{"id":1086,"date":"2026-06-16T09:44:45","date_gmt":"2026-06-16T09:44:45","guid":{"rendered":"https:\/\/online-store-108e06d.ingress-erytho.ewp.live\/?post_type=product&p=1086"},"modified":"2026-07-05T22:58:40","modified_gmt":"2026-07-05T22:58:40","slug":"alprazefone-alprazolam-triazolbenzophenone-analogue-2","status":"publish","type":"product","link":"https:\/\/online-store-108e06d.ingress-erytho.ewp.live\/?product=alprazefone-alprazolam-triazolbenzophenone-analogue-2","title":{"rendered":"Alprazefone 4mg\/mL (Alprazolam prodrug) Incoming Next Week (Wedensday)"},"content":{"rendered":"

WARNING!<\/strong><\/u> Category No. 3 substances are <\/strong>NOT<\/strong><\/u> for human consumption OR for veterinary us<\/strong>e!<\/h1>\n

Alprazefone (Alprazolam Triazolobenzophenone analog);<\/strong><\/u> <\/strong>is an analytical reference standard (ARS) categorized as a <\/strong><\/em>non-benzo<\/strong> Benzodiazepine<\/u><\/strong> Derivative<\/u><\/strong>. This product is intended for research studies and may be used as a requirement in some forensic applications. Alprazefone<\/strong><\/u> was part of set of non-benzo benzodiazepine derivatives that were synthesized initially to be soluble in water among other advantages. Once the triazolobenzophenone is introduced into the bloodstream becomes Alprazolam<\/strong><\/u> via central routes through the liver hepatic system.<\/p>\n

Alprazefone’s<\/u><\/strong> prodrug design allows for evaluation of metabolite activation pathways and comparative pharmacological behavior from benzodiazepine<\/u><\/strong>–class<\/strong> compounds. Alprazefone<\/u><\/strong> is of particular interest in analytical, metabolic, and forensic research, where it may be studied for its role in biotransformation pathways, detection profiles, and comparative structural analysis. Its chemical framework supports evaluation through established laboratory techniques, including <\/strong>GC-MS, LC-MS,<\/strong><\/u> and<\/strong> NMR <\/strong><\/u>spectroscopy<\/strong> making it relevant for reference library development and compound identification.<\/p>\n

Alprazefone<\/u><\/strong> is a water-soluble benzodiazepine prodrug that is metabolized in vivo into active triazolobenzodiazepine derivatives (soecifically: Alprazolam), which acts as a supportive ligand at the GABA_A<\/u><\/strong> benzodiazepine receptor complex.<\/p>\n

This material is supplied as a 4mg\/mL solution in propylene glycol (PG) or a sterile water solution in a plastic 20ml container, and is intended exclusively for laboratory<\/strong><\/u> <\/strong>research<\/strong><\/u>, analytical<\/strong><\/u>, & forensic<\/strong><\/u> <\/strong>reference<\/strong><\/u> purposes.<\/p>\n

Alprazefone<\/strong><\/u> is a category 3 <\/strong>New<\/strong><\/u> <\/strong>Psychoactive<\/strong><\/u> <\/strong>Substance<\/strong><\/u>. Alprazefone<\/strong><\/u> may be unsafe to handle. Please be careful when opening packages containing Alprazefone<\/u><\/strong>.<\/p>\n

Safety Data:<\/u><\/strong><\/h1>\n

This material should be considered hazardous until further information becomes available. Do not ingest, inhale, get in eyes, on skin, or on clothing. Wash thoroughly after handling.<\/p>\n

Although limited published research exists on Alprazefone<\/strong><\/u> <\/strong>itself, its chemical framework and substitution pattern allow for evaluation through comparative structural, analytical, and forensic study.<\/p>\n

Understanding the chemical characteristics, spectral behavior, and analytical signatures of Alprazefone<\/u><\/strong> is relevant for laboratory research, forensic comparison, and reference library development. This compound has no approved medical, pharmaceutical, or veterinary applications and has not been evaluated for safety or efficacy in humans or animals.<\/p>\n

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