5-MeO-DiPT

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Description

5-Methoxy-N,N-diisopropyltryptamine (5-MeO-DiPT) Research Chemical | CAS 101234-76-2 | Analytical Reference Standard
Introduction
5-Methoxy-N,N-diisopropyltryptamine, commonly abbreviated as 5-MeO-DiPT or fog, is a synthetic substituted tryptamine compound with the molecular formula C16H24N2O and a molar mass of 260.38 g/mol. This analytical reference standard is supplied for legitimate scientific research applications including chromatographic method development, forensic toxicology screening, and neuropharmacological studies investigating serotonin receptor binding profiles. As a structural analog combining the 5-methoxy substitution of 5-MeO-DMT with the N,N-diisopropyl substitution of DiPT, this compound serves as a valuable tool for analytical validation and structure-activity relationship research in controlled laboratory environments.
Key Features and Specifications
Chemical Name: 5-Methoxy-N,N-diisopropyltryptamine Synonyms: 5-MeO-DiPT, fog, 5-methoxy-N,N-diisopropyl tryptamine, 3-[2-(diisopropylamino)ethyl]-5-methoxy-1H-indole CAS Number: 101234-76-2 (free base); salt forms may have distinct identifiers Molecular Formula: C16H24N2O Molecular Weight: 260.38 g/mol Purity: Greater than or equal to 98 percent by HPLC for analytical reference standards Physical Form: Crystalline solid, powder, or solution depending on formulation Solubility: Soluble in DMSO, methanol, ethanol, and chloroform; limited solubility in aqueous buffers at neutral pH Storage Conditions: Store at minus 20 degrees Celsius in airtight, light-resistant container under inert atmosphere Stability: Sensitive to oxidation and light; prepare fresh solutions for analytical use; protect from moisture Analytical Data: UV absorption maxima at approximately 220 nm, 275 nm, and 285 nm; identity confirmed by NMR, LC-MS, and FTIR spectroscopy; melting point varies by salt form
Applications
This product is intended exclusively for laboratory research and forensic analytical applications. Legitimate use cases include: development and validation of LC-MS, GC-MS, and HPLC analytical methods for tryptamine detection; forensic toxicology reference material for identification and quantification of novel psychoactive substances; in vitro receptor binding and functional assays studying 5-HT1A, 5-HT2A, and 5-HT7 serotonin receptor pharmacology; quality control calibration standards for analytical instrumentation; academic research on structure-activity relationships within the 5-methoxy substituted tryptamine chemical class; metabolic stability studies using liver microsome or hepatocyte models. This compound is utilized as an analytical reference standard in research settings investigating serotonergic compound detection, metabolism, and receptor interaction mechanisms.
Safety and Handling
Handle only in a properly equipped chemical laboratory with appropriate engineering controls and institutional approval. Required personal protective equipment includes nitrile or chemical-resistant gloves, safety goggles or face shield, laboratory coat, and respiratory protection when handling powders or aerosols. Use only within a certified chemical fume hood to minimize inhalation exposure. Avoid skin contact, eye contact, and ingestion. This compound may cause irritation to skin, eyes, and respiratory tract. In case of contact, flush affected area with water for at least 15 minutes and seek medical attention. Store separately from oxidizing agents, strong acids, and light sources. Dispose of waste according to institutional hazardous chemical protocols and local environmental regulations. Refer to the Safety Data Sheet (SDS) for comprehensive hazard classification, first aid measures, fire-fighting procedures, and emergency response information.
Regulatory and Compliance Information
5-MeO-DiPT is subject to varying legal classifications across jurisdictions. In the United Kingdom, it is classified as a Class A controlled substance under the Misuse of Drugs Act. In Germany, it is regulated under the NpSG for industrial and scientific use only. In several European Union member states and other countries including Canada and Australia, it is controlled under new psychoactive substance legislation. In the United States, while not explicitly scheduled at the federal level, it may be considered a controlled substance analogue under the Federal Analogue Act if intended for human consumption. Researchers and purchasers are solely responsible for verifying compliance with all applicable local, state, national, and institutional regulations prior to ordering, possessing, importing, or using this material. This product is not approved by any regulatory agency for diagnostic, therapeutic, veterinary, or human consumption purposes.
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