Items 41 to 46 of 46 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Prostaglandin B2-d4 | sc-224214A sc-224214 | 50 µg 100 µg | $67.00 $95.00 | |||
Prostaglandin B2-d4 serves as a valuable mass spectrometry standard, distinguished by its deuterated structure that enhances analytical precision. This compound demonstrates unique fragmentation pathways, leading to specific ion signatures that improve detection sensitivity. Its isotopic labeling allows for accurate quantification in complex biological samples, while its interactions during ionization contribute to reproducible results in lipid analysis and metabolic studies, making it an essential tool for researchers. | ||||||
tetranor-PGEM-d6 | 1240398-16-6 | sc-224306 sc-224306A | 25 µg 50 µg | $440.00 $835.00 | ||
Tetranor-PGEM-d6 serves as a precise mass spectrometry standard, notable for its deuterated structure that enhances analytical sensitivity. This compound demonstrates unique fragmentation pathways, producing distinct ion signatures that facilitate accurate identification and quantification. Its stable isotopic labeling allows for reproducible results, making it an essential tool for distinguishing between closely related metabolites in complex biological matrices. The compound's specific interactions with ionization sources further optimize its performance in mass spectrometric analyses. | ||||||
ent-8-iso Prostaglandin F2α-d9 | sc-221588 sc-221588A | 10 µg 25 µg | $185.00 $592.00 | |||
Ent-8-iso Prostaglandin F2α-d9 is a specialized mass spectrometry standard characterized by its deuterated configuration, which facilitates enhanced resolution in analytical applications. This compound exhibits distinct ionization behavior, resulting in unique mass spectral patterns that aid in differentiating it from non-labeled analogs. Its specific fragmentation routes contribute to reliable quantification, while its stable isotopic nature ensures consistent performance across various experimental conditions, making it a critical reference for lipidomic studies. | ||||||
Bimatoprost-d4 | sc-221361 sc-221361A | 25 µg 50 µg | $101.00 $190.00 | |||
Bimatoprost-d4 serves as a precise mass spectrometry standard, distinguished by its deuterated isotopes that enhance analytical sensitivity. Its unique molecular structure influences ionization efficiency, resulting in specific and reproducible fragmentation pathways. This compound exhibits remarkable stability during ionization, facilitating accurate mass determination. The isotopic labeling allows for effective differentiation in complex mixtures, ensuring reliable quantification and calibration in diverse analytical applications. | ||||||
Abnormal Cannabidiol-d3 | sc-223766 sc-223766A sc-223766B sc-223766C | 100 µg 500 µg 1 mg 5 mg | $62.00 $280.00 $497.00 $2182.00 | |||
Abnormal Cannabidiol-d3 is a specialized mass spectrometry standard characterized by its unique isotopic labeling, which aids in enhancing detection limits. This compound exhibits distinct ionization behavior, leading to specific fragmentation patterns that yield recognizable mass spectra. Its unique structural features contribute to reliable calibration curves, ensuring consistent quantification across various analytical conditions. The compound's stability under ionization conditions further supports its role in complex sample analysis, making it a valuable reference standard. | ||||||
trans-4-Hydroxy-3-methoxycinnamic acid | 537-98-4 | sc-272656 sc-272656A sc-272656B sc-272656C | 25 g 250 g 500 g 1 kg | $109.00 $143.00 $245.00 $398.00 | ||
Trans-4-Hydroxy-3-methoxycinnamic acid is a versatile compound recognized for its unique structural features that influence its behavior in mass spectrometry. Its hydroxyl and methoxy groups enhance polarity, facilitating ionization and improving detection sensitivity. The compound exhibits distinct fragmentation patterns, allowing for precise identification in complex mixtures. Additionally, its conjugated double bond system contributes to unique electronic properties, influencing its reactivity and interaction with other analytes. |