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N-[(3-fluorophenyl)methyl]ethanamine, commonly referred to as 3-FEA, is a psychoactive research chemical that belongs to the amphetamine class. It features a phenethylamine core and is structurally akin to other substituted amphetamines such as MDMA and 2C-B. Known for its stimulant and entactogenic properties, 3-FEA is utilized in recreational settings and by researchers interested in its effects on human physiology. However, due to potential health risks and the possibility of abuse, it has not been approved for medical use, necessitating adherence to legal and safety protocols in its handling and consumption.

90389-85-8

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90389-85-8 Usage

Uses

Used in Recreational Settings:
3-FEA is used as a recreational drug for its stimulant and entactogenic effects, providing users with heightened energy and a sense of emotional closeness.
Used in Scientific Research:
In the scientific community, 3-FEA serves as a research chemical, enabling scientists to study its impact on the human body and explore its potential applications in various fields of research.
Used in Pharmaceutical Development (hypothetical):
While not approved for medical use, 3-FEA could potentially be utilized in the development of pharmaceuticals targeting specific conditions, should future research reveal safe and effective applications.

Check Digit Verification of cas no

The CAS Registry Mumber 90389-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,8 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90389-85:
(7*9)+(6*0)+(5*3)+(4*8)+(3*9)+(2*8)+(1*5)=158
158 % 10 = 8
So 90389-85-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H12FN/c1-2-11-7-8-4-3-5-9(10)6-8/h3-6,11H,2,7H2,1H3

90389-85-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Ethyl-3-fluorobenzylamine

1.2 Other means of identification

Product number -
Other names N-[(3-fluorophenyl)methyl]ethanamine

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:90389-85-8 SDS

90389-85-8Upstream product

90389-85-8Relevant academic research and scientific papers

Benzylamines: Synthesis and evaluation of antimycobacterial properties

Meindl,Von Angerer,Schonenberger,Ruckdeschel

, p. 1111 - 1118 (2007/10/02)

The synthesis of benzylamines with various N-alkyl chains and substituents in the aromatic system as well as their evaluation on Mycobacterium tuberculosis H 37 Ra are described. The most active compounds in this test, N-methyl-3-chlorobenzylamine (MIC 10.2 μg/mL), N-methyl-3,5-dichlorobenzylamine (93, MIC 10.2 μg/mL), and N-butyl-3,5-difluorobenzylamine (MIC 6.4 μg/mL), also exhibited a marked inhibitory effect on Mycobacterium marinum and Mycobacterium lufu used for the determination of antileprotic properties. The combination of 93 with aminosalicylic acid, streptomycin, or dapsone exert marked supra-additive effects on M. tuberculosis H 37 Ra.

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