Items 81 to 90 of 222 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Fluoranthene-d10 | 93951-69-0 | sc-257534 | 50 mg | $138.00 | ||
Fluoranthene-d10 serves as a valuable analytical standard, characterized by its unique isotopic labeling that enhances detection sensitivity in mass spectrometry. Its distinct molecular structure allows for specific interactions with various chromatographic media, improving separation efficiency. The compound exhibits notable fluorescence properties, enabling effective monitoring in environmental and chemical analyses. Additionally, its stability under varying conditions ensures consistent results across diverse analytical methodologies. | ||||||
1,3,5-Trimethylbenzene | 108-67-8 | sc-255931 | 100 ml | $46.00 | ||
1,3,5-Trimethylbenzene serves as a vital analytical standard, characterized by its symmetrical structure that promotes consistent behavior in various analytical methods. Its unique electron-rich aromatic system enhances interactions with electrophiles, facilitating reaction kinetics in electrophilic aromatic substitution. The compound's hydrophobic nature allows for effective separation in non-polar environments, while its distinct vapor pressure properties contribute to its utility in gas chromatography. | ||||||
Penicillin V Potassium | 132-98-9 | sc-204839 sc-204839A | 10 g 25 g | $48.00 $78.00 | ||
Penicillin V Potassium, as an analytical standard, exhibits unique solubility characteristics that enhance its stability in aqueous solutions, making it ideal for various analytical techniques. Its ability to form hydrogen bonds influences its interaction with polar solvents, affecting retention times in chromatography. Additionally, the compound's specific stereochemistry plays a crucial role in its reactivity, allowing for precise quantification in complex mixtures through spectroscopic methods. | ||||||
Methapyrilene HCl | 135-23-9 | sc-257708 | 1 g | $98.00 | ||
Methapyrilene HCl serves as a valuable analytical standard due to its distinctive interaction with various solvents, which facilitates its solubility and stability in diverse analytical environments. Its unique electronic structure allows for specific charge distribution, influencing reaction kinetics and enhancing detection sensitivity in spectrometric analyses. Furthermore, the compound's capacity to engage in dipole-dipole interactions aids in its separation efficiency during chromatographic processes, ensuring accurate quantification in complex samples. | ||||||
2,4,5-Trimethylaniline | 137-17-7 | sc-254345 | 2 g | $400.00 | ||
2,4,5-Trimethylaniline is an important analytical standard characterized by its unique steric hindrance and electron-donating properties, which influence its reactivity in electrophilic aromatic substitution reactions. Its ability to form stable complexes with metal ions enhances its role in coordination chemistry. Additionally, the compound exhibits strong π-π stacking interactions, improving its retention in chromatographic techniques and contributing to precise analytical measurements in complex matrices. | ||||||
Piperazine hexahydrate | 142-63-2 | sc-250728 | 200 g | $49.00 | ||
Piperazine hexahydrate serves as a crucial analytical standard, notable for its ability to form hydrogen bonds and engage in dipole-dipole interactions, which enhance solubility in various solvents. Its unique cyclic structure allows for specific conformational flexibility, influencing reaction kinetics in nucleophilic substitution processes. Additionally, its hygroscopic nature aids in maintaining consistent moisture levels in analytical environments, ensuring reliable results in quantitative analyses. | ||||||
Quercitrin | 522-12-3 | sc-280045 sc-280045A | 50 mg 100 mg | $242.00 $278.00 | 2 | |
Quercitrin is an important analytical standard characterized by its ability to form strong hydrogen bonds and engage in π-π stacking interactions, which enhance its stability in solution. Its glycosidic structure contributes to distinct solubility profiles across different solvents, facilitating diverse analytical applications. The compound's reactivity in oxidation and reduction pathways is notable, allowing for precise monitoring of reaction kinetics in various experimental setups. | ||||||
Delphinidin chloride | 528-53-0 | sc-202572 | 10 mg | $401.00 | 2 | |
Delphinidin chloride serves as a vital analytical standard, distinguished by its unique chromophoric properties that enable effective UV-Vis spectrophotometric analysis. Its ability to form stable complexes with metal ions enhances its role in chelation studies. Additionally, the compound exhibits notable fluorescence characteristics, making it suitable for sensitive detection methods. Its structural features allow for specific interactions with biomolecules, providing insights into molecular dynamics and behavior in various environments. | ||||||
Altrenogest | 850-52-2 | sc-233848 sc-233848A sc-233848B sc-233848C sc-233848D | 100 mg 250 mg 1 g 5 g 10 g | $102.00 $242.00 $604.00 $2448.00 $4641.00 | ||
Altrenogest, as an analytical standard, is characterized by its distinct stereochemistry, which influences its binding affinity to various receptors. This compound exhibits unique solubility profiles in different solvents, facilitating its use in chromatography. Its stability under varying pH conditions allows for reliable quantification in diverse analytical methods. Furthermore, Altrenogest's capacity for specific molecular interactions aids in elucidating reaction mechanisms and kinetics in biochemical assays. | ||||||
Potassium phthalate monobasic | 877-24-7 | sc-203363 sc-203363A sc-203363B sc-203363C sc-203363D | 100 g 500 g 1 kg 2.5 kg 5 kg | $41.00 $99.00 $179.00 $316.00 $571.00 | ||
Potassium phthalate monobasic serves as a crucial analytical standard, notable for its ability to form stable complexes with metal ions, enhancing its role in titrimetric analyses. Its unique buffering capacity allows for precise pH control in various experimental setups. The compound's distinct solubility characteristics enable effective separation techniques, while its reactivity with specific functional groups aids in the study of reaction pathways and kinetics in analytical chemistry. | ||||||