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Atomfair Tri-2-propyn-1-yl phosphate C9H9O4P
Description Tri-2-propyn-1-yl phosphate (CAS No. 1779-34-6) is a high-purity organophosphorus compound with the molecular formula C9H9O4P and the IUPAC name tris(prop-2-ynyl) phosphate . This specialty chemical is characterized by its triple-bonded propargyl groups, which impart unique reactivity for advanced synthetic applications. Our product is synthesized under strict quality control to ensure optimal purity and consistency for research and industrial use. It is supplied as a clear to pale yellow liquid with careful packaging to maintain stability. Ideal for flame retardant research, polymer modification, and click chemistry applications due to its terminal alkyne functionality. Technical data including NMR, HPLC, and MS…
Description
Description
Tri-2-propyn-1-yl phosphate (CAS No. 1779-34-6) is a high-purity organophosphorus compound with the molecular formula C9H9O4P and the IUPAC name tris(prop-2-ynyl) phosphate. This specialty chemical is characterized by its triple-bonded propargyl groups, which impart unique reactivity for advanced synthetic applications. Our product is synthesized under strict quality control to ensure optimal purity and consistency for research and industrial use. It is supplied as a clear to pale yellow liquid with careful packaging to maintain stability. Ideal for flame retardant research, polymer modification, and click chemistry applications due to its terminal alkyne functionality. Technical data including NMR, HPLC, and MS spectra are available upon request to support your analytical needs.
- CAS No: 1779-34-6
- Molecular Formula: C9H9O4P
- Molecular Weight: 212.14
- Exact Mass: 212.02384576
- Monoisotopic Mass: 212.02384576
- IUPAC Name: tris(prop-2-ynyl) phosphate
- SMILES: C#CCOP(=O)(OCC#C)OCC#C
- Synonyms: 1779-34-6, Tri-2-propyn-1-yl phosphate, 853-966-8, tripropargyl phosphate, tris(prop-2-ynyl) phosphate
Application
Tri-2-propyn-1-yl phosphate serves as a versatile intermediate in flame retardant formulations due to its phosphorus content and propargyl groups. Researchers utilize this compound in polymer chemistry for crosslinking reactions and as a building block for advanced materials. Its terminal alkynes make it valuable for Huisgen cycloaddition (click chemistry) in bioconjugation and pharmaceutical development.
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