Iotalamic acid or iotalamate or sodium iotalamate

Synonyms: Boc-ß-iodo-L-Ala-OMe Purity Limit: &ge 98% (HPLC) CAS No.: 93267-04-0 Molecular Formula: C9H16INO4 Molecular Weight: 329.

Application Cesium iodide (CsI) can be used as a cathode for the fabrication of field emission cathodes for potential usage in high power microwave systems. It can also be used to form an interface layer between the blocking layer and the

Application Cesium iodide (CsI) can be used as a cathode for the fabrication of field emission cathodes for potential usage in high power microwave systems. It can also be used to form an interface layer between the blocking layer and the

Application Cesium iodide can be used as precursor to synthesize lead-free perovskite material, Cs 2 NaBiI 6 (CNBI). The CNBI is highly stable and finds application in the field of solar cells, LEDs, and lasers.

Application Cesium iodide can be used as precursor to synthesize lead-free perovskite material, Cs 2 NaBiI 6 (CNBI). The CNBI is highly stable and finds application in the field of solar cells, LEDs, and lasers.

Cesium iodide is a simple ionic salt. It has the capacity to undergo second order transformation from cubic B2 structure to body-centered tetragonal structure at low pressures.

Features and Benefits Frequently used in devices such as phosphor screens for medical imaging, scintillators, calorimeters and a variety of particle detectors. Legal Information AnhydroBeads is a trademark of Sigma-Aldrich Co.

Structure confirmed. Purity = 98%. Will ship with Certificate of Analysis (CoA)

Structure confirmed. Purity = 98%. Will ship with Certificate of Analysis (CoA)

Fmoc-8-Aoc-OH

Useful derivative for introducing a side chain aldehyde functionality. The aldehyde group once protected is highly reactive and will self-condense to amine, hydroxyl and thiol functionalities in the peptide, making various cyclic and polymeric

Useful derivative for introducing a side chain aldehyde functionality. The aldehyde group once protected is highly reactive and will self-condense to amine, hydroxyl and thiol functionalities in the peptide, making various cyclic and polymeric