![(+)-Bis[(R)-1-phenylethyl]amine molecular structure](/images/molecules/--bis-r--1-phenylethyl-amine-23294-41-9.png)
Ordering
Available Variants1 g
CHA.44469-1g
Price
€49.68
Available – Dispatch in 14 days
10 g
CHA.44469-10g
Price
€323.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.44469-1g | €49.68 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
10 g | CHA.44469-10g | €323.20 |
99%
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.
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Technical Specifications Structured product data
| Linear Formula | [C6H5CH(CH3)]2NH |
|---|---|
| CAS Number | 23294-41-9 |
| Molecular Weight | 225.33 |
| UNSPSC Code | 12352116 |
| NACRES | NA.22 |
| PubChem Substance ID | 24868728 |
| MDL number | MFCD00243088 |
| Beilstein/REAXYS Number | 3590931 |
| Assay | 99% |
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 | 10 - Combustible liquids |
| wgk | WGK 3 |
| flash_point_f | >235.4 °F - closed cup |
| flash_point_c | > 113 °C - closed cup |
| ppe | Eyeshields, Gloves, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
(+)-Bis[(R)-1-phenylethyl]amine, with a CAS number of 23294-41-9, is a chiral diamine compound that has garnered significant attention in the field of organic chemistry. Its molecular structure consists of two (R)-1-phenylethyl groups attached to a central nitrogen atom, resulting in a molecule with distinct stereochemical properties. This compound has been utilized as a chiral ligand in various asymmetric catalytic reactions, including hydrogenation and cycloaddition reactions. The ability of (+)-Bis[(R)-1-phenylethyl]amine to form complexes with metal centers and influence the stereochemical outcome of reactions has made it a valuable tool in the synthesis of enantiomerically pure compounds. Its applications extend to the production of pharmaceuticals and fine chemicals, where the control of molecular stereochemistry is crucial.
