| 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 |
| Formula Weight | 121.18 |
| Physical Form | Clear Liquid at 20°C |
| Chemical Name or Material | (S)-(-)-1-Phenylethylamine |
| UN Number | 2922 |
Classification of the substance or mixture
GHS Label elements, including precautionary statements
Hazards not otherwise classified (HNOC) or not covered by GHS
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS). For the full text of the H-Statements mentioned in this Section, see Section 16.
Signal word :
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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.
