Buy Etizolam (Etilaam/Etizest) Powder Online / Best Price Etizest Powder Online

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Etizolam (Etilaam, Etizest) is a thienodiazepine derivative which is a benzodiazepine analog.The etizolam molecule differs from a benzodiazepine in that the benzene ring has been replaced by a thiophene ring and triazole ring has been fused, making the drug a thienotriazolodiazepine.It possesses amnesicanxiolytic, anticonvulsant, hypnoticsedative and skeletal muscle relaxant properties.

Description

Etizolam (Etilaam/Etizest) is a thienodiazepine derivative which is a benzodiazepine analog.The etizolam molecule differs from a benzodiazepine in that the benzene ring has been replaced by a thiophene ring and triazole ring has been fused, making the drug a thienotriazolodiazepine. Etizolam (Etilaam/Etizest) possesses amnesicanxiolyticanticonvulsanthypnoticsedative and skeletal muscle relaxant properties.
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Etizolam (Etilaam/Etizest) Synonyms:4-(2-chlorophenyl)-2-ethyl-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine;AHR 3219;Y-7131
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Product Overview:
Etizolam (Etilaam/Etizest) is a psychoactive benzodiazepine analog that reportedly has been abused; acts as a full agonist of benzodiazepine receptors Etizolam is a psychoactive benzodiazepine analog with certain medical applications that reportedly has been abused. It acts as a full agonist of benzodiazepine receptors. This product is intended for forensic and research applications. This product is a qualified Reference Material (RM) that has been manufactured and tested to meet ISO17025 and Guide 34 guidelines. These materials are tested using validated analytical methods on qualified instrumentation to ensure traceability of measurements. All traceable RMs may be distinguished by their CofAs and can be downloaded below using the batch number located on the product label. For a representative CofA please contact our technical support.
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Etizolam (Etilaam/Etizest)  Online Public health advisories:
The US Food and Drug Administration (FDA) has issued public health advisories related to this product. Among these, in July 2005, the FDA issued a Public Health Advisory,which advised that “deaths and overdoses have occurred in patients using both the brand name and the generic product.” In December 2007, as part of this continuing investigation, the FDA issued a second Public Health Advisory stating, “The FDA has continued to receive reports of deaths and life-threatening side effects in patients who use this product patch. The reports indicate that doctors have inappropriately prescribed this product patch.In addition, the reports indicate that patients are continuing to incorrectly use this product patch.

Additional information

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