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| Purity:: | 99.9% | Formula: | C15H20CINO3 |
|---|---|---|---|
| Other Names: | Mmbc | Appearance: | Powder |
| Color: | White | CAS Number: | 24622-60-4 |
MDMB Chminaca Anabolic Steroid Research Chemicals Cannabinoids High Purity
| Product name | mmb-chminaca |
| CAS |
mdmb-chminaca |
| Formula | |
| IUPAC name | (S)-N-(1-Amino-3-methyl-1-oxobutan-2-yl)-1-(4-fluorobenzyl)-1H-indazole-3-carboxamide |
| Molecular weight | 368.40474 |
| Compound purity | 99% |
| Appearance | powder |
| Application | For lab research |
| Storage | Keep in cool and dry place |
| Package | aluminium alloy bag or according to requirement |
| Place of origin | Hongkong |
| Type of shipping | EMS, TNT, FEDEX, DHL, UPS |
| Payment terms | T/T or Western Union or Money Gram or Bitcoin |
| Delivery time | Within 1-3 days |
| MOQ | 10g |
| Production capacity | 500kg/month |
Legal status
Legal status
CA: Schedule II
DE: Anlage II (Prohibited)
Illegal in Austria, China, Croatia, Denmark, Estonia, Finland, Greece, Hungary, Latvia, Lithuania, Louisiana, Luxembourg, Norway, Poland, Turkey, Sweden & Switzerland[1]
Identifiers
CAS Number 1863065-84-2
ChemSpider 34450863
Chemical and physical data
Formula C23H32N2O3
Molar mass 384.52 g·mol−1
MDMB-CHMICA also incorrectly known as MMB-CHMINACA is an indole-based synthetic cannabinoid that is a potent agonist of the CB receptor and has been sold online as a designer drug.
While MDMB-CHMICA was initially sold under the name "MMB-CHMINACA", the compound corresponding to this code name (i.e. the isopropyl instead of t-butyl analogue of MDMB-CHMINACA) has been identified on the designer drug market in 2015 as AMB-CHMINACA.
Over 3600 MDMB-CHMICA seizures between 2014 and 2016 in 19 member states of the European Union have been reported to the European Monitoring Centre for Drugs and Drug Addiction (EMCDDA),[1] including a 40 kg seizure [sic] in Luxembourg in December 2014.
Chemistry.
Several commercial samples of MDMB-CHMICA were found to exclusively contain the (S)-enantiomer based on vibrational and electronic circular dichroism spectroscopy and X-ray crystallography.[7] An (S)-configuration for the tert-leucinate group is unsurprising since MDMB-CHMICA is likely synthesized from the abundant and inexpensive "L" form of the appropriate tert-leucinate reactant.
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