Bases
Items 41 to 45 of 45 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
9-Methoxymethyl Guanine | 1202645-50-8 | sc-484469 sc-484469A | 100 mg 1 g | $340.00 $2400.00 | ||
9-Methoxymethyl Guanine exhibits intriguing properties as a nucleobase, particularly through its ability to form hydrogen bonds, which are crucial for base pairing in nucleic acid structures. The presence of the methoxymethyl group enhances its steric profile, influencing molecular recognition and binding affinity. Additionally, its electron-rich nature facilitates nucleophilic attack in biochemical pathways, while its conformational adaptability allows for diverse interactions with other biomolecules, impacting stability and reactivity. | ||||||
Basic Red 12 | 6320-14-5 | sc-493223 | 5 g | $209.00 | ||
Basic Red 12 is characterized by its vibrant color and strong affinity for electron-rich sites, which enhances its ability to form hydrogen bonds and engage in π-π stacking interactions. This dye exhibits notable solubility in polar solvents, facilitating rapid diffusion in various media. Its cationic nature allows for effective adsorption onto negatively charged surfaces, influencing its behavior in dyeing processes and environmental applications. The compound's stability under varying pH conditions further underscores its versatility in diverse chemical environments. | ||||||
Adenosine-13C5 | 159496-13-6 | sc-478892 sc-478892A sc-478892B sc-478892C | 2.5 mg 25 mg 100 mg 250 mg | $286.00 $408.00 $1492.00 $1958.00 | ||
Adenosine-13C5 is a unique isotopically labeled nucleoside that facilitates advanced studies in biochemical dynamics. Its carbon-13 labeling allows for enhanced resolution in mass spectrometry, enabling precise tracking of metabolic fluxes. The compound's distinct isotopic signature can influence reaction kinetics, providing insights into enzyme mechanisms and substrate specificity. Additionally, it plays a role in elucidating the structural dynamics of nucleic acids, contributing to a deeper understanding of molecular interactions within cellular systems. | ||||||
Ammonia | 7664-41-7 | sc-359914A sc-359914 | 100 ml 800 ml | $107.00 $280.00 | ||
Ammonia is a weak base characterized by its ability to accept protons, forming ammonium ions in aqueous solutions. Its electron-rich nitrogen atom enhances its nucleophilic properties, enabling it to participate in diverse chemical reactions, including alkylation and acylation. The molecule's geometry allows for effective overlap of orbitals, promoting reaction kinetics. Furthermore, ammonia's affinity for hydrogen bonding contributes to its unique interactions with various substrates, influencing reaction pathways and equilibria. | ||||||
Queuine hydrochloride | 85549-16-2 | sc-394021 sc-394021-CW sc-394021A sc-394021B sc-394021C sc-394021D sc-394021D-CW | 500 µg 500 µg 5 mg 50 mg 100 mg 500 mg 500 mg | $510.00 $663.00 $4600.00 $40300.00 $64576.00 $69370.00 $69370.00 | 2 | |
Queuine hydrochloride functions as a unique base, characterized by its ability to engage in specific molecular interactions that enhance its reactivity. It can participate in proton transfer reactions, facilitating the formation of stable intermediates. The compound's distinct electronic structure allows it to stabilize charged species, promoting efficient reaction pathways. Its solubility in polar solvents further aids in achieving rapid kinetics, making it an intriguing subject for studying base-catalyzed transformations. | ||||||