42542-07-4

Basic information

• Product Name: 1-(3,4-Methylenedioxyphenyl)-2-butanamine
• Synonyms: 3,4-Methylenedioxy-α-ethyl-β-phenylethylaMine Hydrochloride;α-Ethyl-1,3-benzodioxole-5-ethanaMine Hydrochloride;(±)-BDB hydrochloride solution;3,4-Methylenedioxyphenyl-2-butanamine hydrochloride solution;1-(1,3-BENZODIOXOL-5-YL)-2-BUTANAMIN;1-(1,3-BENZODIOXOL-5-YL)-2-BUTANAMIN, >99% (HPLC);1-(1,3-Benzodioxol-5-yl)butan-2-amine;1-(3,4-Methylenedioxyphenyl)-2-butanamine
• CAS NO: 42542-07-4
• Molecular Formula: C11H15NO2
• Molecular Weight: 193.24
• EINECS: 200-659-6
• Product Categories: Amines;Aromatics;Heterocycles
• Mol File: 42542-07-4.mol
• Article Data: 0

Chemical Properties

• Melting Point: 152-154 °C
• Boiling Point: 297.3°Cat760mmHg
• Flash Point: 145.5°C
• Appearance: white/
• Density: 1.133g/cm³
• Vapor Pressure: 0.00136mmHg at 25°C
• Storage Temp.: ?20°C
• Solubility: H2O: soluble
• CAS DataBase Reference: 1-(3,4-Methylenedioxyphenyl)-2-butanamine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3,4-Methylenedioxyphenyl)-2-butanamine(42542-07-4)
• EPA Substance Registry System: 1-(3,4-Methylenedioxyphenyl)-2-butanamine(42542-07-4)

Safety Data

• Hazard Codes: Xn,T,F
• Statements: 20/21/22-39/23/24/25-23/24/25-11
• Safety Statements: 36-45-36/37-16-7
• RIDADR: UN 2811 6.1 / PGII
• Hazardous Substances Data: 42542-07-4(Hazardous Substances Data)

Usage

Description

1-(3,4-Methylenedioxyphenyl)-2-butanamine, also known as BDB, is a synthetic psychoactive substance belonging to the phenethylamine and amphetamine chemical classes. It is an analog of MDA, featuring an ethyl group in the alpha position. BDB is known for its ability to inhibit the reuptake of dopamine, serotonin, and norepinephrine, making it a compound of interest for forensic and research applications.

Uses

Used in Forensic Applications:
1-(3,4-Methylenedioxyphenyl)-2-butanamine is used as a forensic reference standard for the detection and identification of MDA and its analogs in criminal investigations. Its role in forensic science is crucial for understanding the chemical structure and properties of these substances, which aids in the development of detection methods and the analysis of evidence related to their use.
Used in Research Applications:
In the field of research, 1-(3,4-Methylenedioxyphenyl)-2-butanamine serves as a valuable tool for studying the mechanisms of action, pharmacology, and potential therapeutic applications of MDA and its analogs. By examining the interactions of BDB with neurotransmitter systems, researchers can gain insights into the effects of these substances on the brain and develop a better understanding of their potential risks and benefits.
Used in Drug Development:
1-(3,4-Methylenedioxyphenyl)-2-butanamine may also be utilized in the development of new drugs targeting the reuptake of dopamine, serotonin, and norepinephrine. By studying the structure-activity relationships of BDB and its effects on neurotransmitter systems, researchers can design and synthesize novel compounds with improved pharmacological profiles and potential therapeutic applications.
Used in Drug Delivery Systems:
Similar to gallotannin, 1-(3,4-Methylenedioxyphenyl)-2-butanamine could potentially be incorporated into drug delivery systems to enhance its bioavailability and therapeutic outcomes. By employing various organic and metallic nanoparticles as carriers, researchers can improve the delivery of BDB to target cells and tissues, potentially increasing its efficacy in specific applications.

InChI:InChI=1/C11H15NO2.ClH/c1-2-9(12)5-8-3-4-10-11(6-8)14-7-13-10;/h3-4,6,9H,2,5,7,12H2,1H3;1H