This product entry features 6-APB Succinate, an aminoalkylbenzofuran derivative offered exclusively as a generic, brandless compound to support independent scientific experimentation. Engineered to meet or exceed a baseline standard of ≥98% purity, this chemical reagent serves as an essential tool for forensic testing, structural elucidation, and receptor affinity mapping. The succinate salt form provides enhanced long-term stability and consistent material properties during handling, preventing premature degradation during routine laboratory measurements.

For research use only. Not for human or veterinary use. Not for clinical, diagnostic, or consumptive applications. This compound is strictly restricted from any biological testing involving live subjects and must be managed within a certified facility.

Chemical Identity & Classification
The systematic documentation of this compound ensures structural transparency for validated research protocols. The core chemical identity is summarized below:

Formal Chemical Name: 1-(1-benzofuran-6-yl)propan-2-amine succinate

CAS Registry Number: 286834-85-3 (Free base base CAS: 286834-85-3 / Hydrochloride variant: 286834-84-2)
Wikipedia

Molecular Formula: C
11
​
H
13
​
NO⋅C
4
​
H
6
​
O
4
​
(representing the 6-APB base complexed with succinic acid)

Molecular Weight: 175.23 g/mol (Free Base) / 293.32 g/mol (Succinate salt form)
Wikipedia

Synonyms: 6-(2-Aminopropyl)benzofuran succinate, alpha-Methyl-6-benzofuranethanamine succinate

Primary Classification: Synthetic benzofuran reagent, phenethylamine structural analog, analytical reference material

Chemical & Physical Characteristics
In its standard isolated state, 6-APB Succinate typically presents as a fine, off-white to light tan crystalline powder or granular solid. The pairing with succinic acid yields a distinct physical matrix compared to standard hydrochloride salts, often exhibiting lower hygroscopicity (resistance to moisture absorption from ambient air). It displays definitive solubility in typical laboratory solvents, demonstrating excellent dissolution properties in dimethyl sulfoxide (DMSO), dimethylformamide (DMF), and methanol, while maintaining moderate solubility in pure water depending on ambient temperature. It possesses a high melting threshold, which serves as a secondary physical metric for assessing sample uniformity.

Purity & Analytical Verification
Quality assurance is maintained through strict analytical thresholds. Every batch of this research chemical is certified at ≥98% purity, minimizing the presence of synthetic precursors, side-reaction isomers, or heavy metal remnants. Verification is achieved utilizing a comprehensive multi-instrumental approach:

High-Performance Liquid Chromatography (HPLC): Used to confirm the absolute purity profile and track peak integration.

Gas Chromatography-Mass Spectrometry (GC-MS) / LC-MS: Employed to verify structural fragmentation patterns and molecular mass consistency.

Nuclear Magnetic Resonance Spectroscopy (NMR): Used to resolve carbon and proton alignment, verifying the exact 6-position isomerism of the aminopropyl chain.

A detailed Certificate of Analysis (COA) detailing these metrics is generated for every production lot and can be provided upon institutional request.

Quality Control & Batch Integrity
To fulfill the requirements of high-level industrial R&D and academic research, this compound undergoes stringently managed batch-controlled manufacturing. Each production run is assigned a unique, trackable lot number that provides full transparency from raw component sourcing to primary packaging. Our quality control tracking guarantees that chemical reagents are shielded from cross-contamination, ensuring that longitudinal studies can rely on absolute reproducibility between distinct orders. No third-party branding is applied, keeping focus entirely on structural integrity and biochemical conformity.

Safety, Handling & Laboratory Precautions
As an uncharacterized novel reagent, 6-APB Succinate must be treated as a potentially hazardous substance with unknown toxicological properties. Laboratory technicians are required to implement full protective protocols upon receipt. At minimum, operations must utilize standard personal protective equipment (PPE), including nitrile laboratory gloves, chemical safety goggles, and appropriate body coverings such as protective lab coats.

All weighing, transfer, and dilution steps should take place inside a validated chemical fume hood or localized negative-pressure environment to avoid accidental particulate inhalation. Before procurement, institutions should consult the comprehensive Material Safety Data Sheet (MSDS/SDS) associated with this chemical class to implement proper spill-containment and emergency neutralization procedures.

Packaging, Labeling & Storage
To protect the material against environmental degradation and moisture-induced decomposition, this chemical reagent is enclosed in professional, laboratory-grade packaging. The inner containment uses thick, anti-static, light-blocking amber glass vials or high-density polymers, safely secured with tamper-evident, airtight seals. Labels are printed in full alignment with international chemical distribution regulations, prominently displaying the chemical identifier, CAS number, batch tracking ID, and explicit laboratory use warnings.

For maximum shelf-life preservation, it is highly recommended to store the sealed container in a cool, dry location, preferably in a laboratory freezer maintained at or below -20°C.

Intended Research Use & Market Positioning
This compound is positioned on the market solely as an analytical standard and reagent for industrial, forensic, and academic sectors. Its specific structural properties make it a subject of active study within chemical taxonomy labs investigating structure-activity relationships (SAR) of the benzofuran ring system, as well as in vitro affinity screening against targeted monoamine transporter proteins. It is not intended for clinical diagnostics, veterinary therapy, agricultural use, or cosmetic development. Procurement requests are audited to ensure distribution is restricted to verifiable research entities.

Ordering, Availability & Fulfillment
Our eCommerce portal features reliable inventory management, ensuring that listed reagents are in stock and ready for immediate deployment to your facility. The secure checkout pipeline utilizes end-to-end data encryption to safeguard your administrative information, satisfying payment processor compliance criteria. Following order validation, shipments are dispatched in discreet, robust external packaging designed to withstand transit friction. All shipments are accompanied by dedicated tracking numbers, enabling your procurement team to monitor delivery timelines precisely.

Legal & Regulatory Disclaimer
For research use only. Not for human or veterinary use. Not for clinical, diagnostic, or consumptive applications. This product is a generic chemical reagent intended exclusively for specialized laboratory research conducted by qualified professionals. The purchasing entity assumes full and unconditional responsibility for verifying the legal status of 6-APB Succinate within their local country, state, or municipal jurisdiction prior to making a purchase. The vendor bears no liability for any unauthorized handling, domestic restrictions, or regulatory enforcement actions arising from improper legal verification.