p-Methoxy-N,alpha-dimethylphenethylamine hydrochloride

Base Information

• Chemical Name: p-Methoxy-N,alpha-dimethylphenethylamine hydrochloride
• CAS No.: 3398-68-3
• Deprecated CAS: 6933-79-5,118931-17-2
• Molecular Formula: C11H17NO
• Molecular Weight: 215.723
• Hs Code.: 2922299090
• European Community (EC) Number: 222-265-3
• UNII: 0U3N9S2CHG
• DSSTox Substance ID: DTXSID00955561
• Wikidata: Q27237253
• Mol file: 3398-68-3.mol

Synonyms:(+-)-isomer of 4-methoxymethamphetamine;4-methoxymethamphetamine;4-methoxymethamphetamine hydrochloride;4-PMMA;HCl of 4-methoxymethamphetamine;HCl(+-)-isomer of 4-methoxymethamphetamine

 This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

Chemical Property of p-Methoxy-N,alpha-dimethylphenethylamine hydrochloride

Chemical Property:

• Melting Point: 174 °C
• Boiling Point: 262.9oC at 760 mmHg
• Flash Point: 9℃
• PSA: 21.26000
• LogP: 3.03850
• Storage Temp.: ?20°C
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 215.1076919
• Heavy Atom Count: 14
• Complexity: 130

Purity/Quality:

Safty Information:

• Hazard Codes: F,T
• Statements: 11-23/24/25-39/23/24/25
• Safety Statements: 16-36/37-45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(CC1=CC=C(C=C1)OC)NC.Cl
• Uses: The 4-methoxy analog of Methamphetamine (M258795). CNS stimulant. Controlled substance. The labelled 4-methoxy analog of Methamphetamine (M258795). CNS stimulant. Controlled substance.

Technology Process of p-Methoxy-N,alpha-dimethylphenethylamine hydrochloride

There total 1 articles about p-Methoxy-N,alpha-dimethylphenethylamine hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

4-methoxybenzyl methyl ketone (122-84-9) + methylamine (74-89-5) → 4-methoxy-N-methylamphetamine hydrochloride (3398-68-3)

Guidance literature:

With hydrogenchloride; hydrogen; platinum(IV) oxide; In ethanol; for 24h; under 1810.02 Torr;

DOI:10.1080/004982599238344

upstream raw materials:

4-methoxybenzyl methyl ketone

methylamine

Refernces