O-Methyl atorvastatin calcium, min. 95 %, 1 mg

Catalog nr. 2P7P.1
Carl Roth

Volume: 1 mg
Value Packs: 1 piece
Price:
Sale price€435,40
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Description

O-Methyl atorvastatin calcium is a defined biochemical impurity standard offered at a minimum purity of 95 %, with CAS number 887196-29-4 and empirical formula CaC₆₈H₇₁F₂N₄O₁₀. Its molar mass of 1182,39 g/mol supports precise preparation of analytical solutions and reference materials in pharmaceutical and medicinal-chemistry laboratories. Analytical teams can deploy it in HPLC, LC-MS and related chromatographic workflows that demand a clearly specified calcium-salt derivative of the O-methylated statin scaffold. This material from manufacturer Carl ROTH fits quality-control, research and development settings that catalogue process-related or degradation impurities. The stated assay and molecular data help laboratories document reference identity and maintain consistent experimental design when comparing samples against known atorvastatin analogues.

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: 887196-29-4
  • Pack sizes: 1 mg, 2 mg, 5 mg, 10 mg, 25 mg
  • Purity: min. 95 %
  • Empirical formula: CaC₆₈H₇₁F₂N₄O₁₀
  • Molar mass: 1182,39 g/mol
  • Storage temperature: -20 °C
  • Technical Information Sheet: PDF
  • Safety Data Sheet: PDF

Compliance & Safety Information

GHS07, harmfulWarning

Hazard Statements (H-Phrases)

H302Harmful if swallowed.

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Questions about O-Methyl atorvastatin calcium, min. 95 %, 1 mg

What is this article?

O-Methyl atorvastatin calcium, 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.

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