Items 61 to 70 of 222 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Rhamnetin | 90-19-7 | sc-236668 | 1 mg | $83.00 | ||
Rhamnetin serves as an analytical standard notable for its distinctive flavonoid structure, which enables specific interactions with metal ions and proteins, aiding in the study of complex biochemical pathways. Its solubility in polar solvents allows for effective extraction and quantification in various matrices. Furthermore, Rhamnetin's antioxidant properties contribute to its role in assessing oxidative stress markers, making it a valuable tool in analytical chemistry for environmental and food safety studies. | ||||||
4-Nonylphenol | 104-40-5 | sc-256816 sc-256816A | 100 mg 5 g | $67.00 $401.00 | 2 | |
4-Nonylphenol is an analytical standard characterized by its hydrophobic nature and ability to form stable complexes with various organic compounds. Its unique alkyl chain enhances its partitioning behavior in chromatographic techniques, facilitating the separation and identification of environmental pollutants. Additionally, 4-Nonylphenol exhibits significant interactions with biological membranes, making it a critical compound for studying endocrine disruption and environmental toxicity assessments. | ||||||
Sodium 4-hydroxybenzoate | 114-63-6 | sc-251002 sc-251002A | 25 g 50 g | $58.00 $96.00 | ||
Sodium 4-hydroxybenzoate serves as an analytical standard notable for its solubility in aqueous solutions and its role as a preservative in various formulations. Its ability to form hydrogen bonds enhances its reactivity in spectroscopic analyses, allowing for precise quantification in complex matrices. The compound's distinct pH-dependent behavior influences its stability and interaction with other analytes, making it essential for method development in analytical chemistry. | ||||||
Sennoside B | 128-57-4 | sc-258154 sc-258154A | 25 mg 500 mg | $159.00 $942.00 | ||
Sennoside B is an analytical standard characterized by its unique glycosidic structure, which facilitates specific interactions with various biological receptors. Its stability under diverse pH conditions allows for reliable detection in chromatographic methods. The compound exhibits distinct fluorescence properties, enhancing its utility in spectroscopic techniques. Additionally, its capacity to form stable complexes with metal ions can influence reaction kinetics, making it a valuable reference in analytical assessments. | ||||||
2,6-Pyridinedicarboxylic acid | 499-83-2 | sc-238430 sc-238430A sc-238430B sc-238430C | 5 g 100 g 1 kg 10 kg | $34.00 $94.00 $728.00 $6586.00 | ||
2,6-Pyridinedicarboxylic acid serves as a versatile analytical standard, notable for its ability to form hydrogen bonds and chelate metal ions, which can significantly alter reaction pathways. Its distinct carboxylic acid groups enhance solubility in polar solvents, facilitating accurate quantification in various analytical techniques. The compound's reactivity with amines and alcohols allows for the exploration of esterification and amidation processes, making it a key reference in studying reaction kinetics and mechanisms. | ||||||
Kinetin | 525-79-1 | sc-207780 sc-207780A | 1 g 5 g | $38.00 $48.00 | ||
Kinetin, a cytokinin derivative, is recognized for its role in modulating plant growth and development. As an analytical standard, it exhibits unique interactions with nucleic acids and proteins, influencing cellular signaling pathways. Its ability to stabilize reactive intermediates enhances the study of enzymatic reactions and metabolic processes. Kinetin's distinct solubility characteristics in various solvents facilitate precise analytical measurements, making it essential for investigating biochemical dynamics. | ||||||
β-Amyrin | 559-70-6 | sc-252376 | 10 mg | $520.00 | ||
β-Amyrin, a triterpene, serves as a crucial analytical standard due to its unique structural properties and interactions with lipid membranes. Its hydrophobic nature allows for the exploration of membrane fluidity and permeability, while its ability to form complexes with various biomolecules aids in understanding lipid-protein interactions. Additionally, β-Amyrin's distinct chromatographic behavior enhances separation techniques, providing insights into its role in natural product chemistry and metabolic pathways. | ||||||
Iohexol | 66108-95-0 | sc-205351 sc-205351A sc-205351B | 1 g 5 g 25 g | $54.00 $104.00 $214.00 | 1 | |
Iohexol, a non-ionic contrast agent, is utilized as an analytical standard due to its unique solubility characteristics and interactions with water molecules. Its hydrophilic properties facilitate the study of solvation dynamics and molecular diffusion in aqueous environments. Furthermore, Iohexol's distinct spectral features enable precise quantification in chromatographic analyses, making it a valuable tool for investigating complex mixtures and enhancing the understanding of molecular interactions in various analytical applications. | ||||||
Apigenin 7-glucoside | 578-74-5 | sc-233888 | 5 mg | $180.00 | 1 | |
Apigenin 7-glucoside serves as an analytical standard, notable for its specific binding interactions with various proteins and enzymes, which can influence reaction kinetics in biochemical assays. Its unique structural features allow for selective detection in chromatographic methods, enhancing the resolution of complex samples. Additionally, its stability under varying pH conditions makes it an ideal candidate for studying the effects of environmental factors on molecular behavior, providing insights into its role in diverse analytical contexts. | ||||||
Tris(pentafluorophenyl)borane | 1109-15-5 | sc-258317 | 1 g | $150.00 | ||
Tris(pentafluorophenyl)borane is an analytical standard distinguished by its strong Lewis acidity and unique electronic properties, which facilitate selective interactions with nucleophiles. Its highly fluorinated structure enhances solubility in nonpolar solvents, making it suitable for various analytical techniques. The compound exhibits distinct reactivity patterns, allowing for the exploration of reaction mechanisms and kinetics in organometallic chemistry, thereby providing valuable insights into molecular behavior in complex systems. | ||||||