Description
Atorvastatin impurity F is a defined chemical reference material supplied at a minimum purity of 95 % for laboratory and analytical work. It is identified by CAS number 1371615-56-3 and the empirical formula C₄₀H₄₇FN₃O₈Na, with a molar mass of 739,8 g/mol. These identifiers support unambiguous substance tracking in impurity profiling, method development, and comparative analytical studies related to atorvastatin chemistry. The material is Clear labelling of CAS, formula, and molar mass helps laboratories document identity and batch use in research notebooks and quality systems. Sourced from manufacturer Carl ROTH, this impurity grade fits biochemical and impurity-focused workflows that demand a characterised solid for reference purposes. Use the stated molecular data when calculating concentrations, preparing calibration materials, or cross-checking spectral and chromatographic results against known structural parameters in routine or investigative laboratory practice.
This article is part of Chromatography standards (GC, HPLC, pesticides), in Analytical standards & reference materials.
Key features
- Assay: ≥ 95 %
- Colour: reported
- Form: reported
- CAS number: 1371615-56-3
- Pack sizes: 1 mg, 2 mg, 5 mg, 10 mg, 25 mg
- Purity: min. 95 %
- Empirical formula: C₄₀H₄₇FN₃O₈Na
- Molar mass: 739,8 g/mol
- Product type: Atorvastatin impurity F
- Technical Information Sheet:
- Safety Data Sheet:
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Questions about Atorvastatin impurity F, min. 95 %, 1 mg
What is this article?
Atorvastatin impurity F, min. 95 %, 1 mg is the article on this page. Luminix Health distributes Carl Roth for laboratory use. It sits in Chromatography standards (GC, HPLC, pesticides), inside Analytical standards & reference materials, in Lab chemicals.
A chromatography standard is the substance, or the mix, injected so a peak can be named and quantified. Pesticide mixes, residual-solvent mixes and single-compound standards are different articles. The concentration and the solvent are the specification. The solvent has to be one the method may contain.
A reference material is the article against which another result is compared. Its value is stated, and the uncertainty of that value is part of the product. An ICP or ion standard is a solution of known concentration. A volumetric standard is for titration. A chromatography standard is the peak you match. The grade names, including pharmacopoeia and ASTM, say which impurities were limited. Identity is checked on PubChem. Names follow IUPAC. Medicinal grades follow the European Pharmacopoeia and USP.
Which category should I open next?
The category is Analytical standards & reference materials. The sub-category is Chromatography standards (GC, HPLC, pesticides). The catalogue is Lab chemicals.
Shelves beside this one are ICP, AAS & ion standards, Reference substances & reagents (other), Volumetric standard solutions (titration), Reagents for analysis (Ph. Eur., ASTM, DIN), Spectroscopy & physical property standards and Indicators & indicator solutions.
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