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Meets stringent United States National Formulary (NF) and European Pharmacopoeia (EP) monograph requirements for pharmaceutical-grade solvents.
High purity with low levels of residual water, aldehydes, and heavy metals—ensuring compatibility with sensitive API synthesis and formulation processes.
Consistent batch-to-batch quality supported by rigorous in-house testing and full traceability documentation.
Versatile solvent performance across a wide temperature range with favorable evaporation rate and low toxicity profile.
Produced under cGMP-aligned manufacturing practices with dedicated pharma-grade production lines.
Active pharmaceutical ingredient (API) crystallization and purification.
Solvent for coating formulations in oral solid dosage forms (e.g., film-coated tablets).
Extraction medium in natural product isolation and botanical processing.
Component in topical and transdermal drug delivery systems requiring volatile, non-toxic solvents.
Intermediate solvent in peptide synthesis and oligonucleotide manufacturing.
| Chemical Type | Ethyl acetate |
| Product Form | Liquid |
| Appearance | Clear, colorless liquid |
| Odor | Characteristic fruity odor |
| Primary Applications | Pharmaceutical synthesis, extraction, and formulation |
| Key Features | Pharmacopoeial grade (NF/EP compliant), low residual impurities |
| Storage Recommendation | Store in tightly closed containers away from heat and ignition sources |
| Regulatory Status | Complies with USP-NF, Ph. Eur., and ICH Q3C guidelines |
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E-mail: wangxingqiang@ericwchem.com
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Building A1, Jiete Industrial Park, Huangpu District, Guangzhou City, Guangdong Province, China
