Items 161 to 170 of 222 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Eleutheroside B | 118-34-3 | sc-285486 sc-285486A | 10 mg 20 mg | $373.00 $739.00 | ||
Eleutheroside B serves as an analytical standard notable for its complex glycosidic structure, which facilitates specific interactions with various receptors and enzymes. Its unique stereochemistry influences its solubility and partitioning in different solvents, enhancing its utility in chromatographic separations. The compound's capacity for forming stable complexes with metal ions can also affect reaction kinetics, making it a valuable reference in analytical chemistry for studying molecular interactions. | ||||||
Diethylstilbestrol dipropionate | 130-80-3 | sc-227859 | 1 g | $28.00 | ||
Diethylstilbestrol dipropionate is an analytical standard characterized by its unique dual aromatic structure, which allows for selective binding to estrogen receptors. This compound exhibits distinct hydrophobic properties, influencing its distribution in various media and enhancing its role in chromatographic techniques. Its ability to undergo specific conformational changes under varying conditions provides insights into molecular dynamics, making it a critical reference for studying ligand-receptor interactions and reaction mechanisms. | ||||||
1-Naphthylamine | 134-32-7 | sc-237593 | 25 g | $72.00 | ||
1-Naphthylamine serves as an analytical standard notable for its planar aromatic structure, which facilitates π-π stacking interactions and enhances its solubility in organic solvents. This compound exhibits distinct electron-donating properties, influencing its reactivity in electrophilic aromatic substitution reactions. Its stability under various conditions allows for reliable quantification in analytical methods, providing a benchmark for studying amine reactivity and environmental persistence. | ||||||
Benzyl acetate | 140-11-4 | sc-252427 | 100 g | $30.00 | 1 | |
Benzyl acetate is an analytical standard characterized by its ester functional group, which enables unique dipole-dipole interactions and contributes to its volatility. This compound exhibits distinct reactivity patterns in nucleophilic acyl substitution, making it a useful reference for studying ester hydrolysis kinetics. Its pleasant, fruity aroma aids in sensory analysis, while its solubility in various solvents allows for versatile applications in chromatographic techniques. | ||||||
Dibenzo[a,l]pyrene | 191-30-0 | sc-234559 | 100 mg | $970.00 | ||
Dibenzo[a,l]pyrene serves as an analytical standard notable for its polycyclic aromatic structure, which facilitates strong π-π stacking interactions and hydrophobic effects. This compound is particularly relevant in studies of environmental pollutants due to its stability and resistance to degradation. Its unique electronic properties influence reaction kinetics in photochemical processes, making it a critical reference for assessing the behavior of complex mixtures in analytical chemistry. | ||||||
Benzo[e]pyrene | 192-97-2 | sc-257135 | 25 mg | $541.00 | ||
Benzo[e]pyrene, an analytical standard, is characterized by its planar polycyclic structure, which enhances its ability to engage in π-π interactions and hydrogen bonding. This compound exhibits notable fluorescence properties, making it useful in spectroscopic analyses. Its stability under various conditions allows for reliable quantification in complex matrices, while its reactivity in oxidative pathways provides insights into environmental degradation processes, crucial for understanding pollutant behavior. | ||||||
Indeno[1,2,3-cd]pyrene | 193-39-5 | sc-257601 | 10 mg | $204.00 | ||
Indeno[1,2,3-cd]pyrene serves as a critical analytical standard due to its unique polycyclic aromatic structure, which facilitates strong π-π stacking interactions and enhances its adsorption properties. This compound exhibits distinct photophysical characteristics, including significant light absorption in the UV-visible range, making it suitable for advanced spectroscopic techniques. Its persistence in environmental samples allows for the study of its transformation pathways, contributing to a deeper understanding of polycyclic aromatic hydrocarbon behavior in various matrices. | ||||||
2-Thenoyltrifluoroacetone | 326-91-0 | sc-251801 | 5 g | $37.00 | 1 | |
2-Thenoyltrifluoroacetone is a versatile analytical standard characterized by its ability to form chelates with metal ions, enhancing its utility in complexometric titrations. Its trifluoromethyl group imparts unique electronic properties, influencing reaction kinetics and selectivity in various analytical methods. The compound exhibits notable solubility in organic solvents, facilitating its application in diverse analytical techniques, including chromatography and spectrophotometry, where it serves as a reliable reference for quantification. | ||||||
2,3-Butanedione | 431-03-8 | sc-238264 sc-238264A | 1 ml 5 ml | $35.00 $122.00 | ||
2,3-Butanedione is a key analytical standard known for its role in flavor and fragrance analysis due to its distinct carbonyl groups, which engage in hydrogen bonding and contribute to its reactivity. This diketone exhibits unique behavior in oxidation reactions, making it a valuable marker in studies of metabolic pathways. Its volatility and ability to participate in condensation reactions enhance its application in various analytical techniques, including gas chromatography and mass spectrometry. | ||||||
Diperodon hydrochloride | 537-12-2 | sc-234775 | 5 g | $54.00 | 1 | |
Diperodon hydrochloride serves as a crucial analytical standard, characterized by its unique interactions as an acid halide. Its reactivity is influenced by the presence of halogen atoms, which can facilitate nucleophilic substitution reactions. This compound exhibits distinct solubility properties, allowing for effective separation in chromatographic methods. Additionally, its ability to form stable complexes with various analytes enhances its utility in analytical chemistry, particularly in identifying and quantifying target compounds. | ||||||