5-MeO-MiPT 10mg Pellets

PRODUCT DESCRIPTION

Introduction

5-MeO-MiPT (5-Methoxy-N-methyl-N-isopropyltryptamine) is a synthetic tryptamine compound belonging to the class of indole alkylamines. It is a solid substance, often encountered in pellet form at specified dosages, such as 10mg pellets, for research use. Chemically, it is classified as a psychedelic tryptamine derivative and has been a focus of scientific and pharmacological interest since its first description by Alexander Shulgin in the mid-1980s. Its molecular structure features an indole backbone with methoxy substitution, lending to its distinct chemical and pharmacodynamic characteristics.

Chemical Properties and Specifications

2.1 Structural and Molecular Characteristics

• Chemical Formula: C15H22N2O

• Molecular Weight: 246.35 g/mol

• CAS Number: 96096-55-8

• IUPAC Name: 3-[2-(Methyl(isopropyl)amino)ethyl]-5-methoxy-1H-indole

• Synonyms:

  • 5-MeO-MiPT

  • 5-Methoxy-N-methyl-N-isopropyltryptamine

  • N-Isopropyl-N-methyl-5-methoxy-1H-indole-3-ethanamine

2.2 Physical Properties and Purity Standards

• Appearance: Light orange to dark orange solid pellets

• Purity: Typically ≥98% in research-grade samples

• Solubility: Slightly soluble in chloroform and methanol; sparingly soluble in water

• Storage Recommendations: Store at -20°C in a sealed container, protected from light and moisture to maintain stability

Pharmacological Profile and Mechanism of Action

3.1 Proposed Mechanism of Action

5-MeO-MiPT acts primarily as a non-selective agonist of serotonin receptors, especially the 5-HT2A receptor, which is implicated in psychedelic effects. It also binds to other serotonin receptor subtypes, including 5-HT1A and 5-HT2B, influencing complex neuropharmacological pathways. Additionally, 5-MeO-MiPT may inhibit serotonin and norepinephrine reuptake to a moderate extent, contributing to its psychoactive profile. The compound does not appear to significantly promote monoamine release.

3.2 Research Applications

5-MeO-MiPT serves as a tool for studying serotonergic systems and psychoactive tryptamines. It is used in research contexts exploring the binding affinities at various serotonin receptor subtypes and investigating molecular pharmacodynamics associated with psychedelic compounds. Its selective receptor profile makes it valuable for neurochemical and psychopharmacological research.

Comparative Analysis with Related Compounds

4.1 Compare to Related Compounds

5-MeO-MiPT is chemically related to other tryptamines such as 5-MeO-DiPT, MiPT, and 5-MeO-DMT. Unlike 5-MeO-DiPT, 5-MeO-MiPT is distinguished by an isopropyl group substitution rather than the diisopropyl groups, which imparts different receptor affinities and pharmacokinetics. Compared to MiPT, 5-MeO-MiPT contains a methoxy group at the 5-position of the indole ring, altering its interaction with serotonin receptors.

4.2 Advantages for Research

The compound’s distinct receptor binding profile and solubility make it suitable for in vitro and in vivo studies focusing on serotonin receptor pharmacology. Its relatively well-defined purity and standardized form factor (10mg pellets) facilitate reliable dosing and experimental reproducibility.

Safety and Handling Guidelines

5.1 Laboratory Safety

Handle 5-MeO-MiPT with appropriate personal protective equipment including gloves, lab coats, and eye protection. Use in a well-ventilated laboratory setting. Avoid inhalation, ingestion, and skin contact. Use proper tools to handle pellets to minimize direct contact. Follow all institutional guidelines for hazardous material handling.

5.2 Disposal and Environmental Considerations

Dispose of 5-MeO-MiPT waste according to local, state, and federal regulations for chemical waste. Do not release into the environment. Use designated chemical waste containers and work with environmental health and safety personnel for disposal.

5.3 Regulatory Status

Regulatory controls on 5-MeO-MiPT vary internationally. It is unscheduled federally in the United States but may be considered an analog under the Federal Analog Act. Some countries and jurisdictions have classified it under controlled substances, including the United Kingdom (Class A) and parts of China. Researchers should verify local regulations prior to acquisition or use.

Frequently Asked Questions (FAQs)

1. What is the chemical structure of 5-MeO-MiPT?
   It features an indole base substituted with a methoxy group at the 5-position, with methyl and isopropyl groups attached to the amine nitrogen.

2. What are the common research applications of 5-MeO-MiPT?
   It is mainly used to study serotonin receptor binding and psychedelic pharmacology.

3. How pure is research-grade 5-MeO-MiPT?
   Typically, it is supplied at a purity of 98% or higher.

4. What safety precautions should be taken?
   Use gloves, eyewear, and work in a ventilated area to avoid exposure.

5. Is 5-MeO-MiPT legally restricted?
   Legal status varies by country; it is controlled in some jurisdictions and unscheduled in others.

Conclusion

5-MeO-MiPT 10mg pellets are a high-purity synthetic tryptamine derivative used primarily for research purposes within neurochemical and pharmacological fields. Its distinct serotonergic receptor profile and physical stability in pellet form make it a practical compound for controlled scientific studies. Proper laboratory safety and regulatory awareness are essential when handling this material.