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N-(3-FLUOROPHENYLMETHYL)PROPYLAMINE, also known as 3-FPM, is a synthetic amine compound characterized by the presence of a fluorine atom and an aromatic phenyl group. It is primarily recognized as a research chemical and has not been approved for medical applications. 3-FPM functions as a selective dopamine and norepinephrine reuptake inhibitor, which leads to elevated levels of these neurotransmitters in the brain, potentially causing stimulating and euphoric effects. However, its use is associated with risks of negative side effects and potential long-term health implications, as its safety profile and effects on the human body are not comprehensively understood. Given its potential for abuse and the absence of regulatory approval, 3-FPM is classified as a controlled substance in numerous jurisdictions.

90389-86-9

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90389-86-9 Usage

Uses

Used in Research Applications:
3-FPM is utilized as a research chemical for studying the effects of selective dopamine and norepinephrine reuptake inhibition on neurotransmitter levels in the brain. This helps scientists to better understand the mechanisms of action and potential therapeutic applications related to these neurotransmitters.
Used in Pharmaceutical Development:
Although not approved for medical use, 3-FPM may be explored in the development of pharmaceuticals targeting conditions related to dopamine and norepinephrine imbalances. Its mechanism of action could provide insights into the development of new treatments for neurological and psychiatric disorders.
Used in Controlled Substances Regulation:
Due to its potential for abuse and the lack of comprehensive safety data, 3-FPM is used as a case study in the regulation of controlled substances. Its classification and control measures can inform the development of policies and guidelines for the management of similar compounds in the future.

Check Digit Verification of cas no

The CAS Registry Mumber 90389-86-9 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 90389-86:
(7*9)+(6*0)+(5*3)+(4*8)+(3*9)+(2*8)+(1*6)=159
159 % 10 = 9
So 90389-86-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H14FN/c1-2-6-12-8-9-4-3-5-10(11)7-9/h3-5,7,12H,2,6,8H2,1H3

90389-86-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H56794)  3-Fluoro-N-n-propylbenzylamine, 97%   

  • 90389-86-9

  • 250mg

  • 1470.0CNY

  • Detail
  • Alfa Aesar

  • (H56794)  3-Fluoro-N-n-propylbenzylamine, 97%   

  • 90389-86-9

  • 1g

  • 4704.0CNY

  • Detail

90389-86-9SDS

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-(3-Fluorobenzyl)propan-1-amine

1.2 Other means of identification

Product number -
Other names N-(3-Fluorobenzyl)-1-propanamine

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:90389-86-9 SDS

90389-86-9Upstream product

90389-86-9Downstream Products

90389-86-9Relevant 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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