CHA.34928
2,2,2-Trifluoroethoxyamine hydrochloride
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Ordering
Available Variants250 mg
CHA.34928-250mg
Price
€55.38
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
250 mg | CHA.34928-250mg | €55.38 |
Professionally catalogued chemical listing prepared to support identification, technical review, safety visibility, and structured B2B sourcing workflows.
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) | C2H5ClF3NO |
|---|---|
| CAS Number | 68401-66-1 |
| Molecular Weight | 151.52 |
| NACRES | NA.22 |
| PubChem Substance ID | 329767243 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD13196692 |
| Form | solid |
Safety Information Handling visibility
| pictograms |
GHS07
GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H302 |
| pcodes | P301 + P312 + P330 |
| Hazard Classifications | Acute Tox. 4 Oral |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
2,2,2-Trifluoroethoxyamine hydrochloride, with the CAS number 68401-66-1, is a chemical compound that has been utilized in various applications, primarily in the realm of pharmaceuticals and organic synthesis. This compound exhibits unique properties due to the presence of the trifluoroethoxy group, which imparts distinct reactivity and stability characteristics. As a hydrochloride salt, it is highly soluble in water and other polar solvents, making it a convenient intermediate for further chemical transformations. The trifluoroethoxyamine moiety can participate in a range of reactions, including nucleophilic substitutions and additions, allowing for the synthesis of complex molecules with potential biological activity. Its applications continue to be explored in fields such as medicinal chemistry, where the incorporation of fluorine-containing groups can significantly impact the pharmacokinetic and pharmacodynamic properties of drug candidates.
