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3,4-Methylenedioxymethamphetamine (MDMA), commonly known as ecstasy (tablet form), and molly (crystal form),[19][20] is an entactogen with stimulant and minor psychedelic properties.[17][21][22]
MDMA was first synthesized in 1912 by Merck chemist Anton Köllisch.[23] It was used to enhance psychotherapy beginning in the 1970s and became popular as a street drug in the 1980s.[24][25] MDMA is commonly associated with dance parties, raves, and electronic dance music.[26] Tablets sold as ecstasy may be mixed with other substances such as ephedrine, amphetamine, and methamphetamine.[24] In 2016, about 21 million people between the ages of 15 and 64 used ecstasy (0.3% of the world population).[27] In the United States, as of 2017, about 7% of people have used MDMA at some point in their lives and 0.9% have used it in the last year.[28] The lethal risk from one dose of MDMA is estimated to be from 1 death in 20,000 instances to 1 death in 50,000 instances.
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The purported pharmacological effects that may be prosocial include altered sensations, increased energy, empathy, and pleasure.[22][24] When taken by mouth, effects begin in 30 to 45 minutes and last three to six hours.[13][25] Short-term adverse effects include grinding of the teeth, blurred vision, sweating, and a rapid heartbeat,[24] and extended use can also lead to addiction, memory problems, paranoia, and difficulty sleeping. Deaths have been reported due to increased body temperature and dehydration. MDMA acts primarily by increasing the release of the neurotransmitters serotonin, dopamine, and norepinephrine in parts of the brain.[24][25] It belongs to the substituted amphetamine classes of drugs.[10][30] MDMA is structurally similar to mescaline (a psychedelic), methamphetamine (a stimulant), as well as endogenous monoamine neurotransmitters such as serotonin, norepinephrine, and dopamine.[31]
MDMA has limited approved medical uses in a small number of countries,[32] but is illegal in most jurisdictions.[33] MDMA-assisted psychotherapy is a promising and generally safe treatment for post-traumatic stress disorder when administered in controlled therapeutic settings.[34][35] In the United States, the Food and Drug Administration (FDA) has given MDMA breakthrough therapy status (though there no current clinical indications in the US).[36] Canada has allowed limited distribution of MDMA upon application to and approval by Health Canada.[37] In Australia, it may be prescribed in the treatment of PTSD by specifically authorised psychiatrists.[38]
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MDMA is often considered the drug of choice within the rave culture and is also used at clubs, festivals, and house parties.[15] In the rave environment, the sensory effects of music and lighting are often highly synergistic with the drug. The psychedelic amphetamine quality of MDMA offers multiple appealing aspects to users in the rave setting. Some users enjoy the feeling of mass communion from the inhibition-reducing effects of the drug, while others use it as party fuel because of the drug’s stimulatory effects.[39] MDMA is used less often than other stimulants, typically less than once per week.[40]
MDMA is sometimes taken in conjunction with other psychoactive drugs such as LSD,[41] psilocybin mushrooms, 2C-B, and ketamine. The combination with LSD is called “candy-flipping”.[41] The combination with 2C-B is called “nexus flipping”. For this combination, most people take the MDMA first, wait until the peak is over, and then take the 2C-B.[42]
MDMA is often co-administered with alcohol, methamphetamine, and prescription drugs such as SSRIs with which MDMA has several drug-drug interactions.[43][44][45] Three life-threatening reports of MDMA co-administration with ritonavir have been reported;[46] with ritonavir having severe and dangerous drug-drug interactions with a wide range of both psychoactive, anti-psychotic, and non-psychoactive drugs.[47]
Medical
As of 2023, MDMA therapies have only been approved for research purposes, with no widely accepted medical indications,[10][48][49] although this varies by jurisdiction. Before it was widely banned, it saw limited use in psychotherapy.[8][10][50] In 2017 the United States Food and Drug Administration (FDA) granted breakthrough therapy designation for MDMA-assisted psychotherapy for post-traumatic stress disorder (PTSD).[51][52]
Some researchers have proposed that psychedelics in general may act as active “super placebos” used for therapeutic purposes.[53][54]
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| Specification | Detail |
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| Chemical Name | 3,4-Methylenedioxymethamphetamine |
| Common Names | MDMA, Ecstasy, Molly |
| Chemical Formula | C11H15NO2 |
| CAS Number | 42542-10-9 (HCl salt) |
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| Characteristic | Detail |
|---|---|
| Chemical Name | 3,4-Methylenedioxymethamphetamine |
| Common Name | MDMA, Ecstasy |
| Chemical Formula | C11H15NO2 |
| CAS Number | 42542-10-9 |
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3,4-Methylenedioxymethamphetamine (MDMA), commonly known as ecstasy (tablet form), and molly (crystal form),[19][20] is an entactogen with stimulant and minor psychedelic properties.[17][21][22]
MDMA was first synthesized in 1912 by Merck chemist Anton Köllisch.[23] It was used to enhance psychotherapy beginning in the 1970s and became popular as a street drug in the 1980s.[24][25] MDMA is commonly associated with dance parties, raves, and electronic dance music.[26] Tablets sold as ecstasy may be mixed with other substances such as ephedrine, amphetamine, and methamphetamine.[24] In 2016, about 21 million people between the ages of 15 and 64 used ecstasy (0.3% of the world population).[27] In the United States, as of 2017, about 7% of people have used MDMA at some point in their lives and 0.9% have used it in the last year.[28] The lethal risk from one dose of MDMA is estimated to be from 1 death in 20,000 instances to 1 death in 50,000 instances.[29]
The purported pharmacological effects that may be prosocial include altered sensations, increased energy, empathy, and pleasure.[22][24] When taken by mouth, effects begin in 30 to 45 minutes and last three to six hours.[13][25] Short-term adverse effects include grinding of the teeth, blurred vision, sweating, and a rapid heartbeat,[24] and extended use can also lead to addiction, memory problems, paranoia, and difficulty sleeping. Deaths have been reported due to increased body temperature and dehydration. MDMA acts primarily by increasing the release of the neurotransmitters serotonin, dopamine, and norepinephrine in parts of the brain.[24][25] It belongs to the substituted amphetamine classes of drugs.[10][30] MDMA is structurally similar to mescaline (a psychedelic), methamphetamine (a stimulant), as well as endogenous monoamine neurotransmitters such as serotonin, norepinephrine, and dopamine.[31]
MDMA has limited approved medical uses in a small number of countries,[32] but is illegal in most jurisdictions.[33] MDMA-assisted psychotherapy is a promising and generally safe treatment for post-traumatic stress disorder when administered in controlled therapeutic settings.[34][35] In the United States, the Food and Drug Administration (FDA) has given MDMA breakthrough therapy status (though there no current clinical indications in the US).[36] Canada has allowed limited distribution of MDMA upon application to and approval by Health Canada.[37] In Australia, it may be prescribed in the treatment of PTSD by specifically authorised psychiatrists.[38]
Uses
Recreational
MDMA is often considered the drug of choice within the rave culture and is also used at clubs, festivals, and house parties.[15] In the rave environment, the sensory effects of music and lighting are often highly synergistic with the drug. The psychedelic amphetamine quality of MDMA offers multiple appealing aspects to users in the rave setting. Some users enjoy the feeling of mass communion from the inhibition-reducing effects of the drug, while others use it as party fuel because of the drug’s stimulatory effects.[39] MDMA is used less often than other stimulants, typically less than once per week.[40]
MDMA is sometimes taken in conjunction with other psychoactive drugs such as LSD,[41] psilocybin mushrooms, 2C-B, and ketamine. The combination with LSD is called “candy-flipping”.[41] The combination with 2C-B is called “nexus flipping”. For this combination, most people take the MDMA first, wait until the peak is over, and then take the 2C-B.[42]
MDMA is often co-administered with alcohol, methamphetamine, and prescription drugs such as SSRIs with which MDMA has several drug-drug interactions.[43][44][45] Three life-threatening reports of MDMA co-administration with ritonavir have been reported;[46] with ritonavir having severe and dangerous drug-drug interactions with a wide range of both psychoactive, anti-psychotic, and non-psychoactive drugs.[47]
Medical
As of 2023, MDMA therapies have only been approved for research purposes, with no widely accepted medical indications,[10][48][49] although this varies by jurisdiction. Before it was widely banned, it saw limited use in psychotherapy.[8][10][50] In 2017 the United States Food and Drug Administration (FDA) granted breakthrough therapy designation for MDMA-assisted psychotherapy for post-traumatic stress disorder (PTSD).[51][52]
Some researchers have proposed that psychedelics in general may act as active “super placebos” used for therapeutic purposes.
What is MDMA (3,4-methylenedioxymethamphetamine)
MDMA (3,4-methylenedioxymethamphetamine) is a synthetic drug that acts as both a stimulant and a psychedelic. It is commonly known as ecstasy when in pill form and molly when in crystal or powder form.
It alters mood and perception, producing feelings of increased energy, pleasure, emotional warmth, and deep connection with others.
3,4-Methylenedioxymethamphetamine (MDMA), commonly known as ecstasy in tablet form, and molly in crystal form, is an entactogen with stimulant and minor psychedelic properties.
MDMA was first synthesized in 1912 by Merck chemist Anton Köllisch. It was used to enhance psychotherapy beginning in the 1970s and became popular as a street drug in the 1980s.
MDMA is commonly used by attendees of dance parties, raves, and electronic dance music festivals. Tablets sold as ecstasy may be mixed with other substances such as ephedrine, amphetamine, and methamphetamine.
The lethal risk from one dose of MDMA is estimated to be from 1 death in 20,000 instances to 1 death in 50,000 instances.
The purported pharmacological effects that may be prosocial include altered sensations, increased energy, empathy, and pleasure. When taken by mouth, effects begin in 30 to 45 minutes and last three to six hours.
Short-term adverse effects include bruxism, blurred vision, sweating, and tachycardia, and extended use can also lead to addiction, amnesia, memory disorders, paranoia, and insomnia. Deaths have been reported due to increased body temperature and dehydration.
MDMA acts primarily by increasing the release of the neurotransmitters serotonin, dopamine, and norepinephrine in parts of the brain. It belongs to the substituted amphetamine classes of drugs.
![]()
MDMA is structurally similar to mescaline (a psychedelic), methamphetamine (a stimulant), as well as endogenous monoamine neurotransmitters such as serotonin, norepinephrine, and dopamine.
MDMA has limited approved medical uses in a small number of countries, but is illegal in most jurisdictions.
MDMA-assisted psychotherapy may substantially improve PTSD symptoms, response, and remission rates compared to psychotherapy alone, but the evidence is low to very low certainty and safety data are limited, with some increased transient adverse events.
In the United States, the Food and Drug Administration (FDA) has given MDMA breakthrough therapy status (though there are no current clinical indications in the US).
Canada has allowed limited distribution of MDMA upon application to and approval by Health Canada.In Australia, it may be prescribed in the treatment of PTSD by specifically authorised psychiatrists.
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Others
Alternate Names: MDMA, Midomafetamine, 1,3-Benzodioxole-5-ethanamine, N,alpha-dimethyl-, Ecstasy (Drug), Molly
CAS No: 42542-10-9
PubChem CID: 1615
Mol Formula: C11H15NO2
Mol Weight: 193.24 g/mol
Controlled Drug Substance: Yes (Schedule I)
IUPAC Name: 1-(1,3-benzodioxol-5-yl)-N-methylpropan-2-amine
Therapeutic use: Psychedelics
Drug Class: Schedule I controlled substances
Commercial / Development Status: Clinical APIs
Source / Manufacturing Origin: Synthetic APIs
API Description: 3,4-methylenedioxymethamphetamine is a DEA Schedule I controlled substance. Substances in the DEA Schedule I have no currently accepted medical use in the United States, a lack of accepted safety for use under medical supervision, and a high potential for abuse. It is a Hallucinogenic substances substance.

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Small doses of MDMA are used by some religious practitioners as an entheogen to enhance prayer or meditation.[55] MDMA has been used as an adjunct to New Age spiritual practices
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3,4-METHYLENEDIOXYMETHAMPHETAMINE | 42542-10-9
May 28, 2026 · (+/-)-3,4-METHYLENEDIOXYMETHAMPHETAMINE (CAS 42542-10-9) information, including chemical properties, …
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Boiling point: bp0.4 100-110°
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Flash point: 9℃
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Density: 1.100±0.06 g/cm3 (Predicted)
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3,4-Methylenedioxymethamphetamine
Base Information- Chemical Name:3,4-Methylenedioxymethamphetamine
- CAS No.:42542-10-9
- Deprecated CAS:69610-10-2,54946-52-0
- Molecular Formula:C11H15NO2
- Molecular Weight:193.246
- Hs Code.:2932999099
- UNII:KE1SEN21RM
- DSSTox Substance ID:DTXSID90860791
- Nikkaji Number:J276.360E
- Wikipedia:MDMA
- Wikidata:Q69488
- NCI Thesaurus Code:C61081
- Pharos Ligand ID:QSU2N2ZPKBBG
- Metabolomics Workbench ID:52856
- ChEMBL ID:CHEMBL43048
- Mol file:42542-10-9.mol
Synonyms:Ecstasy (Drug);Hydrochloride, N-Methyl-3,4-methylenedioxyamphetamine;MDMA;Methylenedioxymethamphetamine;N Methyl 3,4 methylenedioxyamphetamine;N Methyl 3,4 methylenedioxyamphetamine Hydrochloride;N-Methyl-3,4-methylenedioxyamphetamine;N-Methyl-3,4-methylenedioxyamphetamine Hydrochloride
This product is a nationally controlled contraband, and the Lookchem platform doesn’t provide relevant sales information.Chemical Property of 3,4-MethylenedioxymethamphetamineChemical Property:- Vapor Pressure:0.000272mmHg at 25°C
- Boiling Point:283.39 °C at 760 mmHg
- PKA:10.32±0.10(Predicted)
- Flash Point:113.23 °C
- PSA:30.49000
- Density:1.1 g/cm3
- LogP:1.95660
- Storage Temp.:2-8°C
- XLogP3:2.2
- Hydrogen Bond Donor Count:1
- Hydrogen Bond Acceptor Count:3
- Rotatable Bond Count:3
- Exact Mass:193.110278721
- Heavy Atom Count:14
- Complexity:186
- Purity/Quality:
Safty Information:- Pictogram(s):F,T
- Hazard Codes:F,T
- Statements:11-23/24/25-39/23/24/25
- Safety Statements:7-16-36/37-45
Useful:- Canonical SMILES:CC(CC1=CC2=C(C=C1)OCO2)NC
- Recent ClinicalTrials:Randomized Placebo-controlled Study of MDMA-assisted Therapy in People With PTSD – Israel
- Recent EU Clinical Trials:An Open- Label, Phase 2, Multicenter Feasibility Study if Manualized MDMA-Assisted Psychotherapy with an fMRI sub-study Assessing Changes in Brain Activity in Subjects with Posttraumatic Stress Disorder.
Technology Process of 3,4-MethylenedioxymethamphetamineThere total 19 articles about 3,4-Methylenedioxymethamphetamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:Reference yield: 85.0%
- Guidance literature:
-
With lithium aluminium tetrahydride; In tetrahydrofuran; for 4h; Reflux;
Reference yield: 78.0%
- Guidance literature:
-
1-(1,3-benzodioxol-5-yl)-2-propanone; methylamine; In ethanol; water; at 20 ℃; for 1h;With hydrogen; platinum(IV) oxide; In ethanol; water; for 3.5h; under 2896.11 Torr; Further stages.;
Reference yield:
- Guidance literature:
-
With lithium aluminium tetrahydride; In diethyl ether; for 4h; Yield given; Heating;
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Boiling point: bp0.4 100-110°
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Flash point: 9℃
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Density: 1.100±0.06 g/cm3 (Predicted)
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