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ADB-BUTINACA
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Buy ADB-BUTINACA Online

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ADB-BUTINACA is a potent agonist of the CB1 and CB2 receptors and is also a potent indole-based cannabinoid. This research chemical is structurally similar to other popular synthetic cannabinoids such as MDMB-BUTINACA. Anecdotal reports have recorded that participants had exhibited effects of euphoria, relaxation and mood enhancement. We offer adbb (adb-butinaca) for sale online

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Description

Buy adbb (adb-butinaca) online
ADB-BUTINACA is a potent agonist of the CB1 and CB2 receptors and is also a potent indole-based cannabinoid. This research chemical is structurally similar to other popular synthetic cannabinoids such as MDMB-BUTINACA. Anecdotal reports have recorded that participants had exhibited effects of euphoria, relaxation and mood enhancement. We offer adbb (adb-butinaca) for sale online

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Disclaimer: Our products are NOT designed for human consumption but research purposes ONLY. Adequate safety precautions should be taken when researching these chemicals. Contact us in other to buy adbb chemical.

ADB-FUBINACA is a designer drug identified in synthetic cannabis blends in Japan in 2013. In 2018, it was the third-most common synthetic cannabinoid identified in drugs seized by the Drug Enforcement Administration.

The (S)-enantiomer of ADB-FUBINACA is described in a 2009 Pfizer patent[3] and has been reported to be a potent agonist of the CB1 receptor and the CB2 receptor with EC50 values of 1.2 nM and 3.5 nM, respectively.[3][4] ADB-FUBINACA features a carboxamide group at the 3-indazole position, like SDB-001 and STS-135. ADB-FUBINACA appears to be the product of rational drug design, since it differs from AB-FUBINACA only by the replacement of the isopropyl group with a tert-butyl group.

Side effects
One death through coronary arterial thrombosis has been linked to ADB-FUBINACA intoxication.

At least an additional 8 deaths in Hungary in 2015 are linked to the usage of this material, all deaths were youngsters below 21.

Metabolism
Twenty-three ADB-FUBINACA major metabolites were identified in several incubations with cryopreserved human hepatocytes. Major metabolic pathways were alkyl and indazole hydroxylation, terminal amide hydrolysis, subsequent glucuronide conjugations, and dehydrogenation.

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Technical Information

Formal Name
N-[(1S)-1-(aminocarbonyl)-2,2-dimethylpropyl]-1-butyl-1H-indazole-3-carboxamide
CAS Number
2682867-55-4
Molecular Formula
C18H26N4O2
Formula Weight
330.4
Purity
≥98%
Formulation(Request formulation change)
A crystalline solid
Solubility
  • DMF: 20 mg/ml
  • DMSO: 5 mg/ml
  • Ethanol: 20 mg/ml
λmax
303 nm
SMILES
O=C(N[C@H](C(N)=O)C(C)(C)C)C1=NN(CCCC)C2=C1C=CC=C2
InChi Code
InChI=1S/C18H26N4O2/c1-5-6-11-22-13-10-8-7-9-12(13)14(21-22)17(24)20-15(16(19)23)18(2,3)4/h7-10,15H,5-6,11H2,1-4H3,(H2,19,23)(H,20,24)/t15-/m1/s1
InChi Key
GPWADXHYJAZPAX-OAHLLOKOSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
Stability
≥ 2 years
Additional information
Weights

100grams, 10grams, 25grams, 500grams, 50grams

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