Analytical Standards
Items 101 to 110 of 221 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Hydrochlorothiazide | 58-93-5 | sc-207738 sc-207738A sc-207738B sc-207738C sc-207738D | 5 g 25 g 50 g 100 g 250 g | $55.00 $240.00 $333.00 $562.00 $988.00 | ||
Hydrochlorothiazide, as an analytical standard, is notable for its ability to form hydrogen bonds, which enhances its solubility in aqueous solutions. This compound exhibits unique spectroscopic properties, making it suitable for UV-Vis and HPLC analyses. Its distinct ionization behavior allows for precise detection and quantification in complex matrices. Furthermore, its stability under varying pH conditions ensures consistent performance in analytical methodologies, facilitating reliable results across diverse applications. | ||||||
2-Phenethylamine | 64-04-0 | sc-238192 | 50 ml | $47.00 | ||
2-Phenethylamine serves as a valuable analytical standard due to its ability to engage in π-π stacking interactions, which can influence its behavior in chromatographic separations. This compound exhibits notable fluorescence properties, enhancing its detectability in various analytical techniques. Its unique reactivity with electrophiles allows for the formation of stable derivatives, aiding in the identification and quantification of related compounds in complex samples. | ||||||
Dienestrol | 84-17-3 | sc-239717 | 100 mg | $73.00 | ||
Dienestrol is an analytical standard characterized by its ability to form hydrogen bonds, which can significantly affect its solubility and partitioning behavior in various solvents. This compound exhibits distinct UV absorbance characteristics, making it suitable for spectrophotometric analysis. Its stereochemistry contributes to unique interactions in chiral environments, facilitating the study of enantiomeric separations and enhancing the understanding of molecular recognition processes. | ||||||
DL-Mandelic acid | 90-64-2 | sc-239828 | 100 g | $40.00 | ||
DL-Mandelic acid serves as an analytical standard notable for its capacity to engage in specific molecular interactions, particularly through hydrogen bonding and dipole-dipole interactions. Its unique stereochemical configuration allows for selective reactivity in various chemical environments, influencing reaction kinetics and pathways. Additionally, its solubility profile in polar and non-polar solvents aids in the development of analytical methods, enhancing the precision of quantitative analyses. | ||||||
Chlorpropamide | 94-20-2 | sc-234350 | 25 g | $73.00 | 7 | |
Chlorpropamide, as an analytical standard, exhibits distinctive properties that facilitate its role in various analytical techniques. Its ability to form stable complexes through coordination with metal ions enhances its utility in spectroscopic analyses. The compound's hydrophobic character influences its partitioning behavior in chromatographic systems, allowing for effective separation. Furthermore, its reactivity with nucleophiles can be leveraged to study reaction mechanisms and kinetics in diverse chemical environments. | ||||||
1,3-Dinitrobenzene | 99-65-0 | sc-237732 sc-237732A | 25 g 100 g | $52.00 $104.00 | ||
1,3-Dinitrobenzene serves as a crucial analytical standard due to its unique electronic structure, which allows for selective interactions with various reagents. Its nitro groups enhance electron-withdrawing capabilities, influencing reaction rates and pathways in electrophilic aromatic substitution. The compound's distinct UV-Vis absorption characteristics enable precise quantification in spectrophotometric analyses. Additionally, its stability under various conditions makes it a reliable reference for calibration in analytical methodologies. | ||||||
Coumafuryl | 117-52-2 | sc-223901 | 10 mg | $140.00 | ||
Coumafuryl is an analytical standard notable for its unique reactivity and interaction with nucleophiles, which facilitates the study of reaction mechanisms in organic synthesis. Its structure promotes specific hydrogen bonding and π-π stacking interactions, influencing solubility and partitioning behavior in various solvents. The compound's distinct spectral properties, particularly in the UV region, allow for effective monitoring in chromatographic techniques, enhancing its utility in analytical applications. | ||||||
Acetylacetone | 123-54-6 | sc-239193 sc-239193A | 100 ml 500 ml | $39.00 $64.00 | ||
Acetylacetone serves as an analytical standard characterized by its ability to form chelates with metal ions, enhancing its role in coordination chemistry studies. Its diketone structure enables strong intramolecular hydrogen bonding, which influences its stability and reactivity. The compound exhibits distinct UV-Vis absorption characteristics, making it suitable for spectrophotometric analysis. Additionally, its volatility and solubility in various organic solvents facilitate diverse analytical methodologies. | ||||||
Hydroflumethiazide | 135-09-1 | sc-211601 | 100 mg | $250.00 | ||
Hydroflumethiazide is an analytical standard notable for its unique interactions with anions and cations, which can influence ion exchange processes. Its thiazide structure allows for specific hydrogen bonding and dipole-dipole interactions, affecting solubility and reactivity in various solvents. The compound's distinct UV-Vis spectral profile aids in quantitative analysis, while its stability under varying pH conditions makes it a reliable reference in analytical chemistry. | ||||||
Amprolium HCl | 137-88-2 | sc-391655 sc-391655A | 25 g 100 g | $84.00 $260.00 | 1 | |
Amprolium HCl serves as an analytical standard characterized by its ability to form stable complexes with metal ions, enhancing its role in coordination chemistry. Its unique structure facilitates specific electrostatic interactions, influencing solubility and reactivity in diverse environments. The compound exhibits distinct chromatographic behavior, making it valuable for separation techniques. Additionally, its spectral properties allow for precise detection and quantification in analytical applications. | ||||||