Items 121 to 130 of 138 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Propionaldehyde O-pentafluorophenylmethyl-oxime | 932710-53-7 | sc-236479 sc-236479A | 10 mg 100 mg | $320.00 $2140.00 | ||
Propionaldehyde O-pentafluorophenylmethyl-oxime serves as a sophisticated chromatography reagent, distinguished by its oxime functional group that facilitates specific interactions with diverse analytes. The pentafluorophenyl moiety enhances the compound's polarity and hydrophobicity, optimizing retention times in chromatographic systems. Its unique steric configuration allows for selective binding, improving separation efficiency and enhancing detection limits, making it a valuable tool for complex mixture analysis. | ||||||
Acrolein O-pentafluorophenylmethyl-oxime | 932710-55-9 | sc-233816 | 10 mg | $135.00 | ||
Acrolein O-pentafluorophenylmethyl-oxime is a specialized chromatography reagent characterized by its unique oxime structure, which promotes selective interactions with target compounds. The presence of the pentafluorophenyl group significantly increases electron-withdrawing capacity, enhancing the reagent's reactivity and stability. This compound exhibits distinct solubility properties, allowing for improved phase separation and resolution in chromatographic applications, thereby facilitating the analysis of intricate mixtures with precision. | ||||||
A2B2-Ionophore | 1253421-84-9 | sc-396572 | 25 mg | $210.00 | ||
A2B2-Ionophore is a distinctive chromatography reagent known for its ability to form stable complexes with cations, enhancing selectivity in separation processes. Its unique ionophoric properties facilitate the transport of ions across membranes, influencing reaction kinetics and improving analyte retention. The compound's tailored hydrophobic and hydrophilic balance allows for effective partitioning in various chromatographic systems, optimizing resolution and sensitivity in complex sample analysis. | ||||||
Percoll® | sc-500790 sc-500790A | 25 ml 100 ml | $37.00 $88.00 | 8 | ||
Percoll® is a specialized chromatography reagent characterized by its unique density gradient formation, which enables efficient separation of particles based on size and density. Its colloidal silica matrix provides a stable environment for biomolecules, promoting enhanced resolution during centrifugation. The reagent's tunable viscosity and low osmotic pressure facilitate optimal flow dynamics, allowing for precise fractionation and improved recovery of target analytes in complex mixtures. | ||||||
Quizalofop-p-tefuryl solution | 200509-41-7 | sc-229031 | 2 ml | $131.00 | ||
Quizalofop-p-tefuryl solution serves as a versatile chromatography reagent, notable for its selective interaction with specific analytes through hydrophobic and electrostatic forces. Its unique structure allows for tailored retention times, enhancing separation efficiency. The reagent's stability under varying pH conditions ensures consistent performance, while its ability to form complexes with target compounds aids in the resolution of complex mixtures, optimizing analytical outcomes. | ||||||
(6R,7R)-7-amino-8-oxo-3-((Z)-prop-1-enyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid | 106447-44-3 | sc-337277 | 1 g | $500.00 | ||
(6R,7R)-7-amino-8-oxo-3-((Z)-prop-1-enyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid exhibits unique properties as a chromatography reagent, particularly through its ability to form complex interactions with various analytes. The bicyclic structure facilitates selective binding, enhancing separation efficiency. Its thiol group can participate in nucleophilic reactions, allowing for tailored modifications that improve chromatographic resolution and analyte retention. | ||||||
2-Acetamido-4-methyl-5-thiazolesulfonyl chloride | 69812-29-9 | sc-223346 | 1 g | $71.00 | ||
2-Acetamido-4-methyl-5-thiazolesulfonyl chloride is a specialized chromatography reagent that exhibits strong electrophilic characteristics, facilitating the derivatization of nucleophilic analytes. Its thiazole moiety enhances selectivity through π-π stacking interactions, while the sulfonyl chloride group promotes rapid acylation reactions. This reagent's ability to form stable adducts with various functional groups allows for improved resolution and sensitivity in complex sample matrices, making it a powerful tool in analytical chemistry. | ||||||
Neoxanthin | 14660-91-4 | sc-506409 | 1 mg | $1100.00 | ||
Neoxanthin, a carotenoid pigment, serves as a unique chromatography reagent due to its distinctive structural features and interactions. Its conjugated double bond system allows for strong π-π stacking, enhancing separation efficiency in chromatographic applications. The presence of specific functional groups facilitates hydrogen bonding, which can influence retention times. Additionally, its hydrophobic nature aids in partitioning during liquid chromatography, optimizing analyte resolution. | ||||||
1-Chlorobutane | 109-69-3 | sc-397740 | 200 ml | $68.00 | ||
1-Chlorobutane serves as an effective chromatography reagent, characterized by its ability to interact selectively with various analytes. The chlorine substituent introduces a polar functional group, enhancing its affinity for polar compounds while maintaining compatibility with non-polar substances. This duality allows for tailored separation processes. Additionally, its moderate volatility aids in the rapid elution of components, optimizing resolution and efficiency in chromatographic techniques. | ||||||
DEAE-Cellulose, preswollen | 9013-34-7 | sc-506208 sc-506208A | 100 g 500 g | $364.00 $733.00 | 1 | |
DEAE-Cellulose, preswollen, is a highly effective chromatography reagent characterized by its quaternary ammonium groups that facilitate strong ionic interactions with negatively charged biomolecules. This unique property enhances its selectivity in ion-exchange chromatography, allowing for efficient separation of proteins and nucleic acids. Its porous structure provides a large surface area, promoting rapid mass transfer and improved resolution during chromatographic processes. | ||||||