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Catalog Number:
37442
CAS Number:
1608-26-0
Tris(dimetilamino)fosfina
Purity:
≥ 98% (GC)
Synonym(s):
Triamida hexametilfosforosa, Hexametiltriamidofosfito
Hazmat
Documents
$55.48 /25G
Tamaño
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Product Information

Se utiliza como reactivo en síntesis orgánica como agente fosforilante.

Synonyms
Triamida hexametilfosforosa, Hexametiltriamidofosfito
CAS Number
1608-26-0
Purity
≥ 98% (GC)
Molecular Formula
C6H18N3P
Molecular Weight
163.2
MDL Number
MFCD00008301
PubChem ID
15355
Melting Point
-44 °C
Density
0.898
Appearance
Líquido incoloro
Boiling Point
162 - 164 °C
Refractive Index
1.46
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Triamida hexametilfosforosa, Hexametiltriamidofosfito
CAS Number
1608-26-0
Purity
≥ 98% (GC)
Molecular Formula
C6H18N3P
Molecular Weight
163.2
MDL Number
MFCD00008301
PubChem ID
15355
Melting Point
-44 °C
Density
0.898
Appearance
Líquido incoloro
Boiling Point
162 - 164 °C
Refractive Index
1.46
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Tris(dimethylamino)phosphine is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in the synthesis of various organic compounds, particularly in the formation of phosphine derivatives, which are crucial in pharmaceutical development.
  • Catalysis: It acts as a catalyst in several chemical reactions, enhancing reaction rates and yields, making it valuable in the production of fine chemicals and agrochemicals.
  • Material Science: Tris(dimethylamino)phosphine is used in the development of advanced materials, including polymers and coatings, due to its ability to modify surface properties and improve durability.
  • Electronics: In the semiconductor industry, it is employed in the deposition of phosphorous-containing thin films, which are essential for the fabrication of electronic devices.
  • Biochemistry: This compound is utilized in biochemical research for its role in modifying biomolecules, aiding in the study of enzyme functions and interactions.

Citas