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51553-17-4

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51553-17-4 Usage

Description

2-(Ethylamino)propiophenone hydrochloride, also known as N-Ethylcathinone or ethylpropion, is an amphetamine and stimulant drug. It is a cathinone derivative that produces amphetamine-like stimulus effects. This white solid is commonly found in illicit drug markets, often sold under street names such as ETH-CAT. It is also used as a starting material in calibrators and controls for various testing applications, including forensic analysis, urine drug testing, and clinical toxicology.

Uses

Used in Illicit Drug Market:
2-(Ethylamino)propiophenone hydrochloride is used as a recreational drug for its amphetamine-like stimulus effects. It is often sold alongside mephedrone as "ecstasy" at parties and raves, as well as in bath salt blends across the US, Europe, and Australia.
Used in Forensic Analysis:
2-(Ethylamino)propiophenone hydrochloride is used as a starting material in calibrators and controls for Gas Chromatography/Mass Spectrometry (GC/MS) or Liquid Chromatography/Mass Spectrometry (LC/MS) bath salt testing applications. This helps in the identification and quantification of the drug in forensic investigations.
Used in Urine Drug Testing:
2-(Ethylamino)propiophenone hydrochloride is utilized as a reference material in urine drug testing to ensure the accuracy and reliability of test results. It helps in the development and validation of testing methods for detecting the presence of the drug in urine samples.
Used in Clinical Toxicology:
2-(Ethylamino)propiophenone hydrochloride is used in the development of testing protocols and procedures for clinical toxicology. It aids in the identification and quantification of the drug in biological samples, which is crucial for understanding its toxic effects and potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 51553-17-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,5 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51553-17:
(7*5)+(6*1)+(5*5)+(4*5)+(3*3)+(2*1)+(1*7)=104
104 % 10 = 4
So 51553-17-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO.ClH/c1-3-12-9(2)11(13)10-7-5-4-6-8-10;/h4-9,12H,3H2,1-2H3;1H

51553-17-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Ethylamino)propiophenone Hydrochloride

1.2 Other means of identification

Product number -
Other names 2-(ethylamino)-1-phenylpropan-1-one,hydrochloride

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:51553-17-4 SDS

51553-17-4Relevant articles and documents

The analysis of amphetamine-like cathinone derivatives using positive electrospray ionization with in-source collision-induced dissociation

Power, John D.,McDermott, Seán D.,Talbot, Brian,O'Brien, John E.,Kavanagh, Pierce

, p. 2601 - 2611 (2013/01/15)

Rationale: Amphetamine-like cathinone derivatives have become popular as recreational drugs over the past several years but their identification for forensic purposes is made difficult as they undergo extensive fragmentation under commonly used electron ionization (EI) conditions to afford ambiguous mass spectra. To overcome this, the feasibility of using positive electrospray ionization (ESI) with in-source collision-induced dissociation (CID) to produce distinguishable product ion mass spectra was examined. Methods: A set of six homologous cathinone derivatives was analyzed using an LTQ/Orbitrap high-resolution mass spectrometer to establish if there are any commonalities or uniqueness in their mass spectra. These compounds and a number of other cathinone derivatives were also analyzed on a single quadrupole mass spectrometer to establish the feasibility of using in-source CID for their identification in forensic drug samples. Results: The ESI product ion mass spectra of the [M + H]+ ions of six model compounds were found to be readily interpretable and product ion formation pathways are presented. The use of such mass spectral data in the analysis of forensic drug samples facilitated the discrimination of closely related cathinone derivatives that were difficult to distinguish using conventional gas chromatography/electron ionization mass spectrometry. A product ion mass spectral library of 22 commonly encountered cathinone derivatives was also developed. Conclusions: It has been shown that the product ion ESI mass spectra of cathinone derivatives are readily interpretable and are useful for the identification of this drug group in forensic samples. Copyright