Etilamfetamine hydrochloride

Base Information

• Chemical Name: Etilamfetamine hydrochloride
• CAS No.: 16105-78-5
• Molecular Formula: C11H17 N . Cl H
• Molecular Weight: 199.724
• Hs Code.: 2921499090
• European Community (EC) Number: 240-270-9
• NSC Number: 54938,39705
• UNII: ZD9V2BK5GY
• DSSTox Substance ID: DTXSID90936445
• Wikidata: Q27295344
• ChEMBL ID: CHEMBL1976895
• Mol file: 16105-78-5.mol

Synonyms:ethylamphetamine;ethylamphetamine hydrochloride;ethylamphetamine hydrochloride, (+-)-isomer;ethylamphetamine hydrochloride, (R)-isomer;ethylamphetamine, (R)-isomer;N-ethylamphetamine

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

Chemical Property of Etilamfetamine hydrochloride

Chemical Property:

• Boiling Point: 235.3°Cat760mmHg
• Flash Point: 95.5°C
• PSA: 12.03000
• Density: g/cm³
• LogP: 3.42000
• Storage Temp.: 2-8°C
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 199.1127773
• Heavy Atom Count: 13
• Complexity: 106

Purity/Quality:

Safty Information:

• Pictogram(s): Xn,T,F
• Hazard Codes: Xn,T,F
• Statements: 22-39/23/24/25-23/24/25-11
• Safety Statements: 7-16-36/37-45

MSDS Files:

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCNC(C)CC1=CC=CC=C1.Cl
• Description: N-Ethylamphetamine (EMA) is an N-substituted amphetamine with an ethyl group on the amphetamine backbone. As a stimulant drug of the phenethylamine and amphetamine chemical classes, it is widely known as an anorectic marketed under the tradename Apetinil?. EMA has been abused as a “designer drug” alternative to amphetamine and possibly methamphetamine. This product is intended for forensic or research purposes.

Technology Process of Etilamfetamine hydrochloride

There total 1 articles about Etilamfetamine 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: 88.0%

ethylamine (75-04-7,85404-22-4) + 1-phenyl-acetone (103-79-7,136675-26-8) → dl-N-ethylamphetamine hydrochloride (16105-78-5,1858-47-5,26194-85-4,26194-77-4)

Guidance literature:

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

DOI:10.1080/004982599238344

upstream raw materials:

ethylamine

1-phenyl-acetone

Refernces