Items 51 to 60 of 222 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Methyl Pentacosanoate | 55373-89-2 | sc-205387 sc-205387A | 10 mg 50 mg | $20.00 $56.00 | 2 | |
Methyl Pentacosanoate serves as a crucial analytical standard, characterized by its long-chain fatty acid structure that influences its solubility and interaction with various solvents. This compound exhibits unique hydrophobic properties, facilitating studies on lipid interactions and membrane dynamics. Its distinct spectral features, particularly in NMR and mass spectrometry, enable precise identification and quantification, making it invaluable for analyzing complex biological samples and environmental matrices. | ||||||
Lisinopril | 76547-98-3 | sc-205378 sc-205378A | 100 mg 500 mg | $20.00 $41.00 | 2 | |
Lisinopril, as an analytical standard, is notable for its ability to form stable complexes with metal ions, enhancing its utility in coordination chemistry studies. Its polar functional groups contribute to strong hydrogen bonding interactions, influencing solubility in various solvents. The compound's distinct UV-Vis absorption characteristics allow for effective monitoring in chromatographic techniques, facilitating the analysis of reaction kinetics and the behavior of related compounds in complex mixtures. | ||||||
(±)-Sulfinpyrazone | 57-96-5 | sc-202822 sc-202822A | 1 g 5 g | $42.00 $94.00 | 2 | |
(±)-Sulfinpyrazone serves as a valuable analytical standard due to its unique ability to engage in specific molecular interactions, particularly through its sulfonamide group, which can participate in hydrogen bonding and dipole-dipole interactions. This compound exhibits distinct spectroscopic properties, making it suitable for UV-Vis and NMR analysis. Its reactivity profile allows for the investigation of oxidation-reduction pathways, providing insights into reaction kinetics and mechanisms in various analytical applications. | ||||||
Girard′s Reagent P | 1126-58-5 | sc-295008 | 25 g | $185.00 | 2 | |
Girard's Reagent P is an analytical standard notable for its ability to form stable derivatives with carbonyl compounds through nucleophilic addition. This reagent features a quaternary ammonium group, enhancing its solubility in polar solvents and facilitating selective reactions. Its distinct spectroscopic characteristics, including strong UV absorbance, enable precise quantification and identification in complex mixtures. Additionally, its reactivity with aldehydes and ketones allows for the exploration of reaction mechanisms and pathways in analytical chemistry. | ||||||
γ-Tocotrienol | 14101-61-2 | sc-205529 sc-205529A | 1 mg 10 mg | $49.00 $356.00 | 2 | |
γ-Tocotrienol serves as a valuable analytical standard due to its unique structural features, including a long hydrophobic tail that influences its solubility and interaction with lipid matrices. Its antioxidant properties allow for the study of lipid peroxidation processes, while its distinct UV-Vis absorption spectrum aids in quantification. The compound's ability to engage in specific molecular interactions with membranes makes it a useful tool for investigating lipid dynamics and cellular behavior in analytical contexts. | ||||||
Asiaticoside | 16830-15-2 | sc-257101 sc-257101A sc-257101B sc-257101C sc-257101D | 5 mg 25 mg 100 mg 1 g 10 g | $112.00 $203.00 $617.00 $1121.00 $4079.00 | 1 | |
Asiaticoside is an analytical standard characterized by its glycosidic structure, which facilitates specific interactions with various biological macromolecules. Its unique ability to form hydrogen bonds enhances solubility in polar solvents, making it suitable for chromatographic techniques. The compound exhibits distinct fluorescence properties, allowing for sensitive detection in analytical assays. Additionally, its stability under various pH conditions enables reliable quantification in diverse experimental setups. | ||||||
Ibuprofen sodium salt | 31121-93-4 | sc-252898 sc-252898A | 100 g 500 g | $201.00 $733.00 | 7 | |
Ibuprofen sodium salt serves as an analytical standard notable for its ionic nature, which influences solubility and reactivity in aqueous environments. Its ability to engage in electrostatic interactions enhances its compatibility with various analytical techniques, including spectrophotometry and chromatography. The compound's distinct dissociation behavior in solution allows for precise calibration in quantitative analyses, while its stability across a range of temperatures ensures consistent performance in experimental applications. | ||||||
Chromoionophore IV | 124522-01-6 | sc-252602 | 10 mg | $317.00 | ||
Chromoionophore IV is an analytical standard characterized by its unique ability to selectively bind cations, facilitating the study of ion transport mechanisms. Its distinct chromogenic properties enable real-time monitoring of ion concentrations through colorimetric changes. The compound exhibits rapid kinetics in ion exchange processes, making it ideal for dynamic studies. Additionally, its solubility in organic solvents enhances its versatility in various analytical methodologies, providing reliable calibration for complex matrices. | ||||||
4-Nitroquinoline N-oxide | 56-57-5 | sc-256815 sc-256815A | 1 g 5 g | $124.00 $421.00 | 6 | |
4-Nitroquinoline N-oxide serves as a valuable analytical standard due to its distinctive electron-accepting properties, which enable it to participate in redox reactions. This compound exhibits notable fluorescence characteristics, allowing for sensitive detection in various analytical techniques. Its ability to form stable complexes with metal ions enhances its utility in studying coordination chemistry. Furthermore, its solubility in polar solvents supports diverse applications in analytical chemistry, ensuring accurate quantification in complex samples. | ||||||
Heptachlor | 76-44-8 | sc-338741 | 100 mg | $408.00 | ||
Heptachlor is an analytical standard recognized for its unique hydrophobic interactions and stability in various solvents, which facilitate its detection in environmental samples. Its persistent nature allows for the study of degradation pathways and bioaccumulation in ecological assessments. Additionally, Heptachlor's ability to form strong van der Waals forces enhances its interactions with organic matrices, making it a critical compound for investigating pesticide residues and environmental monitoring. | ||||||