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93963-24-7

N-ethyl-p-methoxy-alpha-methylphenethylamine hydrochloride, also known as N-ethyl-4-Methoxyamphetamine (EMA), is an analog of 4-MA. It is a compound with a decreased analgesic potency due to the addition of an N-ethyl substituent. The other physiological and toxicological properties of this compound are not known. It is primarily intended for forensic and research applications.
Used in Forensic Applications:
N-ethyl-p-methoxy-alpha-methylphenethylamine hydrochloride is used as a forensic tool for the identification and analysis of this compound in various samples, such as biological fluids and tissues, to aid in investigations and legal proceedings.
Used in Research Applications:
N-ethyl-p-methoxy-alpha-methylphenethylamine hydrochloride is used as a research chemical to study its properties, effects, and potential applications in the scientific community. This may include investigations into its interactions with biological systems, its potential therapeutic uses, and its role as an analog of other compounds.
Used in Pharmaceutical Development:
As an analog of the CNS stimulant Amphetamine, N-ethyl-p-methoxy-alpha-methylphenethylamine hydrochloride is used in the development of new pharmaceuticals with increased analgesic effects. This may involve testing its efficacy and safety in preclinical and clinical trials, as well as exploring its potential synergistic effects with other drugs.
Note: N-ethyl-p-methoxy-alpha-methylphenethylamine hydrochloride is classified as a controlled substance, which may impose certain restrictions and regulations on its use, production, and distribution.

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  • 93963-24-7 Structure

  • Basic information

    1. Product Name: N-ethyl-p-methoxy-alpha-methylphenethylamine hydrochloride
    2. Synonyms: N-ethyl-p-methoxy-alpha-methylphenethylamine hydrochloride;N-Ethyl-1-(4-methoxyphenyl)propan-2-amine hydrochloride;N-Ethyl-4-Methoxy AMphetaMine Hydrochloride;Ethyl[1-(4-methoxyphenyl)propan-2-yl]amine hydrochloride;N-Ethyl-N-[2-(4-methoxyphenyl)-1-methylethyl]amine hydrochloride;(±)-N-Ethyl-p-MethoxyaMphetaMine Hydrochloride;N-Ethyl-4-Methoxy-α-MethylbenzeneethanaMine Hydrochloride;N-Ethyl-p-Methoxy-α-MethylphenethylaMine Hydrochloride
    3. CAS NO:93963-24-7
    4. Molecular Formula: C12H19NO*ClH
    5. Molecular Weight: 229.7463
    6. EINECS: 300-765-3
    7. Product Categories: APIS;Amines;Aromatics;Drug Analogues;Intermediates & Fine Chemicals;Pharmaceuticals
    8. Mol File: 93963-24-7.mol

  • Chemical Properties

    1. Melting Point: 156-157 °C
    2. Boiling Point: 280.6 °C at 760 mmHg
    3. Flash Point: 116.1 °C
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. Water Solubility: very faint turbidity in Water
    10. CAS DataBase Reference: N-ethyl-p-methoxy-alpha-methylphenethylamine hydrochloride(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-ethyl-p-methoxy-alpha-methylphenethylamine hydrochloride(93963-24-7)
    12. EPA Substance Registry System: N-ethyl-p-methoxy-alpha-methylphenethylamine hydrochloride(93963-24-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 93963-24-7(Hazardous Substances Data)

93963-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93963-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,6 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 93963-24:
(7*9)+(6*3)+(5*9)+(4*6)+(3*3)+(2*2)+(1*4)=167
167 % 10 = 7
So 93963-24-7 is a valid CAS Registry Number.

93963-24-7 Well-known Company Product Price

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  • TCI America

  • (E0387)  2-Ethylamino-1-(4-methoxyphenyl)propane Hydrochloride  >98.0%(T)

  • 93963-24-7

  • 25g

  • 1,200.00CNY

  • Detail

93963-24-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-1-(4-methoxyphenyl)propan-2-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-methoxy-N-ethylamphetamine 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:93963-24-7 SDS

93963-24-7Relevant articles and documents

Involvement of CYP2D6 in the in vitro metabolism of amphetamine, two N-alkylamphetamines and their 4-methoxylated derivatives

Bach, Mimi V.,Coutts,Baker

, p. 719 - 732 (2007/10/03)

1. Amphetamine (AM) and five amphetamine derivatives, N-ethylamphetamine (NEA), N-butylamphetamine (NBA), 4-methoxyamphetamine (M-AM), 4-methoxy-N-ethylamphetamine (M-NEA) and 4-methoxy-N-butylamphetamine (M-NBA) were incubated with microsomal preparations from cells expressing human CYP2D6 to determine whether the enzyme was capable of catalyzing the direct ring oxidation of all substrates; the N-dealkylation of NEA, NBA, M-NEA and M-NBA; and the O-demethylation of M-AM, M-NEA and M-NBA. 2. None of the six compounds examined was N-dealkylated to any extent. 3. The only metabolites produced from AM, NEA and NBA were the corresponding ring 4-hydroxylated compounds, and the rates of formation were low. 4. All ring 4-methoxylated substrates were efficiently O-demethylated by CYP2D6 to their corresponding phenols. The size of the N-alkyl group influenced the rates of formation of these phenolamines. In contrast to reported findings with 2- and 3-methoxyamphetamines, none of the 4-methoxyamphetamines was ring-oxidized in the CYP2D6 enzyme system to 2- or 3-hydroxy-4-methoxyamphetamines or to dihydroxy-amphetamines.

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