intended for pharmaceutical manufacturing requires more than a high assay result. Buyers should evaluate the manufacturing site, applicable quality system, impurity controls, residual solvents, elemental impurities, stability data and regulatory documents.
A material should not be described as API grade solely because its assay is 98% or higher. Pharmaceutical suitability must be confirmed for the intended market and manufacturing process.
Research-grade material may be used in urease inhibition studies, biochemical research, method development, analytical testing and coordination chemistry. Required purity and documentation depend on the research protocol.
Synthesis-grade Acetohydroxamic Acid may be used as a specialty reagent or building block in organic and coordination chemistry. Buyers should focus on assay, related substances, water content and batch consistency.
Acetohydroxamic Acid is known as an active pharmaceutical ingredient in a regulated prescription product. Material intended for this application must comply with the applicable pharmaceutical and market-specific requirements.
This page describes a B2B chemical raw material and does not provide medical advice, dosage instructions or a finished medicinal product.
Acetohydroxamic Acid is widely studied as a urease inhibitor. It is used in biochemical assays, enzyme-mechanism research and the development of analytical methods involving urease activity.
The hydroxamic acid functional group can interact with metal ions. This makes the compound useful in analytical studies, metal-binding research and coordination chemistry.
Acetohydroxamic Acid can also be used as a specialty reagent or intermediate in selected laboratory and fine-chemical synthesis processes.
Assay alone does not establish whether Acetohydroxamic Acid is suitable for pharmaceutical, analytical or synthesis use.
Quality attribute | Why it matters |
Identification | Confirms the chemical identity using methods such as IR or chromatography |
Assay | Measures the amount of Acetohydroxamic Acid in the sample |
Related substances | Controls process impurities and degradation products |
Water or loss on drying | Supports stability, handling and accurate formulation |
Melting range | Provides an additional identity and purity indication |
Residual solvents | Important when solvents are used during production |
Elemental impurities | May be required for pharmaceutical or sensitive applications |
Appearance and solution clarity | Helps identify contamination or degradation |
Particle size | May affect dissolution, processing or formulation performance |
Microbiological quality | Considered when required by the final pharmaceutical application |
The final acceptance limits should be defined by the buyer’s application and included in the approved purchasing specification.
Depending on grade and application, buyers may request:
Lot-specific Certificate of Analysis
Safety Data Sheet
Technical Data Sheet or approved specification
Manufacturing and retest dates
Country-of-origin information
Packaging details
Analytical methods or chromatograms when available
Residual-solvent and elemental-impurity information
Stability or retest-period information
Manufacturer and quality-system documents for regulated applications
GMP, pharmacopeial compliance, DMF, ASMF or CEP availability should only be stated when the relevant document has been verified.
Keep Acetohydroxamic Acid in a tightly sealed container in a cool, dry and dark location. Protect it from moisture and incompatible materials. Some specifications may require storage under an inert atmosphere.
The material should be handled by trained personnel using suitable protective equipment. Always consult the current Safety Data Sheet before storage, sampling, processing or disposal.
Available packaging, transport conditions and shelf life should be confirmed with the quotation.
AOZUN helps customers match Acetohydroxamic Acid with the intended pharmaceutical, research or synthesis application. Product grade, specification, packaging, documentation and sample availability can be reviewed before order confirmation.
To receive an accurate quotation, provide:
Intended application
Required assay and impurity limits
Destination country
Estimated order quantity
Preferred packaging
Required quality and regulatory documents
All specifications and compliance statements remain subject to the confirmed quotation and manufacturer documentation.
It is an organic compound belonging to the hydroxamic acid family.
It is best classified as a fine chemical. It may also serve as a specialty synthesis intermediate, but “Organic Fine Chemical” is the recommended primary website category.
AHA is a commonly used abbreviation for Acetohydroxamic Acid. Because AHA can have other meanings, purchase documents should include the full name and CAS No. 546-88-3.
No. Assay alone does not demonstrate API suitability. Manufacturing controls, impurity limits, stability, documentation and regulatory requirements must also be evaluated.
Not automatically. Research-grade and pharmaceutical-grade materials have different production, testing and documentation requirements.
Contact AOZUN with your required grade, specification, quantity, destination and documentation needs. Our team will review the application and provide the appropriate product information, packaging options and quotation.