Products
Pharmaceutical-Grade Absolute Ethanol
Purity: 99.9% (Pharmaceutical Grade)
Specifications:
- Conforms to IP/BP/USP standards
- Specific Gravity: 0.789 – 0.791 at 25°C
- Water Content: ≤0.2% (w/w)
- Residue on Evaporation: ≤0.001%
- Acidity/Alkalinity: Passes test
- Methanol Content: ≤200 ppm
Applications:
- API extraction and purification
- Pharmaceutical excipient in oral solutions, syrups, and tinctures
- Solvent for injectable formulations
- Vaccine production and mRNA therapies
- Biotechnology and drug delivery systems
- Medical-grade disinfectants and sanitizers
- Pharmaceutical manufacturing processes
Analytical Reagents
Purity: AR/ACS Grade
Specifications:
- Purity: ≥99.5%
- Assay: Meets AR/ACS grade standards
- Non-volatile Matter: ≤0.001%
- Acidity (as CH₃COOH): ≤0.002%
- Water Content: ≤0.5%
- UV Absorbance: Compliant with analytical standards
Applications:
- Instrumental analysis (HPLC, GC, UV-Vis)
- Spectroscopy and chromatography
- Analytical method development
- Quality control testing
- Reference standard preparation
- Research and development laboratories
Laboratory Reagents for HPLC Analysis
Purity: HPLC Grade / Gradient Grade
Specifications:
- Purity: ≥99.5%
- Assay: Meets AR/ACS grade standards
- Non-volatile Matter: ≤0.001%
- Acidity (as CH₃COOH): ≤0.002%
- Water Content: ≤0.5%
- UV Absorbance: Compliant with analytical standards
Applications:
- Instrumental analysis (HPLC, GC, UV-Vis)
- Spectroscopy and chromatography
- Analytical method development
- Quality control testing
- Reference standard preparation
- Research and development laboratories
Clinical & Diagnostic Reagents
Purity: Clinical Laboratory Grade
Specifications:
- Purity: ≥99.5%
- Free from interfering substances
- Sterility: Meets requirements (where applicable)
- Endotoxin Level: <0.5 EU/ml (for critical applications)
- pH Range: 6.5 – 7.5 (as applicable)
Applications:
- Clinical chemistry testing
- Hematology and immunology assays
- Microbiology culture preparation
- Diagnostic test kits
- Medical laboratory procedures
- Patient sample analysis
- Quality control in clinical settings
Pharmaceutical Laboratory Reagents
Purity: Pharmaceutical Grade (IP/BP/USP)
Specifications:
- Purity: ≥99.8%
- Heavy Metals: ≤5 ppm
- Sulfate: ≤10 ppm
- Chloride: ≤10 ppm
- Residue on Ignition: ≤0.005%
- Complies with pharmacopeial monographs
Applications:
- Pharmaceutical quality control testing
- Stability studies
- Dissolution testing
- Content uniformity analysis
- Impurity profiling
- Formulation development
- Validation and compliance testing