Description
Residual Solvents Mixture - Class I
Pharmaceutical Secondary Standard; Certified Reference Material
Properties
Properties
Related Categories | Additional Standards, Analytical Standards, Analytical/Chromatography, Application Areas and Market Segments, Chromatography, I-Z, Method and Regulation Specific, Neats and Solutions, Pharma, Pharmaceutical Secondary Standards, Pharmaceutical and Drug Standards, Pharmacopeia & Metrological Institutes Standards, Residual Solvent Standards, Residual Solvents Standards, Residue Solvents, Secondary Pharmaceutical Standards, USP |
grade | certified reference material |
pharmaceutical secondary standard | |
concentration | in DMSO |
suitability | suitable for 467 per USP |
Featured Industry | Environmental Pharmaceutical (small molecule) |
format | multi-component solution |
pharmacopeia traceability | traceable to PhEur R0250000 |
traceable to USP 1601102 |
General description
Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
Application
These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.
Analysis Note
These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.
Other Notes
This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025.
Description |
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Benzene 11 mg/mL |
Carbon tetrachloride 20 mg/mL |
1,2-Dichloroethane 27 mg/mL |
1,1-Dichloroethene 25 mg/mL |
1,1,1-Trichloroethane 50 mg/mL |
Safety Information