Fluetizolam Pellets – 1mg

A. Introduction

Fluetizolam Pellets 1mg are premium laboratory-grade research pellets containing thienotriazolodiazepine analog, designed for scientific institutions and analytical laboratories investigating novel psychoactive substance classes. This high-purity compressed pellet format provides researchers with consistent microgram units for trace-level method validation, structural analysis, and reference comparisons in controlled settings.

B. Scientific Overview

Fluetizolam belongs to the thienotriazolodiazepine class structurally analogous to etizolam derivatives, characterized by its fused thiophene-triazole-benzodiazepine scaffold suitable for analytical profiling. In research contexts, it functions as an analytical reference for studying chromatographic behavior, mass spectrometry fragmentation patterns, and spectroscopic signatures of thienodiazepine structures.

Laboratory investigations focus on its chemical properties, including low-dose solubility profiles, thermal stability, and quantitative recovery characteristics under analytical conditions, without reference to biological interactions.

C. Product Specifications

• Form: Compressed microdose pellets containing 1mg Fluetizolam per unit for precise lab handling

• Label per unit: 1mg analytical portions (resealable packaging)

• Synonym: 4-(2-fluorophenyl)-2-ethyl-9-methyl-6H-thieno[3,2-f]triazolo[4,3-a]diazepine

• CAS Number: 40054-88-4

• Molecular Formula: C₁₇H₁₅FN₄S

• Molecular Weight: 326.39 g/mol

• Purity: ≥98% (HPLC, typical batch purity)

• Storage Conditions: -20°C freezer, desiccated, protected from light/moisture for stability

D. Laboratory Use Context

Fluetizolam Pellets 1mg are designated solely for in-vitro analytical research, including trace-level reference standard preparation, LC-MS/MS method optimization at ng/mL concentrations, forensic toxicology screening, and impurity detection in complex biological matrices.

Researchers apply them in controlled environments for ultra-sensitive quantitative analysis, positive ionization studies ([M+H]+), and stability testing via UHPLC-HRMS protocols. The microdose pellet format ensures reproducible low-level mass transfer critical for LOD/LOQ determination.

E. Quality & Testing

Every batch receives comprehensive quality control:

• Certificate of Analysis (COA) with HPLC, LC-MS, NMR identity confirmation and pellet uniformity testing

• Full batch traceability from synthesis through compression and verification

• Third-party laboratory testing for purity, homogeneity, content uniformity (<2% RSD), and residual solvents

• Manufactured under controlled conditions ensuring consistent microdose pellet performance

F. Shipping & Handling

Discreet worldwide shipping to verified research laboratories via secure, temperature-controlled carriers. Specialized low-dose packaging meets IATA/DOT standards for Schedule I research chemicals, with desiccant protection and comprehensive import documentation. Tracking provided; buyers confirm jurisdictional compliance prior to purchase.

G. Compliance Disclaimer

For Research Use Only. Not for human consumption.
This product constitutes a controlled laboratory reagent supplied strictly for analytical research purposes. Not approved for human, veterinary, diagnostic, or therapeutic applications. No statements imply biological activity beyond controlled in-vitro analytical contexts.

Qualified researchers and institutions assume complete responsibility under local, federal, and international regulations. Seller disclaims all liability for non-research applications. Consult safety data sheets and institutional protocols before handling.