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In the early 2000s, synthetic cannabinoids were diverted for abuse. Illicit producers are still releasing new chemicals for recreational use even after laws have been passed to prohibit substances currently available on the drug market.

MMB-CHMINACA, ADB-CHMINACA, and other synthetic cannabinoids share structural similarities with the new synthetic cannabinoid Ab-chminaca online for sale. The European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) received the initial identification and report of AB-CHMINACA in 2014, and it continued to receive reports until 2017.  AB-CHMINACA has resurfaced, and laboratories confirmed its detection in April 2024 using standard reference material.

In synthetic cannabinoid GC/MS or LC/MS procedures for urine drug testing, forensic analysis, or clinical toxicology applications, this certified Snap-N-Spike solution can be used as a starting material for controls or calibrators.

Our approved solution standards for synthetic cannabinoids that are currently under federal supervision are DEA-exempt, meaning that labs can make orders for these compounds without having to complete extra regulatory paperwork. There may be state-specific regulatory restrictions for US customers.

Requirements for Handling AB-CHMINACA

The following are some of the requirements for handling AB-CHMINACA. These include the CSA’s schedule I regulatory controls and administrative, civil, and criminal sanctions that apply to the production, distribution, dispensing, import, export, research, and conduct of educational activities:

1. Registration:In accordance with 21 U.S.C. 822, 823, 957, and 958, as well as 21 CFR parts 1301 and 1312, anyone who handles, distributes, imports, exports, conducts research or conducts chemical analysis with, or possesses, ab-chminaca, or who desires to buy ab-chminaca online, must register with the DEA.

2. Security: AB-CHMINACA is subject to schedule I security requirements and must be handled and stored in accordance with 21 CFR 821, 823, 871(b), and 21 CFR 1301.71 through 1301.93.
3. Packaging and Labeling: All labels and labeling for commercial containers of AB-CHMINACA must comply with 21 U.S.C. 825 and 958(e) and 21 CFR part 1302.

4. Quote:

Under 21 U.S.C. 826 and 21 CFR part 1303, only registered manufacturers are allowed to manufacture AB-CHMINACA in accordance with a quota assigned under 21 CFR part 1303.

5. Inventory:

In accordance with 21 CFR 1304.03, 1304.04, and 1304.11 (a) and (d) and 21 U.S.C. 827 and 958, every DEA registrant that has any quantity of AB-CHMINACA on hand as of October 16, 2017, must inventory all stocks of these substances on hand as of that date.

Current DEA registrants have 30 calendar days from the order’s effective date to complete all inventory requirements.

Following the initial inventory, each DEA registrant is required by 21 U.S.C. 827 and 958, as well as 21 CFR 1304.03, 1304.04, and 1304.11, to take a new inventory of all controlled drugs (including AB-CHMINACA and THJ-2201) on hand every two years.

6. Documents and Reports.

According to 21 CFR parts 1304 and 1312, as well as 21 U.S.C. 827 and 958(e), each DEA registrant is required to keep records and submit reports regarding AB-CHMINACA.

7. Order forms.

In accordance with 21 CFR part 1305 and 21 U.S.C. 828, all DEA registrants who distribute AB-CHMINACA are required to maintain compliance with the order form requirements.

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