DPT (N,N-Dipropyltryptamine)

DPT (N,N-Dipropyltryptamine)

$135.00

25 in stock

SKU: SKU-6a3d3409bcd6d Category:

DPT is a synthetic tryptamine for psychopharmacological research. Purity ≥98% (HPLC). For research purposes only.

DPT (N,N-Dipropyltryptamine) is a crystalline psychedelic tryptamine derivative and structural analog of DMT synthesized strictly for analytical laboratory research, neurochemical profiling, and comparative receptor assays.
As a potent agonist at serotonin receptors (predominantly $5\text{-HT}_{1\text{A}}$ and $5\text{-HT}_{2\text{A}}$ subtypes), DPT (N,N-Dipropyltryptamine) serves as a vital reference standard for investigating receptor binding affinities, metabolic pathways, and mass spectrometry profiling. Every batch undergoes strict quality control testing to guarantee analytical purity, stability, and batch-to-batch consistency across scientific applications.

Chemical Specifications

  • Product Name: DPT (N,N-Dipropyltryptamine)
  • Chemical Name: N-[2-(1H-indol-3-yl)ethyl]-N-propylpropan-1-amine hydrochloride
  • CAS Number: 61-54-1 (base) / 16382-06-2 (HCl)
  • Molecular Formula: C16H24N2
  • Molecular Weight: 244.38 g/mol
  • Purity Standard: ≥98.0% (HPLC / GC-MS verified)
  • Physical Form: High-purity Crystalline Powder / Solid
  • Storage Recommendation: Store sealed in a cool, dry place (-20°C recommended) protected from direct sunlight, heat, and ambient moisture.

Laboratory & Research Applications

This tryptamine reference standard is designed for qualified scientific environments, including:
  1. High-Performance Liquid Chromatography (HPLC) assay calibration and quantitative testing.
  2. Gas Chromatography–Mass Spectrometry (GC-MS) qualitative identification.
  3. In vitro serotonin receptor binding affinity and receptor-ligand interaction assays.
Safety Notice: DPT (N,N-Dipropyltryptamine) is supplied strictly for authorized laboratory, analytical, and forensic research purposes only. This product is strictly not for human or veterinary consumption, in vivo diagnostic use, or therapeutic applications. Handle using standard personal protective equipment (PPE).
Weight 0.01 kg

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Product Name: DMT (N,N-Dimethyltryptamine) Synonyms: N,N-DMT; 2-(1H-indol-3-yl)-N,N-dimethylethanamine; Nigerine; Desoxybufotenine General Description: DMT is formally described as 2-(1H-indol-3-yl)-N,N-dimethylethanamine. It is a naturally occurring, highly potent psychedelic molecule belonging to the tryptamine class. DMT is found ubiquitously in nature across numerous plant species (such as Mimosa hostilis and Psychotria viridis, the latter being a primary component of the traditional Amazonian brew Ayahuasca) and is also produced endogenously in trace amounts within the mammalian nervous system. In analytical, clinical, and forensic toxicology, DMT is utilized as a fundamental reference standard. It is essential for the calibration of analytical instrumentation (such as LC-MS/MS, GC-MS, and HPLC) and the development of screening methodologies to identify and quantify the substance in botanical extracts, seized materials, or biological matrices. Technical Information (Freebase): CAS Number: 61-50-7 (Freebase) / 2031-64-1 (Fumarate salt) Molecular Formula: C12H16N2 Formula Weight: 188.27 g/mol SMILES: CN(C)CCC1=CNC2=CC=CC=C12 InChI Key: CNILEDYJOWOQHK-UHFFFAOYSA-N Formulation: Typically supplied as a neat crystalline solid (often formulated as a fumarate salt to ensure chemical stability, increased water solubility, and accurate dosing) or as a certified reference material solution (e.g., 1 mg/mL in methanol or acetonitrile). Biological Action: DMT acts primarily as a non-selective agonist at central serotonin receptors, particularly the 5-HT2A, 5-HT2C, and 5-HT1A subtypes. The robust activation of the 5-HT2A receptor is primarily responsible for its profound hallucinogenic effects. It also demonstrates affinity for the sigma-1 (σ1) receptor and the trace amine-associated receptor 1 (TAAR1). DMT is rapidly metabolized in the periphery by the enzyme monoamine oxidase A (MAO-A); consequently, it is largely inactive when administered orally unless co-ingested with an MAOI (such as the harmala alkaloids found in Banisteriopsis caapi). When vaporized or administered parenterally, it is characterized by an extremely rapid onset and a uniquely short duration of action. Regulatory and Safety Information: Intended Use: This product is intended strictly for use as an analytical reference standard for forensic, toxicological, and academic research purposes. Warning: This product is not for human or veterinary use. Legal Status: DMT is strictly controlled under international law (1971 Convention on Psychotropic Substances). In the United States, it is classified as a Schedule I Controlled Substance. Procurement of bulk solid material requires active Drug Enforcement Administration (DEA) registration or an equivalent national license. However, highly dilute solutions (e.g., 1 mg/mL in methanol) are often formulated and sold as DEA-exempt preparations to qualified diagnostic and forensic laboratories. Handling should only occur within professional laboratory environments using appropriate Personal Protective Equipment (PPE).

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If you want a **neutral, non-promotional description** of **MET**, you can use: **MET (N-methyl-N-ethyltryptamine)** is a synthetic tryptamine compound structurally related to other psychoactive tryptamines. It is generally described as a psychedelic substance that may affect perception, mood, and cognition. Formal human research on MET appears limited, and publicly available information on its pharmacology, toxicity, duration, long-term effects, and interaction profile is incomplete. As with other lesser-studied psychoactive compounds, potential risks may include unpredictable effects, adverse psychological reactions, and uncertainty about purity or composition in unregulated materials. Legal status may vary by jurisdiction. If you want, I can rewrite this as a: - **scientific catalog description** - **encyclopedia-style ent

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