N-Methyl-1-phenylpropylamine

≥98%(GC)

Reagent Code: #217602
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CAS Number 7713-71-5

science Other reagents with same CAS 7713-71-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 149.24 g/mol
Formula C₁₀H₁₅N
badge Registry Numbers
MDL Number MFCD04038424
thermostat Physical Properties
Boiling Point 96°C|20mmHg(lit.)
inventory_2 Storage & Handling
Density 0.92
Storage Room temperature, dryness, inert gas storage

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and fine chemicals. Its structure supports the development of chiral agents useful in asymmetric synthesis. It may also find use in the manufacture of specialty amines for agrochemicals or pharmaceuticals, where the N-methyl and phenyl groups contribute to bioactivity or serve as a building block for more complex molecules. Due to its amine functionality, it can participate in alkylation, acylation, and reductive amination reactions, making it valuable in research and industrial settings for creating nitrogen-containing compounds.

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inventory 1ml
10-20 days ฿3,880.00

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N-Methyl-1-phenylpropylamine
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and fine chemicals. Its structure supports the development of chiral agents useful in asymmetric synthesis. It may also find use in the manufacture of specialty amines for agrochemicals or pharmaceuticals, where the N-methyl and phenyl groups contribute to bioactivity or serve as a building block for more complex molecules. Due to its amine functionality, it can participate in alkylation, ac

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and fine chemicals. Its structure supports the development of chiral agents useful in asymmetric synthesis. It may also find use in the manufacture of specialty amines for agrochemicals or pharmaceuticals, where the N-methyl and phenyl groups contribute to bioactivity or serve as a building block for more complex molecules. Due to its amine functionality, it can participate in alkylation, acylation, and reductive amination reactions, making it valuable in research and industrial settings for creating nitrogen-containing compounds.

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