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ADB-FUBINACA research chemical properties

CAS: 1445583-51-6
Formula: C21H23FN4O2
Molecular weight: 382.430
Compound purity: > 99.7%
Appearance: Powder

Information about ADB-FUBINACA

ADB-FUBINACA official designation within the IUPAC product is defined N-[(1S)-1-(aminocarbonyl)-2-methylpropyl]-1-[(4-fluorophenyl)methyl]-1H-indazole-3-carboxamide, and straightforward chemical formula from the substance is summarized as, C20H21FN4O2 using the molecular weight going to be 368.4 g/mol. The physiological and toxicological qualities of the compound aren’t known. The product is meant for forensic and research applications.

ADB-FUBINACA seems to be the product of rational drug design because it is different from Abdominal-FUBINACA only through the substitute from the isopropyl group has a tert-butyl group. In 2013, ADB-FUBINACA was identified erectile dysfunction in recreational products by Japanese forensic scientists. In Europe, it was initially reported on 28 November 2013, in Poultry and Germany. ADB-FUBINACA is really a study chemical that functions as a potent agonist for those cannabinoid receptors which first is discovered in 2013 in Japan inside a smoking mixture. The enantiomer of the substance was initially produced by Pfizer in ’09 being an analgesic medication but never went after for human use.

ADB-FUBINACA is generally sprayed on botanical material and smoked or vaporized to attain a fast start of effects and rapid offset. ADB-FUBINACA is orally active when dissolved inside a fat, which could boost the duration considerably. Like other cannabinoids, it’s insoluble in water but dissolves in ethanol and lipids. ADB-FUBINACA binds towards the same brain receptor as THC, the ingredient of marijuana, and it has been proven to create similar medicinal effects.

On-line ADB-FUBINACA is offered like a white-colored powder or very, packaged in an aluminum foil bag. The compound wholesomeness is 99.5%-99.7%. The precise dose isn’t known, but ADB FUBINACA is slightly less potent compared to CHMINACA be substances. It should be in small increments from about .5 mg to at least one-2mg when the effect starts. This describes inhaled consumption. Whether dental consumption (or any other application) can be done, is unknown.

ADB-FUMINACA has the capacity to, dose-dependently, decrease body temperature and heartbeat at doses of 3 mg. One dying through coronary arterial thrombosis continues to be associated with ADB-FUBINACA intoxication. The hypothermic e ects of ADB-FUBINACA seem to become mediated through CB1 receptors and is reversed by pretreatment with CB1 antagonist rimonabant (an anorectic antiobesity drug that’s been withdrawn in the market because of costly negative effects) although not CB2 antagonist SR144528(a medication that functions like a potent and highly selective CB2 receptor inverse agonist).

Unverified sources report: Habitually I mix it in certain juice at 15mg/ml and vape it inside an in. People explained that 3mg eaten could be pretty strong and last forever and it’s better to start around .5mg-1mg without tolerance, so i ingested .05ml of my juice (750ug) including go water. 30 min later I had been feeling it and can turn the high is sensational looking really relaxed, just like a light cannabis edible or perhaps a low dose of benzo. After 1 hrs still that top I made the decision to top it a little but didn’t ˉt added an excessive amount of length to my high and so i made the decision to decrease around 500ug straight within my nose. Wow! The show-up is almost instant and I’ve passed from the nice relaxation to light visuals in five minutes.

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