Ordering
Available Variants5 g
CHA.59978-5g
Price
€41.58
Available – Dispatch in 14 days
25 g
CHA.59978-25g
Price
€131.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.59978-5g | €41.58 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.59978-25g | €131.20 |
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 | BrCH2P(Br)(C6H5)3 |
|---|---|
| CAS Number | 1034-49-7 |
| Molecular Weight | 436.12 |
| NACRES | NA.22 |
| UNSPSC Code | 12352002 |
| PubChem Substance ID | 24856314 |
| EC Number | 213-857-2 |
| Beilstein/REAXYS Number | 3579901 |
| MDL number | MFCD00011864 |
| Assay | 98% |
| Form | solid |
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
(Bromomethyl)triphenylphosphonium bromide, with the CAS registry number 1034-49-7, is a quaternary phosphonium salt that has been utilized in various organic synthesis reactions. This compound is typically prepared by the reaction of triphenylphosphine with bromomethane, resulting in the formation of a phosphonium salt. The bromomethyl group in this compound serves as a versatile functional group, allowing it to participate in numerous reactions such as nucleophilic substitution and Wittig reactions. As a reagent, (bromomethyl)triphenylphosphonium bromide has been employed in the synthesis of complex molecules, including natural products and pharmaceuticals, due to its ability to introduce a bromomethyl group into target molecules. Its applications in organic synthesis have been well-documented, highlighting its importance as a valuable reagent in modern chemistry.
