Analytical Standards
Items 121 to 130 of 223 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
2,4,6-Tris(pentafluoroethyl)-1,3,5-triazine | 858-46-8 | sc-251855 | 500 mg | $109.00 | ||
2,4,6-Tris(pentafluoroethyl)-1,3,5-triazine is an analytical standard notable for its highly electronegative pentafluoroethyl groups, which significantly influence its reactivity and stability. This compound exhibits unique interactions with polar solvents, enhancing its solubility and facilitating its role in chromatographic techniques. Its distinct electronic structure allows for selective binding in complexation reactions, making it a valuable tool for precise analytical measurements in various chemical assessments. | ||||||
(±)-α-Lipoamide | 940-69-2 | sc-239160A sc-239160 sc-239160B sc-239160C | 1 g 2.5 g 5 g 10 g | $260.00 $270.00 $520.00 $843.00 | 2 | |
(±)-α-Lipoamide serves as an analytical standard characterized by its ability to form stable complexes with metal ions, enhancing its utility in various analytical techniques. Its unique thiol and amide functional groups facilitate specific interactions with biomolecules, allowing for the study of enzyme kinetics and metabolic pathways. The compound's redox properties enable it to participate in electron transfer reactions, making it a versatile reference in analytical chemistry for assessing reaction dynamics. | ||||||
Acetohexamide | 968-81-0 | sc-254935 | 1 g | $52.00 | ||
Acetohexamide is an analytical standard notable for its ability to engage in hydrogen bonding and dipole-dipole interactions, which influence its solubility and reactivity in various solvents. Its unique structure allows for selective interactions with specific receptors, aiding in the study of molecular recognition processes. Additionally, the compound's stability under varying pH conditions makes it a reliable reference for assessing reaction kinetics and mechanistic pathways in analytical applications. | ||||||
Borax Anhydrous | 1330-43-4 | sc-239405 sc-239405A | 100 g 500 g | $119.00 $457.00 | ||
Borax Anhydrous serves as a crucial analytical standard, characterized by its ability to form complexation interactions with metal ions, enhancing its role in various analytical techniques. Its unique lattice structure contributes to its solubility behavior, influencing reaction dynamics in solution. The compound's hygroscopic nature allows it to absorb moisture, which can affect its reactivity and stability, making it essential for precise calibration in analytical methodologies. | ||||||
Decachlorobiphenyl | 2051-24-3 | sc-257302 | 10 mg | $89.00 | ||
Decachlorobiphenyl is a highly chlorinated biphenyl compound that serves as an analytical standard, notable for its stability and resistance to degradation. Its extensive halogenation alters its electronic properties, affecting interactions with various solvents and matrices. This compound exhibits unique adsorption characteristics, influencing its behavior in chromatographic techniques. Additionally, its hydrophobic nature impacts partitioning in environmental studies, making it a key reference for assessing polychlorinated biphenyls in analytical applications. | ||||||
(+)-Menthone | 3391-87-5 | sc-228448 | 1 ml | $275.00 | ||
(+)-Menthone is a chiral monoterpene ketone that serves as an analytical standard, distinguished by its unique stereochemistry and odor profile. Its molecular interactions are influenced by hydrogen bonding and dipole-dipole interactions, which can affect solubility and volatility in various solvents. The compound's distinct pathways in gas chromatography highlight its utility in separating enantiomers, while its reactivity in oxidation and reduction reactions provides insights into ketone behavior in analytical chemistry. | ||||||
BDE No 47 solution | 5436-43-1 | sc-233922 | 1 ml | $306.00 | ||
BDE No 47 solution is a brominated flame retardant that functions as an analytical standard, characterized by its complex molecular interactions and stability under various conditions. Its unique structure allows for specific binding affinities with various substrates, influencing its behavior in chromatographic separations. The compound exhibits distinct reaction kinetics, particularly in oxidative environments, making it a valuable reference for studying environmental persistence and degradation pathways in analytical applications. | ||||||
Barium citrate tribasic heptahydrate | 6487-29-2 | sc-239270 | 25 g | $107.00 | ||
Barium citrate tribasic heptahydrate serves as a crucial analytical standard, notable for its unique solubility properties and crystalline structure. Its ability to form stable complexes with various ions enhances its utility in ion-selective analyses. The compound exhibits distinct thermal stability and hygroscopic behavior, influencing its reactivity in different environments. These characteristics make it an essential reference for studying ionic interactions and solvation dynamics in analytical chemistry. | ||||||
Peonidin 3-O-glucoside chloride | 6906-39-4 | sc-236333 | 1 mg | $412.00 | ||
Peonidin 3-O-glucoside chloride is an important analytical standard recognized for its unique chromophoric properties, which facilitate precise spectroscopic analysis. Its capacity to engage in specific hydrogen bonding interactions enhances its stability in solution, making it a reliable reference for studying flavonoid behavior. Additionally, its distinct reactivity in redox processes allows for the exploration of electron transfer mechanisms, providing insights into complex biochemical pathways. | ||||||
2-Chloro-5,5-dimethyl-1,3-cyclohexanedione | 7298-89-7 | sc-356413 sc-356413A | 250 mg 1 g | $116.00 $300.00 | ||
2-Chloro-5,5-dimethyl-1,3-cyclohexanedione serves as a crucial analytical standard due to its distinctive reactivity patterns and ability to form stable complexes with various metal ions. Its unique steric configuration influences reaction kinetics, allowing for selective interactions in complex mixtures. The compound's propensity for nucleophilic attack and its role in condensation reactions make it a valuable tool for investigating reaction mechanisms and understanding molecular dynamics in analytical chemistry. | ||||||