Items 221 to 230 of 452 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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HEPES potassium salt | 82207-62-3 | sc-286007 sc-286007A sc-286007B | 25 g 100 g 250 g | $67.00 $190.00 $368.00 | ||
HEPES potassium salt is a buffering agent that maintains pH stability in biological systems, crucial for enzyme activity and cellular processes. Its zwitterionic structure allows for effective ionic interactions, enhancing solubility in aqueous environments. The compound exhibits unique hydrogen bonding capabilities, which can influence molecular interactions in biochemical assays. Additionally, its low toxicity and minimal interference with biological reactions make it an ideal choice for various laboratory applications. | ||||||
Tris Acetate-EDTA buffer | sc-296645 | 1 L | $19.00 | |||
Tris Acetate-EDTA buffer is a versatile solution that excels in maintaining pH stability and chelating metal ions, which is crucial for preserving the integrity of nucleic acids. Its unique buffering capacity arises from the interplay between its components, allowing for effective control of enzymatic reactions. The buffer's low ionic strength minimizes non-specific interactions, promoting accurate results in biochemical assays and molecular biology applications. | ||||||
Bromoacetic acid | 79-08-3 | sc-210962 sc-210962A | 100 g 500 g | $40.00 $100.00 | ||
Bromoacetic acid is a halogenated carboxylic acid characterized by its reactivity due to the presence of a bromine atom, which enhances electrophilicity. This compound readily participates in nucleophilic substitution reactions, making it a valuable intermediate in organic synthesis. Its ability to form stable complexes with metal ions can influence reaction pathways and kinetics. Additionally, it exhibits unique solubility properties, facilitating its use in various solvent systems. | ||||||
Lithium hydroxide | 1310-65-2 | sc-211742 | 100 g | $90.00 | ||
Lithium hydroxide exhibits unique properties as a strong base, facilitating deprotonation reactions and enhancing nucleophilicity in organic synthesis. Its ionic nature allows for effective solvation in polar solvents, promoting rapid reaction kinetics. The compound can form stable complexes with carbon dioxide, influencing carbon capture processes. Additionally, its hygroscopic nature contributes to its role in moisture control, impacting various chemical equilibria in laboratory settings. | ||||||
Oxalic acid dihydrate | 6153-56-6 | sc-203171 sc-203171A sc-203171B | 100 g 500 g 2.5 kg | $44.00 $99.00 $418.00 | ||
Oxalic acid dihydrate is a versatile organic compound characterized by its ability to form strong hydrogen bonds due to its two carboxylic acid groups. This property enhances its solubility in water and facilitates complexation with metal ions, making it useful in various analytical techniques. Its reactivity as a reducing agent allows it to participate in redox reactions, influencing reaction kinetics and pathways. Additionally, its crystalline structure contributes to its stability and ease of handling in laboratory environments. | ||||||
Lipoprotein Refolding Buffer | sc-295364 sc-295364A | 10 ml 50 ml | $40.00 $148.00 | |||
Lipoprotein Refolding Buffer is a specialized solution designed to facilitate the proper folding of proteins, particularly lipoproteins. Its unique composition promotes hydrophobic interactions, stabilizing protein structures during refolding processes. The buffer's tailored ionic environment enhances molecular chaperone activity, optimizing the kinetics of protein assembly. Additionally, its ability to maintain a consistent osmotic balance aids in preserving protein integrity, making it essential for studying complex biomolecular interactions. | ||||||
Aniline | 62-53-3 | sc-202952 sc-202952A sc-202952B | 5 g 100 g 500 g | $26.00 $32.00 $72.00 | 2 | |
Aniline is a versatile aromatic amine known for its ability to participate in electrophilic aromatic substitution reactions, making it a key player in organic synthesis. Its electron-donating amino group enhances nucleophilicity, facilitating interactions with electrophiles. Aniline's solubility in organic solvents and its capacity to form stable complexes with metal ions further underscore its utility in various chemical pathways. Additionally, its reactivity with isocyanates and acyl chlorides highlights its role in forming diverse derivatives. | ||||||
Sodium oxalate | 62-76-0 | sc-203396 sc-203396A | 100 g 500 g | $42.00 $136.00 | 5 | |
Sodium oxalate is a versatile compound known for its ability to act as a chelating agent, forming stable complexes with metal ions. This property facilitates its use in various analytical techniques, particularly in titrations and as a standard in gravimetric analysis. Its crystalline structure contributes to its solubility characteristics, influencing reaction rates and pathways. Additionally, sodium oxalate can participate in redox reactions, showcasing its role in complexation and ion exchange processes in laboratory settings. | ||||||
Cibacron Blue Agarose | sc-294028 sc-294028A | 1 ml 10 ml | $35.00 $150.00 | 3 | ||
Cibacron Blue Agarose is a specialized dye-labeled agarose that exhibits strong affinity for various biomolecules through hydrophobic and ionic interactions. Its unique structure allows for selective binding, facilitating the separation of proteins and nucleic acids. The dye's stability and resistance to photobleaching enhance its performance in chromatographic applications. Additionally, its high porosity and low nonspecific binding properties contribute to efficient purification processes, ensuring high-resolution results. | ||||||
Benzoic acid | 65-85-0 | sc-203317 sc-203317A sc-203317B | 25 g 100 g 500 g | $20.00 $50.00 $60.00 | ||
Benzoic acid is a versatile compound known for its ability to form hydrogen bonds, which significantly influences its solubility and reactivity in various solvents. As a weak acid, it participates in proton transfer reactions, showcasing distinct kinetic profiles in esterification and acid-base reactions. Its aromatic structure allows for π-π stacking interactions, affecting its behavior in complexation and crystallization processes. This unique molecular behavior makes it a valuable tool in studying reaction mechanisms and thermodynamic properties. |