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Available Variants5 g
CHA.23767-5g
Price
€95.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.23767-5g | €95.40 |
98%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Linear Formula | C6H5CH2O(CH2)3P(C6H5)3Br |
|---|---|
| CAS Number | 54314-85-1 |
| Molecular Weight | 491.40 |
| NACRES | NA.22 |
| PubChem Substance ID | 24864267 |
| UNSPSC Code | 12352112 |
| MDL number | MFCD00191781 |
| Assay | 98% |
| Form | powder |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H315,H319,H335 |
| pcodes | P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
(3-Benzyloxypropyl)triphenylphosphonium bromide, with a CAS number of 54314-85-1, is a phosphonium salt that has been utilized in various chemical reactions. This compound is typically prepared through the reaction of triphenylphosphine with a suitable alkyl halide, such as 3-benzyloxypropyl bromide. The resulting phosphonium salt can then be employed as a reagent in a range of applications, including the synthesis of complex organic molecules and the formation of ylides, which are useful intermediates in organic synthesis. The properties of (3-benzyloxypropyl)triphenylphosphonium bromide make it a valuable tool for chemists, allowing for the introduction of specific functional groups into target molecules and facilitating the development of new synthetic methodologies. Its reactivity and versatility have led to its incorporation into various research protocols and synthetic strategies.
