Items 191 to 200 of 223 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Benzyl Orange | 36402-77-4 | sc-291956 sc-291956A | 1 g 5 g | $116.00 $495.00 | ||
Benzyl Orange is a sulfonic acid dye that exhibits unique chromogenic properties, making it an effective analytical standard. Its distinct structural features enable selective interactions with various analytes, facilitating colorimetric detection. The compound undergoes protonation and deprotonation, influencing its absorbance characteristics across different pH levels. This behavior allows for precise monitoring of reaction kinetics and enhances its utility in titrations and spectrophotometric analyses. | ||||||
trans-Nonachlor | 39765-80-5 | sc-258274 | 25 mg | $165.00 | ||
trans-Nonachlor is a chlorinated hydrocarbon that serves as a valuable analytical standard due to its unique hydrophobic interactions and stability in various solvents. Its complex molecular structure allows for specific binding with lipophilic compounds, enhancing its role in environmental monitoring. The compound's persistence and resistance to degradation make it ideal for studying degradation pathways and assessing bioaccumulation in ecological studies. | ||||||
Fenvalerate | 51630-58-1 | sc-24014 sc-24014A | 25 mg 100 mg | $78.00 $226.00 | 2 | |
Fenvalerate is a synthetic pyrethroid characterized by its selective action on insect sodium channels, leading to neurotoxic effects in target species. As an analytical standard, it exhibits distinct partitioning behavior in various matrices, facilitating the study of its environmental fate. Its stereochemistry influences interaction kinetics, making it a key compound for investigating metabolic pathways and degradation processes in ecological assessments. | ||||||
Oxeladin citrate salt | 52432-72-1 | sc-236262 | 25 g | $49.00 | ||
Oxeladin citrate salt serves as a valuable analytical standard, notable for its unique solubility characteristics and stability in diverse solvents. Its interactions with specific receptors can be studied through chromatographic techniques, revealing insights into its behavior in complex mixtures. The compound's distinct ionization properties allow for precise quantification in analytical assays, making it essential for exploring reaction mechanisms and environmental persistence in various analytical contexts. | ||||||
Super-DHB | 63542-76-7 | sc-236958 | 1 g | $102.00 | ||
Super-DHB is an analytical standard distinguished by its unique reactivity as an acid halide, facilitating specific acylation reactions. Its ability to form stable adducts with nucleophiles enables detailed studies of reaction kinetics and mechanistic pathways. The compound's selective interactions with various functional groups enhance its utility in synthetic chemistry, while its distinct spectral properties allow for effective monitoring in analytical techniques, providing insights into molecular behavior in diverse environments. | ||||||
Amitriptyline metabolite, (±)-E-10-hydroxylated- | 64520-05-4 | sc-257086 | 2 mg | $229.00 | ||
(±)-E-10-hydroxylated amitriptyline metabolite serves as a valuable analytical standard, characterized by its unique structural features that influence molecular interactions. Its hydroxyl group enhances hydrogen bonding capabilities, allowing for intricate studies of solubility and partitioning behavior in various solvents. This compound exhibits distinct chromatographic properties, facilitating separation and identification in complex mixtures, while its spectral characteristics provide critical data for understanding metabolic pathways and transformations. | ||||||
Haloxyfop-methyl | 69806-40-2 | sc-235276 | 50 mg | $57.00 | ||
Haloxyfop-methyl, an analytical standard, is notable for its specific interactions with plant enzymes, particularly in the inhibition of fatty acid synthesis. Its unique ester functionality allows for selective binding, influencing its reactivity in various analytical techniques. The compound's stability under different pH conditions enhances its utility in chromatography, while its distinct spectral profile aids in the elucidation of degradation pathways and environmental behavior, making it a key reference in analytical chemistry. | ||||||
Fenchlorazol-ethyl | 103112-35-2 | sc-257524 | 100 mg | $164.00 | ||
Fenchlorazol-ethyl is an analytical standard notable for its distinctive reactivity and molecular interactions. As an acid halide, it exhibits strong electrophilic behavior, enabling it to participate in nucleophilic acyl substitution reactions. Its unique steric configuration influences reaction kinetics, making it a valuable reference for studying reaction mechanisms. Furthermore, its solubility in various organic solvents enhances its applicability in chromatographic techniques, ensuring consistent results in analytical assessments. | ||||||
Ginkgolic acid C17:1 | 111047-30-4 | sc-228252 sc-228252A sc-228252B | 5 mg 10 mg 20 mg | $279.00 $452.00 $834.00 | 2 | |
Ginkgolic acid C17:1 serves as a critical analytical standard, characterized by its unique structural features that facilitate specific molecular interactions. As an acid, it demonstrates notable reactivity with nucleophiles, allowing for the exploration of acylation processes. Its distinct hydrophobic properties influence solubility profiles, making it suitable for various analytical techniques. Additionally, its ability to form stable complexes with metal ions provides insights into coordination chemistry, enhancing its utility in analytical applications. | ||||||
Quinoxyfen | 124495-18-7 | sc-229030 | 200 mg | $157.00 | ||
Quinoxyfen is an analytical standard distinguished by its unique molecular structure, which enables selective interactions with various biological targets. Its specific binding affinity allows for the investigation of receptor-ligand dynamics, while its stability under diverse conditions aids in reproducibility during analytical assessments. The compound's distinct electronic properties contribute to its reactivity, facilitating studies on reaction mechanisms and kinetics in complex matrices. | ||||||