BIS(DIMETHYLAMINO)PHOSPHORYL CHLORIDE
97%
- Product Code: 72985
Alias:
Bis(N,N-Dimethylamino)phosphonyl Chloride; Bis(Dimethylamino)phosphoryl Chloride; N,N,N,N-Tetramethyldiaminophosphoryl Chloride
CAS:
1605-65-8
| Molecular Weight: | 170.58 g./mol | Molecular Formula: | C₄H₁₂ClN₂OP |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00008302 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, sealed |
Product Description:
Used primarily in organic synthesis as a phosphorylating agent, it facilitates the introduction of the dimethylamino phosphate group into various molecules. This compound is particularly valuable in the production of pharmaceuticals, where it aids in the creation of active drug ingredients. It also plays a role in the synthesis of agrochemicals, contributing to the development of pesticides and herbicides. Additionally, it is utilized in the preparation of flame retardants, enhancing the safety of materials by reducing their flammability. Its reactivity with nucleophiles makes it a versatile reagent in the modification of polymers and other complex organic structures.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97-100 |
| REFRACTURE INDEX N20D | 1.463-1.469 |
| APPEARANCE | COLORLESS TO PALE YELLOW LIQUID |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿300.00 |
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| 5.000 | 10-20 days | ฿600.00 |
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| 25.000 | 10-20 days | ฿2,560.00 |
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BIS(DIMETHYLAMINO)PHOSPHORYL CHLORIDE
Used primarily in organic synthesis as a phosphorylating agent, it facilitates the introduction of the dimethylamino phosphate group into various molecules. This compound is particularly valuable in the production of pharmaceuticals, where it aids in the creation of active drug ingredients. It also plays a role in the synthesis of agrochemicals, contributing to the development of pesticides and herbicides. Additionally, it is utilized in the preparation of flame retardants, enhancing the safety of materials by reducing their flammability. Its reactivity with nucleophiles makes it a versatile reagent in the modification of polymers and other complex organic structures.
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