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N,α,α’Trimethyldiphenethylamine is a chemical compound that is a derivative of amphetamine (A634340). It is known to possess psychostimulatory activities, which means it can stimulate the central nervous system and potentially influence mood, attention, and alertness.

53660-19-8

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53660-19-8 Usage

Uses

Used in Pharmaceutical Industry:
N,α,α’Trimethyldiphenethylamine is used as a psychostimulant for its ability to stimulate the central nervous system. Due to its amphetamine-like properties, it may have potential applications in the treatment of certain medical conditions that involve a lack of focus, attention, or energy.
Used in Research and Development:
N,α,α’Trimethyldiphenethylamine is also used in research and development for studying the effects of psychostimulants on the brain and behavior. Understanding its mechanisms of action can contribute to the development of new medications and therapies for various neurological and psychiatric disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 53660-19-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,6 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53660-19:
(7*5)+(6*3)+(5*6)+(4*6)+(3*0)+(2*1)+(1*9)=118
118 % 10 = 8
So 53660-19-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H25N/c1-16(14-18-10-6-4-7-11-18)20(3)17(2)15-19-12-8-5-9-13-19/h4-13,16-17H,14-15H2,1-3H3

53660-19-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-1-phenyl-N-(1-phenylpropan-2-yl)propan-2-amine

1.2 Other means of identification

Product number -
Other names N,Alpha,Alpha`-Trimethyldiphenethylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:53660-19-8 SDS

53660-19-8Downstream Products

53660-19-8Relevant academic research and scientific papers

Characterization of route specific impurities found in methamphetamine synthesized by the Leuckart and reductive amination methods

Kunalan, Vanitha,Daeid, Niamh Nic,Kerr, William J.,Buchanan, Hilary A. S.,McPherson, Allan R.

experimental part, p. 7342 - 7348 (2010/04/06)

Impurity profiling of seized methamphetamine can provide very useful information in criminal investigations and, specifically, on drug trafficking routes, sources of supply, and relationships between seizures. Particularly important is the identification of "route specific" impurities or those which indicate the synthetic method used for manufacture in illicit laboratories. Previous researchers have suggested impurities which are characteristic of the Leuckart and reductive amination (Al/Hg) methods of preparation. However, to date and importantly, these two synthetic methods have not been compared in a single study utilizing methamphetamine hydrochloride synthesized in-house and, therefore, of known synthetic origin. Using the same starting material, 1-phenyl-2-propanone (P2P), 40 batches of methamphetamine hydrochloride were synthesized by the Leuckart and reductive amination methods (20 batches per method). Both basic and acidic impurities were extracted separately and analyzed by GC/MS. From this controlled study, two route specific impurities for the Leuckart method and one route specific impurity for the reductive amination method are reported. The intra- and inter-batch variation of these route specific impurities was assessed. Also, the variation of the "target impurities" recently recommended for methamphetamine profiling is discussed in relation to their variation within and between production batches synthesized using the Leuckart and reductive amination routes.

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