Bromazolam Powder Sales

Buy Bromazolam Powder Online

Sell Bromazolam Powder Online

Sell Bromazolam Powder Online

Sell Bromazolam Powder Online. USA Warehouse Sell 100 % Pure Bromazolam Powder Cas Number 71368-80-4 At Cheap Price

We are suppliers and manufacturers of bromazolam powder online

BrandBromazolam
Usage/ApplicationMetal
ColorWhite
FinishSemi Glossy
CategoriesRegular Solid Colors

Bromazolam (Chemical Abstracts Service [CAS] registry number: 71368-80-4; CAS name: 8-bromo-1-methyl6-phenyl-4H-S-triazolo[4, 3-a][1, 4]benzodiazepine) is a triazolobenzodiazepine that was originally developed as a candidate medication

Product Specification

BrandBromazolam
Usage/ApplicationMetal
ColorWhite
FinishSemi Glossy
CategoriesRegular Solid Colors
Packaging Size10 Kg
Nearest RAL Codemention at pack
TypeThermoset
Packaging TypeCorrugated Box
Country of OriginMade in India
Minimum Order Quantity1 Kg

Product Description

Bromazolam (Chemical Abstracts Service [CAS] registry number: 71368-80-4; CAS name: 8-bromo-1-methyl6-phenyl-4H-S-triazolo[4,3-a][1,4]benzodiazepine) is a triazolobenzodiazepine that was originally developed as a candidate medication but was never approved for use. The first documented detection of bromazolam by government authorities was in Sweden in 2016. Since then, the compound has been detected in products or in biological samples in nine countries: Australia, Austria, China, Finland, Germany, India, Sweden, the United Kingdom (Wales) and the USA.

Additional Information

Item Code350012
Delivery Time2 to 7 days
Production Capacity50000000
Packaging DetailsBromazolam phase I metabolism is mediated primarily by several isoforms of the CYP450 enzyme system (CYP2B6, CYP2C19, CYP3A4, CYP3A5 and CYP2C9), whereas phase II metabolism involves the isoenzymes UGT1A4 and UGT2810. Monohydroxylated metabolites include 4-hydroxylated bromazolam and -hydroxy bromazolam, with an additional dehydroxylated metabolite, -5-dihydroxy-bromazolam. After glucuronidation, -hydroxy glucuronide and N-glucuronide are the most abundant phase II metabolites. Information on the compound’s pharmacodynamics is confined to a single in-vitro study of its binding to  subunits of the -aminobutyric acid type A/benzodiazepine receptor complex. Bromazolam was nonselective for  subunits, showing measurable binding affinity at receptors containing 1 (Ki = 2.8 nM), 2 (Ki = 0.69 nM) and 5 (Ki = 0.62 nM) subunits.

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