Items 151 to 160 of 223 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Imidacloprid-d4 | 1015855-75-0 | sc-300824 | 10 mg | $367.00 | 1 | |
Imidacloprid-d4 is a specialized analytical standard notable for its isotopic labeling, which aids in precise quantification and tracking in analytical applications. Its unique molecular structure allows for specific interactions with biological receptors, enhancing the understanding of its behavior in environmental studies. The compound exhibits distinct reaction kinetics, making it valuable for investigating degradation pathways and metabolic processes in various matrices, ensuring reliable results in analytical assessments. | ||||||
Isoprene | 78-79-5 | sc-250194 sc-250194A | 100 ml 500 ml | $45.00 $65.00 | ||
Isoprene serves as a critical analytical standard, characterized by its unique reactivity and ability to participate in various polymerization processes. Its unsaturated structure facilitates specific interactions with electrophiles, influencing reaction pathways and kinetics. This compound's volatility and low molecular weight enhance its detection sensitivity in gas chromatography, making it essential for studying atmospheric chemistry and biogenic emissions. Its behavior in complex mixtures provides insights into environmental dynamics and organic synthesis. | ||||||
Thiosemicarbazide | 79-19-6 | sc-251239 | 100 g | $109.00 | ||
Thiosemicarbazide is a versatile analytical standard known for its ability to form stable complexes with metal ions, which can significantly influence spectroscopic measurements. Its unique thiol and amine functional groups enable specific hydrogen bonding interactions, enhancing its reactivity in various chemical environments. This compound exhibits notable stability under diverse conditions, making it suitable for studying reaction mechanisms and kinetics in coordination chemistry. Its distinct solubility properties further aid in analytical applications, allowing for effective separation and identification in complex matrices. | ||||||
2-(4-tert-Butylbenzyl)propionaldehyde | 80-54-6 | sc-254058 | 10 mg | $47.00 | ||
2-(4-tert-Butylbenzyl)propionaldehyde serves as a valuable analytical standard, characterized by its unique steric hindrance due to the bulky tert-butyl group. This feature influences its reactivity and selectivity in various chemical reactions, particularly in aldehyde condensation processes. The compound's ability to engage in specific dipole-dipole interactions enhances its role in chromatographic techniques, facilitating precise separation and identification in complex samples. Its distinctive odor profile also aids in sensory analysis applications. | ||||||
Benzyl butyl phthalate | 85-68-7 | sc-239317 sc-239317A sc-239317B | 5 ml 250 ml 1 L | $61.00 $77.00 $204.00 | ||
Benzyl butyl phthalate is an analytical standard notable for its hydrophobic characteristics and ability to form strong π-π stacking interactions due to its aromatic structure. This property enhances its stability in various solvent systems, making it ideal for chromatographic applications. Additionally, its molecular flexibility allows for diverse conformations, influencing its reactivity in esterification and transesterification reactions. These attributes contribute to its effectiveness in analytical chemistry for precise quantification and identification. | ||||||
(+)-Pulegone | 89-82-7 | sc-250804 | 5 ml | $65.00 | ||
(+)-Pulegone serves as an analytical standard distinguished by its unique chiral properties and ability to engage in hydrogen bonding, which can influence solubility and interaction with various solvents. Its cyclic structure facilitates specific conformational dynamics, impacting reaction kinetics in various chemical processes. The compound's volatility and distinct odor profile also aid in its identification and quantification in complex mixtures, making it a valuable tool in analytical methodologies. | ||||||
3-Methylpentane | 96-14-0 | sc-256538 | 1 g | $28.00 | ||
3-Methylpentane is an analytical standard characterized by its branched hydrocarbon structure, which influences its physical properties and reactivity. This compound exhibits unique molecular interactions, particularly in non-polar environments, enhancing its utility in gas chromatography. Its distinct hydrophobic characteristics facilitate separation processes, while its relatively low viscosity aids in accurate measurement and analysis. The compound's stability under various conditions further supports its role in analytical applications. | ||||||
Nitarsone | 98-72-6 | sc-228836 sc-228836A sc-228836B | 100 mg 1 g 5 g | $92.00 $184.00 $367.00 | ||
Nitarsone serves as an analytical standard notable for its unique interactions with metal ions, which can influence its behavior in complex matrices. Its distinct electronic structure allows for specific binding affinities, making it useful in studies of environmental contaminants. The compound's solubility in polar solvents enhances its detection in various analytical techniques, while its stability under oxidative conditions ensures reliable results in quantitative analyses. | ||||||
Tributylamine | 102-82-9 | sc-237261 | 100 ml | $50.00 | ||
Tributylamine is an analytical standard characterized by its unique ability to form stable complexes with various anions, facilitating studies in ion exchange processes. Its hydrophobic nature enhances partitioning in organic solvents, making it ideal for liquid-liquid extraction methods. The compound exhibits distinct nucleophilic properties, allowing it to participate in diverse reaction pathways, which can be leveraged in kinetic studies and mechanistic investigations. Its volatility aids in gas chromatography applications, ensuring precise analytical results. | ||||||
2,5-Hexanedione | 110-13-4 | sc-238390 | 100 g | $120.00 | ||
2,5-Hexanedione serves as an analytical standard notable for its reactivity in condensation reactions, particularly with amines and alcohols, leading to the formation of stable adducts. Its ability to undergo keto-enol tautomerism enhances its role in various analytical techniques, providing insights into reaction mechanisms. The compound's polar nature allows for effective solubility in both polar and nonpolar solvents, facilitating diverse extraction and separation methods in analytical chemistry. | ||||||