Description
2-Amino-6-chloro-9-(2'-deoxy-b-D-ribofuranosyl)purine is a halogenated deoxynucleoside analogue with CAS number 120595-72-4, empirical formula C₁₀H₁₂ClN₅O₃ and a molar mass of 285,69 g/mol. The 2-amino-6-chloro substitution pattern on the purine ring, combined with the 2'-deoxy-b-D-ribofuranosyl sugar, makes this compound of interest for nucleoside chemistry, intermediate synthesis and specialised biochemical studies. Documented molecular formula and molar mass support precise dosing and traceable documentation in experimental protocols. Research groups in organic synthesis, medicinal chemistry and nucleic-acid related work can use this material when preparing further derivatives or evaluating structure-dependent behaviour. Clear identity data and a compact pack format help laboratories maintain efficient, catalogue-driven supply of this defined purine deoxynucleoside building block.
This article is part of Fluorescent dyes & labels, in Dyes, stains & indicators.
Key features
- Purity (HPLC): ≥ 97 %
- Colour: white to off-white
- Form: powder to crystalline powder
- ¹H-NMR Spectrum: corresponds to assigned structure
- CAS number: 120595-72-4
- Pack sizes: 250 mg, 500 mg, 1 g
- Empirical formula: C₁₀H₁₂ClN₅O₃
- Molar mass: 285,69 g/mol
- Storage temperature: -20 °C
- Product group: Biochemicals
- Technical Information Sheet:
- Safety Data Sheet:
Compliance & Safety Information
Warning
Hazard Statements (H-Phrases)
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Questions about 2-Amino-6-chloro-9-(2'-deoxy-b-D-ribofur, anosyl)purine, 250 mg
What is this article?
2-Amino-6-chloro-9-(2'-deoxy-b-D-ribofur, anosyl)purine, 250 mg is the article on this page. Luminix Health distributes Carl Roth for laboratory use. It sits in Fluorescent dyes & labels, inside Dyes, stains & indicators, in Lab chemicals.
A fluorescent dye absorbs at one wavelength and emits at a longer one. As a label it is attached to a protein, a nucleic acid or a cell. Excitation and emission maxima, and the reactive group if it must conjugate, are the specification. The colour name does not tell you the wavelengths.
A dye or a stain binds, or changes colour, so that something invisible becomes visible. An indicator changes at a pH or a redox point. A fluorescent dye absorbs one wavelength and emits another, which is how a microscope or a plate reader picks it out. The excitation and emission, or the transition interval, are the specification. The colour name on the label is not. Structures are on PubChem under IUPAC names. Methods are in the PubMed literature.
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