| 75818 |
Synonym: s—1-phenylethylamine, s-1-phenylethanamine, 1s-1-phenylethanamine, s—alpha-methylbenzylamine, s-1-phenylethylamine, l–alpha-methylbenzylamine, l-alpha-methylbenzylamine, s-alpha-methylbenzenemethanamine, –alpha-phenethylamine, l—1-phenylethylamine
| Boiling Point | 84°C |
| Color | Yellow |
| UN Number | 2922 |
| Formula Weight | 121.18 |
| Physical Form | Clear Liquid at 20°C |
| Chemical Name or Material | (S)-(-)-1-Phenylethylamine |
| Appearance | N/A |
| Content of Zinc | N/A |
| Boiling Point | N / A |
| Melting Point | N/A |
| Vapor Pressure | N/A |
| % Volatile by Weight | N/A |
| Solubility in Water | N/A |
| Density | N/A |
| pH of Liquid, Typical (10% soln) | N/A |
| Specific Gravity Approx | N/A |
| Odor | N/A |
| pH | N/A |
| Flash Point | N/A |
| Ignition temperature | N/A |
| Lower exposure limit | N/A |
| Upper exposure limit | N/A |
Classification of the substance or mixture
GHS Label elements, including precautionary statements
Hazards not otherwise classified (HNOC) or not covered by GHS
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S-1-Phenylethylamine is appreciated for its chiral amine structure, making it a key precursor in producing enantiomerically pure chemicals. Its phenylethylamine chemical structure makes it useful in asymmetric synthesis applications.
The phenylethylamine chemical structure leads to S-1-Phenylethylamine's distinct reactivity. Its amine group and phenyl ring allow various pharmaceutical, agrochemical, and materials science research uses.
When purchasing phenethylamine, check that it satisfies quality standards and regulatory criteria. S-1-Phenylethylamine should have a proven phenylethylamine chemical structure and be well purified to facilitate advanced research and manufacturing.
S-1-Phenylethylamine's phenylethylamine chemical structure makes it suitable for bespoke chemical formulations. Researchers frequently purchase phenethylamine for custom synthesis projects requiring high enantiomeric purity.
S-1-phenylethylamine has a unique stereochemical structure that provides enhanced selectivity in chemical processes. This distinguishing feature of its phenylethylamine chemical structure promotes its popularity in research and development.
