181471-62-5

Basic information

• Product Name: 1-TERT-BUTYL-4,4,4-TRIS(DIMETHYLAMINO)-2,2-BIS[TRIS(DIMETHYLAMINO) PHOSPHORANYLIDE-NAMINO]-2LAMBDA5,4LAMBDA5-CATENADI(PHOSPHAZENIUM) BF4
• Synonyms: 1-TERT-BUTYL-4,4,4-TRIS(DIMETHYLAMINO)-2,2-BIS[TRIS(DIMETHYLAMINO) PHOSPHORANYLIDE-NAMINO]-2LAMBDA5,4LAMBDA5-CATENADI(PHOSPHAZENIUM) BF4;PHOSPHAZENE BASE P4-T-BU TETRAFLUOROBORATE SALT;1-tert-butyl-4,4,4-tris(dimethylamino)-2,2-bis[tris(dimethylamino)-phosphoranylidenamino]-2Λ5,4Λ5-catenadi(phosphazenium) tetrafluoroborate salt;1-tert-Butyl-4,4,4-tris(dimethylamino)-2,2-bis[tris(dimethylamino)-phosphoranylidenamino]-2Λ:5,4Λ:5-catenadi(phosphazenium) tetrafluoroborate salt;Phosphazene base P4-t-Bu tetrafluoroborate salt purum, >=97.0% (NMR)
• CAS NO: 181471-62-5
• Molecular Formula: C22H63N13P4
• Molecular Weight: 721.53
• Mol File: 181471-62-5.mol
• Article Data: 0

Chemical Properties

• Melting Point: 330-340 °C (dec.)
• Appearance: /
• CAS DataBase Reference: 1-TERT-BUTYL-4,4,4-TRIS(DIMETHYLAMINO)-2,2-BIS[TRIS(DIMETHYLAMINO) PHOSPHORANYLIDE-NAMINO]-2LAMBDA5,4LAMBDA5-CATENADI(PHOSPHAZENIUM) BF4(CAS DataBase Reference)
• NIST Chemistry Reference: 1-TERT-BUTYL-4,4,4-TRIS(DIMETHYLAMINO)-2,2-BIS[TRIS(DIMETHYLAMINO) PHOSPHORANYLIDE-NAMINO]-2LAMBDA5,4LAMBDA5-CATENADI(PHOSPHAZENIUM) BF4(181471-62-5)
• EPA Substance Registry System: 1-TERT-BUTYL-4,4,4-TRIS(DIMETHYLAMINO)-2,2-BIS[TRIS(DIMETHYLAMINO) PHOSPHORANYLIDE-NAMINO]-2LAMBDA5,4LAMBDA5-CATENADI(PHOSPHAZENIUM) BF4(181471-62-5)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 181471-62-5(Hazardous Substances Data)

Usage

Type of compound

Phosphazene-based catalyst
A compound containing phosphazene (a ring structure containing alternating nitrogen and phosphorus atoms) that acts as a catalyst in various chemical reactions.

Structural components

Tetrakis(dimethylamino)phosphazenium cation
A positively charged ion with a phosphazene ring and four dimethylamino groups attached to it.
Tetrafluoroborate anion
A negatively charged ion consisting of four fluorine atoms attached to a boron atom.

Charge

+1 (cation) and -1 (anion)
The compound consists of a positively charged cation and a negatively charged anion, maintaining electrical neutrality.

Applications

Ring-opening polymerization
A process in which cyclic polymers are synthesized from monomers using a catalyst.
Hydroboration
A reaction involving the addition of borane (BH3) to an unsaturated compound, typically an alkene or alkyne.
Asymmetric synthesis
A reaction that produces chiral molecules with a specific three-dimensional arrangement of atoms, which is important in the production of pharmaceuticals and other fine chemicals.

Unique properties

High efficiency
The catalyst is highly effective in promoting the desired chemical reactions.
Stability
The catalyst remains unchanged and active under various reaction conditions.

Interest in the field

Organometallic chemistry
A subfield of chemistry that focuses on compounds containing metal-carbon bonds.
Organic synthesis
A branch of chemistry that involves the construction of complex organic molecules from simpler precursors.

Potential for catalyzing a wide range of chemical transformations

Due to its unique structure and electronic properties, PTA-L4 has shown great potential in catalyzing various chemical reactions, making it a valuable tool in the field of chemistry.