Triethylenephosphoramide

CAS: 545-55-1

Ref. 3D-FT28432

Produktinformation

• Name: Triethylenephosphoramide
• Synonyme: 1,1',1''-PhosphinylidynetrisaziridineTris(1-aziridinyl)phosphine oxideAPO, 1,1',1''-Phosphinylidynetrisaziridine, 1,1',1''-Phosphoryltriaziridine, 1,1′,1′′-Phosphinylidynetris[aziridine], A 6366, APO, Ai3-24915, Aphoxide, Aziridine, 1,1',1"-phosphinylidynetris-, Aziridine, 1,1′,1′′-phosphinylidynetris-, Brn 0145971, Cbc 906288, Ent 24915, Hexamethylphosphoric triamide tris(1-aziridinyl)phosphine oxide, Hsdb 1011, Imperon fixer T, N,N',N -triethylenephosphoramide, N,N',N''-Tri-1,2-ethanediylphosphoric triamide, N,N',N''-Triethylenephosphoric triamide, Nsc 9717, Phosphine oxide, tris(1-aziridinyl)-, Phosphoramide, N,N',N -triethylene-, Phosphoric acid triethylene imide, Phosphoric triamide, N,N',N -triethylene-, Phosphoric triamide, N,N',N''-tri-1,2-ethanediyl-, Sk-3818, TEF, TEPA (pesticide), Tapo, Tepa, Tri-1-aziridinylphosphine oxide, Triaethylenphosphorsaeureamid, Triaethylenphosphorsaeureamid [German], Triaziridinophosphine oxide, Triaziridinylphosphine oxide, Triethylene phophoramide, Triethylene phosphoramide, Triethylenephosphoric triamide, Triethylenephosphorotriamide, Triethylenepyrophosphoramide, Triethylenfosforamid, Triethylenfosforamid [Czech], Tris(1-aziridine)phosphine oxide, Tris(1-aziridinyl)phosphine oxide, Tris(1-aziridinyl)phosphine oxide, solution, Tris(1-aziridinyl)phosphine oxide, solution [UN2501] [Poison], Tris(N-ethylene)phosphorotriamidate, Tris(aziridinyl)phosphine oxide, Tris-(1-aziridinyl)-phosphineoxide, Tris-(1-aziridinyl)fosfinoxid, Tris-(1-aziridinyl)fosfinoxid [Czech], Un2501, Tri(aziridin-1-yl)phosphine oxide, 4-20-00-00048 (Beilstein Handbook Reference)

Beschreibung

Triethylenephosphoramide (TEP) is a model system for studying the reaction mechanism of the enzyme phosphotriesterase. TEP has been used in reactions with water vapor, which causes the release of hydrogen chloride. The reaction solution is analyzed by mass spectrometry to determine the reaction products. TEP has also been shown to inhibit nitrite ion-dependent enzymes such as nitrate reductase and aminopeptidase N. TEP reacts with fluorescence probes that have been modified with response elements to detect the binding of these probes to DNA and RNA. This helps researchers identify the location of TEP in proteins and nucleic acids.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 173.15 g/mol
• Formel: C₆H₁₂N₃OP
• Reinheit: Min. 95%
• Farbe/Form: Powder
• InChl: InChI=1S/C6H12N3OP/c10-11(7-1-2-7,8-3-4-8)9-5-6-9/h1-6H2
• InChI Key: InChIKey=FYAMXEPQQLNQDM-UHFFFAOYSA-N
• SMILES: O=P(N1CC1)(N1CC1)N1CC1