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Meets United States Pharmacopeia (USP) monograph requirements for purity and quality.
High assay content (>99.7% acetic acid), ensuring consistent performance in critical applications.
Low levels of heavy metals and trace impurities, supporting compliance with pharmaceutical and biotech standards.
Manufactured under strict cGMP conditions with full traceability and batch-specific Certificates of Analysis.
Available in secure, chemically resistant packaging suitable for aseptic handling and storage.
Active pharmaceutical ingredient (API) synthesis and purification processes.
Buffer component in parenteral and ophthalmic drug formulations.
pH adjustment and stabilization in biologics manufacturing and cell culture media.
Reagent in analytical testing laboratories for USP-compliant methods.
Intermediate in the production of high-purity acetate salts and esters for medical devices.
| Chemical Type | Glacial Acetic Acid |
| Product Form | Liquid |
| Appearance | Clear, colorless liquid |
| Assay (CH₃COOH) | ≥99.7% |
| Water Content | ≤0.25% |
| Residue on Ignition | ≤0.01% |
| Heavy Metals (as Pb) | ≤10 ppm |
| Identity Test | Conforms to USP monograph |
Contact With Us:
E-mail: wangxingqiang@ericwchem.com
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Building A1, Jiete Industrial Park, Huangpu District, Guangzhou City, Guangdong Province, China
