Ordering
Available Variants1 g
CHA.49427-1g
Price
€34.20
Available – Dispatch in 14 days
5 g
CHA.49427-5g
Price
€71.44
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.49427-1g | €34.20 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.49427-5g | €71.44 |
97%, for peptide synthesis
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
| Empirical Formula (Hill Notation) | C12H22F6N6OP2 |
|---|---|
| CAS Number | 56602-33-6 |
| Molecular Weight | 442.28 |
| NACRES | NA.22 |
| PubChem Substance ID | 24853542 |
| UNSPSC Code | 12352107 |
| EC Number | 260-279-1 |
| MDL number | MFCD00011948 |
| Beilstein/REAXYS Number | 4287025 |
Safety Information Handling visibility
| pictograms |
GHS02
GHS07
  GHS02,GHS07
|
|---|---|
| signalword | Danger |
| hcodes | H228,H315,H335 |
| pcodes | P210 - P240 - P241 - P261 - P264 - P302 + P352 |
| Hazard Classifications | Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| supp_hazards | EUH044 |
| Storage Class | 4.1A - Other explosive hazardous materials |
| 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
(Benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate, with the CAS registry number 56602-33-6, is a chemical compound that has been utilized in various applications, particularly in organic synthesis. This reagent is known for its ability to facilitate peptide coupling reactions, making it a valuable tool in the field of peptide chemistry. The compounds structure consists of a benzotriazol-1-yloxy moiety attached to a phosphonium center, which is further coordinated to three dimethylamino groups, and a hexafluorophosphate counterion. Its reactivity and stability under different conditions have been extensively studied, and it has been found to be an efficient and reliable reagent for promoting coupling reactions, especially in the synthesis of complex peptides and other organic molecules. Its properties and uses have been documented in various scientific publications, highlighting its significance in modern organic synthesis.
