Items 171 to 180 of 222 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Sabinene hydrate | 546-79-2 | sc-236845 sc-236845A | 500 mg 5 g | $43.00 $242.00 | ||
Sabinene hydrate is an important analytical standard known for its distinctive molecular interactions and reactivity patterns. As a cyclic monoterpene, it participates in various reaction pathways, including electrophilic additions and rearrangements. Its unique stereochemistry contributes to specific binding affinities with certain analytes, enhancing selectivity in analytical techniques. Furthermore, its volatility and solubility characteristics facilitate effective extraction and purification processes, making it a valuable tool in analytical applications. | ||||||
2-Hexanone | 591-78-6 | sc-238063 sc-238063A | 10 g 50 g | $35.00 $127.00 | ||
2-Hexanone serves as a crucial analytical standard, characterized by its unique carbonyl group that engages in hydrogen bonding and dipole-dipole interactions. This ketone exhibits distinct reactivity in oxidation and reduction pathways, influencing reaction kinetics and product formation. Its moderate volatility and solubility in organic solvents enhance its utility in chromatographic techniques, allowing for precise quantification and identification of compounds in complex mixtures. | ||||||
3,3′-Dichlorobenzidine dihydrochloride | 612-83-9 | sc-256572 | 25 g | $67.00 | ||
3,3'-Dichlorobenzidine dihydrochloride is a notable analytical standard, distinguished by its dual chlorine substituents that enhance its electron-withdrawing properties. This compound exhibits strong interactions with polar solvents, facilitating solubility and stability in various analytical methods. Its unique structure allows for selective reactivity in electrophilic aromatic substitution reactions, making it valuable for studying reaction mechanisms and kinetics in complex chemical environments. | ||||||
(±)-5-Dodecanolide | 713-95-1 | sc-239040 sc-239040A | 5 ml 100 ml | $36.00 $82.00 | ||
(±)-5-Dodecanolide serves as a significant analytical standard, characterized by its cyclic ester structure that influences its reactivity and solubility. This compound exhibits unique interactions with hydrophobic environments, enhancing its partitioning behavior in chromatographic techniques. Its ability to undergo ring-opening reactions under specific conditions allows for the exploration of reaction pathways and kinetics, making it a useful tool in the study of esterification processes and molecular dynamics. | ||||||
Nifenazone | 2139-47-1 | sc-236175 | 100 mg | $235.00 | ||
Nifenazone, as an analytical standard, is notable for its distinctive electronic properties and reactivity patterns. Its structure facilitates specific interactions with various solvents, influencing its solubility and stability in analytical applications. The compound's ability to participate in nucleophilic substitution reactions highlights its role in studying reaction kinetics and mechanisms. Additionally, Nifenazone's unique spectral characteristics make it valuable for calibration in spectroscopic analyses. | ||||||
(+)-Terpinen-4-ol | 2438-10-0 | sc-253625 | 1 ml | $146.00 | ||
(+)-Terpinen-4-ol serves as a crucial analytical standard, characterized by its unique hydrogen bonding capabilities and polar functional groups. These features enhance its solubility in various organic solvents, making it suitable for diverse analytical techniques. Its distinct chiral nature allows for the exploration of stereochemical interactions, while its reactivity in oxidation and reduction pathways provides insights into reaction dynamics. The compound's specific spectral fingerprints facilitate accurate identification and quantification in chromatographic methods. | ||||||
o-Fluoro-DL-phenylalanine | 2629-55-2 | sc-255399 | 5 g | $150.00 | ||
o-Fluoro-DL-phenylalanine is an important analytical standard, notable for its unique fluorine substitution that influences its electronic properties and reactivity. This modification enhances its interaction with polar solvents, improving solubility and stability in various analytical environments. The compound's ability to participate in specific hydrogen bonding interactions allows for detailed studies of molecular dynamics. Its distinct spectral characteristics enable precise identification in spectroscopic analyses, making it a valuable tool for researchers. | ||||||
Patent Blue V calcium salt | 3536-49-0 | sc-296025 sc-296025A | 10 g 25 g | $72.00 $109.00 | ||
Patent Blue V calcium salt serves as a critical analytical standard, distinguished by its unique dye properties and strong affinity for certain metal ions. Its vibrant color and stability in various pH environments facilitate precise colorimetric analyses. The compound exhibits specific interactions with proteins and other biomolecules, allowing for the exploration of binding kinetics and reaction pathways. Its distinct spectral features enhance detection sensitivity in analytical techniques, making it an essential reference material. | ||||||
cis-Nonachlor | 5103-73-1 | sc-257253 | 10 mg | $96.00 | ||
Cis-Nonachlor is a notable analytical standard characterized by its complex molecular structure and unique hydrophobic interactions. This compound exhibits distinct partitioning behavior in various solvents, influencing its solubility and extraction efficiency. Its stability under diverse environmental conditions allows for reliable quantification in analytical assays. Additionally, cis-Nonachlor's specific binding affinities with lipid membranes provide insights into its behavior in complex matrices, enhancing the understanding of its environmental persistence and bioaccumulation pathways. | ||||||
Poly(butyl methacrylate) | 9003-63-8 | sc-253287 sc-253287A | 5 g 250 g | $67.00 $146.00 | ||
Poly(butyl methacrylate) serves as a versatile analytical standard, distinguished by its robust polymeric structure and unique viscoelastic properties. This compound exhibits significant adhesion and compatibility with various substrates, facilitating effective surface interactions. Its molecular architecture allows for tailored modification, influencing reaction kinetics and polymerization pathways. Additionally, the material's thermal stability and resistance to chemical degradation enhance its reliability in analytical applications, making it a valuable tool for studying polymer behavior in diverse environments. | ||||||