| Category | Click Reagents |
| Molecular Formula | C39H82N7O20P3 |
| Molecular Weight | 1062.02 |
| Appearance | White Solid |
| Storage | Store at -20°C |
Click PI(4,5)P2-azido Ammonium salt
Click PI(4,5)P2-azido Ammonium salt is a chemically modified phosphatidylinositol 4,5-bisphosphate analog that introduces an azido functional group for bioorthogonal “click” chemistry applications while maintaining the native phosphate headgroup arrangement essential for biological relevance. The azido moiety enables site-specific conjugation to fluorescent dyes, polymers, or affinity tags, facilitating visualization and crosslinking of phosphoinositide-binding proteins. The ammonium salt enhances solubility and compatibility with aqueous lipid systems. Click PI(4,5)P2-azido Ammonium salt serves as a powerful research tool for probing lipid–protein interactions, membrane signaling cascades, and the nanoscale spatial organization of phosphoinositides through controlled covalent labeling and high-precision bioconjugation strategies.
Structure of 2260669-67-6
Ordering Information
*For research and manufacturing use only. We do not sell to patients.
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cGMP Capacity
- cGMP-grade lipid manufacturing
- Scalable from milligrams to kilograms
- 20+ years expertise in lipid chemistry
- In-stock supply in the US and Europe
- Comprehensive QC testing with COA, MSD
- High-purity synthetic and natural lipids
- Covers phospholipids, sterols, and sphingolipids
- 100+ types of custom lipid modifications
- Specialized lipids for LNP delivery
- Functionalized and fluorescently labeled lipids
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- Specification
| Synonyms | 1-oleoyl-2-(6-(6-azidohexanoyl)aminohexanoyl)-sn-glycero-3-phosphoinositol-4,5-bisphosphate (ammonium salt) |
| Purity | >99% |
| Solubility | Soluble in Chloroform, Methanol, Water, Ammonium Hydroxide |
| ShelfLife | 3 Months |
| Hygroscopic | No |
| LightSensitive | No |
| PercentComposition | C 56.38%, H 9.06%, N 2.80%, O 25.57%, P 6.19% |
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