Buy AMT Powder

Product Overview

AMT Powder offers alpha-methyltryptamine (AMT) in a free-flowing solid form tailored to the needs of professional laboratories that require reliable, traceable research chemical inputs. As a synthetic tryptamine derivative, AMT is supplied here as a brandless, non-pharmaceutical compound with a defined purity specification of ≥98%, supporting demanding analytical and experimental environments.

The product is designed exclusively for use in controlled research settings by trained personnel familiar with small-molecule handling, documentation, and institutional compliance requirements. It is not formulated, presented, or marketed for any human or veterinary exposure, and no claims are made regarding clinical, pharmacological, or outcome-based characteristics. For research use only. Not for human or veterinary use. Not for clinical, diagnostic, or consumptive applications.

Chemical Identity & Classification

Alpha-methyltryptamine (AMT) is a synthetic indole-based compound structurally derived from tryptamine, featuring a methyl substitution at the alpha position of the side chain. This modification situates AMT within the substituted tryptamine family, a group of small molecules commonly encountered in advanced analytical, forensic, and reference-standard work.

Key identifiers include:

• Preferred name: Alpha-methyltryptamine (AMT)

• CAS number: 299-26-3

• Molecular formula: C11H14N2

• Molecular weight: 174.24 g/mol (approx.)

• Representative synonyms: α-methyltryptamine; 3-(2-aminopropyl)indole; Indopan; 1-(1H-indol-3-yl)propan-2-amine.

Within a research context, AMT is typically classified as:

• A synthetic tryptamine-class research chemical.

• A small-molecule reference or analytical reagent suitable for use in non-clinical method development and profiling under appropriate controls.

Chemical & Physical Characteristics

In its research-grade form, AMT is described as a solid organic compound, often obtained as a crystalline or microcrystalline powder. Reference data indicate that AMT and its hydrochloride salt can appear as off-white to white crystalline material, with the hydrochloride form reported as a white crystalline powder in technical summaries.

The compound contains an indole ring system attached to a substituted propan-2-amine side chain, influencing its interactions with aqueous and organic media. Tryptamine derivatives such as AMT are generally characterized by limited water solubility and greater solubility in polar organic solvents, though exact solubility parameters depend on the specific salt form and conditions. Typical laboratory considerations for indole-based compounds include potential sensitivity to light, oxidation, and elevated temperatures, making controlled storage and minimal unnecessary exposure important to preserve material integrity.

Physical attributes such as particle size, bulk density, and observed appearance for a given lot are normally detailed on the accompanying certificate of analysis (COA) or technical data sheet. These details allow analytical or formulation teams to account for handling characteristics when designing internal workflows and method protocols.

Purity & Analytical Verification

AMT Powder is specified at a minimum purity of ≥98%, aligning with expectations for high-grade research chemicals and analytical reference materials. This purity specification supports applications where minor impurities, synthesis byproducts, or residual reagents may influence chromatographic separations, spectral signatures, or other analytical outputs.

Verification of identity and purity for AMT typically relies on industry-standard analytical methodologies including high-performance liquid chromatography (HPLC), gas chromatography (GC), nuclear magnetic resonance (NMR) spectroscopy, and mass spectrometry (MS or LC‑MS). These techniques collectively help confirm the molecular structure, assess impurity profiles, and ensure batch-to-batch consistency against defined acceptance criteria. Batch-specific COAs summarizing key results and instrumental methods are usually available to qualified customers on request, supporting internal QA processes and audit requirements.

Quality Control & Batch Integrity

Production of AMT Powder is managed under controlled conditions, with each batch assigned a unique lot identifier to ensure full traceability from synthesis through packaging and distribution. This traceable framework allows laboratories to link physical material with the exact COA, SDS, and any supplementary technical information associated with that lot.

Quality control practices for research chemicals generally encompass confirmation of identity, purity, appearance, and correct labeling, along with verification that packaging and documentation meet applicable internal and regulatory standards. Where appropriate, cross-checks using independent instrumentation or third-party laboratories may be employed to strengthen confidence in reported analytical data. Documented QC procedures and version-controlled analytical methods help support consistent material supply and transparent communication with end users.

Safety, Handling & Laboratory Precautions

AMT Powder is intended solely for use by trained professionals working in suitably equipped laboratory environments under institutional oversight. Standard good laboratory practice should be followed at all times, including the use of appropriate personal protective equipment such as gloves, protective eyewear, and lab coats, and working within adequate ventilation or containment systems as required by internal policies.

Users should consult the substance-specific safety data sheet (SDS/MSDS) for detailed information on hazard classification, potential exposure routes, accidental release measures, and recommended storage and disposal procedures. Laboratories should avoid generating unnecessary dust or aerosols, prevent uncontrolled release of the material, and handle spills or waste in accordance with local regulations and institutional protocols. No advice is provided or implied regarding administration, exposure, or any clinical context, and all handling must remain strictly within non-clinical research frameworks.

Packaging, Labeling & Storage

AMT Powder is supplied in research-grade primary containers designed to protect the solid material during normal handling, storage, and shipping. Containers are typically securely sealed and may incorporate tamper-evident features, allowing end users to confirm that the product has not been opened or altered prior to receipt.

Labels generally include core identifiers such as product name or code, chemical designation, CAS number, lot or batch number, and relevant hazard or precautionary statements consistent with applicable regulations. Typical storage recommendations for AMT and related tryptamine derivatives include keeping the container tightly closed in a cool, dry place, protected from light and sources of heat, to help maintain long-term stability. Final storage conditions and any additional requirements are specified in the SDS and COA, which laboratories should consult when defining internal storage and access controls.

Intended Research Use & Market Positioning

AMT Powder is positioned strictly as a research chemical for use by qualified laboratories operating within appropriate legal and institutional frameworks. Potential application areas include analytical chemistry, method development, forensic or toxicological reference work, and comparative studies involving substituted tryptamine structures where such activities are permitted.

The product is not manufactured, advertised, or supplied for human or veterinary use, nor is it intended for clinical, diagnostic, or consumptive applications, and no performance, outcome, or effect-related claims are associated with it. End users are expected to possess the necessary technical expertise and approvals to handle controlled or scheduled materials, should such designations apply in their jurisdiction.

Ordering, Availability & Fulfillment

AMT Powder is made available for purchase to verified research customers through secure ordering channels suitable for institutional and professional procurement. Order confirmations typically include clear product identifiers, CAS number, and lot information to facilitate accurate internal logging and inventory management.

Availability may be influenced by stock levels, regulatory controls, and regional restrictions associated with alpha-methyltryptamine and related tryptamine-class materials. Shipments are generally prepared in robust, discreet packaging with tracked delivery options where available, supporting secure transit and documented receipt at laboratory facilities. Support teams can assist with documentation requests such as COAs and SDS files and can address pre‑purchase questions within the constraints of non-clinical research guidance and regulatory compliance.

Legal & Regulatory Disclaimer

This product is supplied strictly as a research chemical for use in laboratory settings by qualified professionals operating under appropriate institutional and regulatory oversight. It is not approved, marketed, or suitable for human or veterinary use, and must not be employed for clinical, diagnostic, therapeutic, or consumptive purposes under any circumstances.

All responsibility for compliance with applicable local, national, and international regulations—including any scheduling, licensing, import/export, or handling restrictions relevant to alpha-methyltryptamine—rests solely with the purchaser and end user. For research use only. Not for human or veterinary use. Not for clinical, diagnostic, or consumptive applications.