Chemical structure of 1,1,-Bis (4-Chlorophenyl)-2,2,2-Trichloroethane 4,4'-DTT | 50-29-3
SKU: S2382

(S)-(-)-1-Phenylethylamine | 2627-86-3 |Sarcham Labs

SKU: S2382

Description

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

SPECIFICATION

AppearanceN/A
Content of ZincN/A
Boiling PointN / A
Melting PointN/A
Vapor PressureN/A
% Volatile by WeightN/A
Solubility in WaterN/A
DensityN/A
pH of Liquid, Typical (10% soln)N/A
Specific Gravity ApproxN/A
OdorN/A
pHN/A
Flash PointN/A
Ignition temperatureN/A
Lower exposure limitN/A
Upper exposure limitN/A

Safety Information

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 | 2627-86-3 FAQs

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.