Description
Naltrexone impurity A is an impurity reference material offered at a minimum purity of 95 % for pharmaceutical and analytical applications. The compound is registered under CAS number 1007856-83-8, has the empirical formula C₁₇H₁₇NO₅ and a molar mass of 315,32 g/mol. Physical data include a boiling point of 621,5 °C and a flash point of 329,7 °C. Laboratories performing HPLC or LC-MS work can employ the material for calibration, peak identification and system suitability testing within impurity control programmes. This biochemical standard from manufacturer Carl ROTH provides a clearly specified chemical identity and assay level for research and development environments. The compact pack supports reference collections, validation studies and routine monitoring of process or degradation impurities associated with naltrexone.
This article is part of Chromatography standards (GC, HPLC, pesticides), in Analytical standards & reference materials.
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Questions about Naltrexone, min. 95 %, impurity A, 1 mg
What is this article?
Naltrexone, min. 95 %, impurity A, 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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