Items 301 to 310 of 426 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
DAU 5884 hydrochloride | 131780-47-7 | sc-203912 sc-203912A | 10 mg 50 mg | $165.00 $693.00 | ||
DAU 5884 hydrochloride, as a salt, showcases intriguing electrostatic interactions that enhance its solubility in various solvents. Its unique molecular architecture facilitates specific coordination with metal ions, influencing its reactivity and stability in diverse chemical environments. The compound's ability to engage in hydrogen bonding and dipole-dipole interactions further modulates its physical properties, affecting its behavior in complex mixtures and reaction pathways. | ||||||
H-L-beta-HPhe-OH*HCl | 138165-77-2 | sc-285959 sc-285959A sc-285959B | 1 g 5 g 500 mg | $1170.00 $3640.00 $640.00 | ||
H-L-beta-HPhe-OH*HCl, as a salt, exhibits remarkable ionic characteristics that contribute to its stability in aqueous solutions. The presence of chloride ions enhances its dissociation, promoting effective ion pairing and solvation dynamics. This compound's unique stereochemistry allows for selective interactions with polar solvents, influencing its reactivity in various chemical processes. Additionally, its capacity for forming transient complexes can alter reaction kinetics, making it a subject of interest in studies of molecular behavior. | ||||||
Disodium Cycloheptylaminomethylene diphosphonate | 138330-18-4 | sc-204731 sc-204731A sc-204731B | 25 mg 100 mg 250 mg | $115.00 $250.00 $475.00 | ||
Disodium Cycloheptylaminomethylene diphosphonate, as a salt, showcases intriguing chelation properties due to its diphosphonate groups, which can form stable complexes with metal ions. This compound exhibits strong ionic interactions that enhance its solubility in polar solvents, facilitating unique reaction pathways. Its structural conformation allows for specific molecular recognition, influencing its reactivity and stability in various chemical environments, making it a fascinating subject for further exploration in coordination chemistry. | ||||||
BD 1008 Dihydrobromide | 138356-09-9 | sc-207316 | 10 mg | $140.00 | ||
BD 1008 Dihydrobromide, as a salt, demonstrates notable ionic characteristics that contribute to its solubility and reactivity. The presence of bromide ions enhances its ability to participate in nucleophilic substitution reactions, facilitating distinct pathways in organic synthesis. Its crystalline structure allows for specific lattice interactions, influencing the kinetics of dissolution and reactivity. This compound's unique properties make it an interesting candidate for studies in salt behavior and ionic interactions. | ||||||
Chaetomellic acid A | 148796-51-4 | sc-221420 sc-221420A | 5 mg 25 mg | $47.00 $250.00 | 1 | |
Chaetomellic acid A, in its salt form, exhibits intriguing electrostatic interactions that enhance its solubility in polar solvents. The presence of its anionic component promotes unique hydrogen bonding capabilities, influencing its reactivity in various chemical environments. This compound's crystalline arrangement contributes to its stability and affects the kinetics of ion exchange processes, making it a subject of interest for exploring ionic dynamics and solvation phenomena. | ||||||
RS 23597-190 hydrochloride | 149719-06-2 | sc-203243 | 5 mg | $500.00 | ||
RS 23597-190 hydrochloride, as a salt, showcases distinctive ionic interactions that facilitate its dissolution in aqueous media. The chloride ion enhances its reactivity by participating in coordination complexes, influencing the compound's behavior in various chemical reactions. Its solid-state structure reveals a layered arrangement, which can affect diffusion rates and ion mobility, making it a compelling candidate for studies on ionic conductivity and phase transitions. | ||||||
Sodium 2-(4-methoxyphenoxy)propanoic acid | 150436-68-3 | sc-334853 sc-334853A | 10 g 50 g | $112.00 $439.00 | 1 | |
Sodium 2-(4-methoxyphenoxy)propanoic acid, as a salt, exhibits unique solubility characteristics due to its polar functional groups, promoting strong hydrogen bonding in solution. This compound's anionic and cationic components engage in dynamic electrostatic interactions, which can influence reaction kinetics and stability. Its crystalline form may display anisotropic properties, affecting how it interacts with light and heat, making it an interesting subject for material science investigations. | ||||||
Iron(III) Oxalate Hexahydrate | 166897-40-1 | sc-257624 | 100 g | $487.00 | ||
Iron(III) Oxalate Hexahydrate, as a salt, showcases intriguing coordination chemistry due to its ability to form complexes with various ligands. The presence of oxalate ions facilitates chelation, enhancing stability and influencing redox behavior. Its hydrated structure contributes to unique thermal properties, while the crystalline arrangement can lead to distinct optical characteristics. This compound's interactions in solution can also affect precipitation dynamics and solubility profiles, making it a subject of interest in various chemical studies. | ||||||
SB 224289 hydrochloride | 180084-26-8 (free acid) | sc-361336 sc-361336A sc-361336B sc-361336C | 10 mg 50 mg 250 mg 5 mg | $140.00 $351.00 $902.00 $78.00 | ||
SB 224289 hydrochloride, as a salt, exhibits notable solubility characteristics that enhance its reactivity in aqueous environments. Its ionic nature promotes strong electrostatic interactions, facilitating the formation of transient complexes with polar solvents. The compound's unique structural arrangement allows for specific hydrogen bonding patterns, influencing its stability and reactivity. Additionally, its behavior in solution can alter ionic strength, impacting reaction kinetics and equilibrium dynamics in various chemical systems. | ||||||
YM-53601 | 182959-33-7 | sc-205543 sc-205543A | 500 µg 1 mg | $336.00 $480.00 | 3 | |
YM-53601, in its salt form, demonstrates distinctive solvation properties that significantly influence its reactivity. The compound's ionic structure fosters robust interactions with surrounding molecules, enhancing its ability to participate in complexation reactions. Its unique arrangement allows for specific coordination with metal ions, potentially altering catalytic pathways. Furthermore, the salt's high ionic mobility contributes to rapid diffusion in solution, affecting reaction rates and equilibria in diverse chemical contexts. | ||||||