1-m-tolylethanamine hydrochloride

≥95%

Reagent Code: #205691
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CAS Number 856629-05-5

science Other reagents with same CAS 856629-05-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.67 g/mol
Formula C₉H₁₄ClN
badge Registry Numbers
MDL Number MFCD22570312
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of active ingredients requiring chiral amine functionalities, particularly in the development of central nervous system agents and selective receptor ligands. Commonly employed in research settings for the construction of more complex amine-containing molecules due to its stability as a hydrochloride salt. Also utilized in asymmetric synthesis and catalysis where the toluidine backbone offers steric and electronic advantages.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,690.00
inventory 250mg
10-20 days ฿4,560.00

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1-m-tolylethanamine hydrochloride
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of active ingredients requiring chiral amine functionalities, particularly in the development of central nervous system agents and selective receptor ligands. Commonly employed in research settings for the construction of more complex amine-containing molecules due to its stability as a hydrochloride salt. Also utilized in asymmetric synthesis and catalysis where the toluidine backbone offers steri

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of active ingredients requiring chiral amine functionalities, particularly in the development of central nervous system agents and selective receptor ligands. Commonly employed in research settings for the construction of more complex amine-containing molecules due to its stability as a hydrochloride salt. Also utilized in asymmetric synthesis and catalysis where the toluidine backbone offers steric and electronic advantages.

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