Federal Analogue Act

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Federal Analogue Act
House Post Office and Civil Service, House Public Works and Transportation, House Ways and Means
  • Passed the House on 11 September 1986 (392-16)
  • Passed the Senate on 30 September 1986 (97-2, in lieu of S. 2878) with amendment
  • House agreed to Senate amendment on 17 October 1986 (unanimous consent) with further amendment
  • Senate agreed to House amendment on 17 October 1986 (voice vote)
  • Signed into law by President Ronald Reagan
  • on 27 October 1986

    The Federal Analogue Act, 21 U.S.C. § 813, is a section of the United States Controlled Substances Act passed in 1986 which allows any chemical "substantially similar" to a controlled substance listed in Schedule I or II to be treated as if it were listed in Schedule I, but only if intended for human consumption. These similar substances are often called designer drugs. The law's broad reach has been used to successfully prosecute possession of chemicals openly sold as dietary supplements and naturally contained in foods (e.g., the possession of phenethylamine, a compound found in chocolate, has been successfully prosecuted based on its "substantial similarity" to the controlled substance methamphetamine).[1] The law's constitutionality has been questioned by now Supreme Court Justice Neil Gorsuch[2] on the basis of Vagueness doctrine.


    Definition

    21 U.S.C. § 802(32)

    Case law

    United States v. Forbes

    United States v. Forbes, 806 F. Supp. 232 (D. Colo. 1992), a Colorado district court case, considered the question of whether the drug

    (DET).

    AET

    DMT

    DET

    In this case, the court ruled that AET was not substantially similar to DMT or DET, on the grounds that (i) AET is a

    tertiary amines
    , (ii) AET cannot be synthesized from either DMT or DET, and (iii) the hallucinogenic or stimulant effects of AET are not substantially similar to the effects of DMT or DET. Furthermore, the court ruled that the definition of controlled substance analogue given in the Federal Analogue Act was unconstitutionally vague, in that

    "Because the definition of 'analogue' as applied here provides neither fair warning nor effective safeguards against arbitrary enforcement, it is

    void for vagueness."[3]

    The common law principle that the people should have the right to know what the law is, means that the wording of laws should be sufficiently clear and precise that it is possible to give a definitive answer as to whether a particular course of action is legal or illegal. However, despite this ruling the Federal Analogue Act was not revised, and instead AET was specifically scheduled to avoid any future discrepancies.

    As a district court decision, this case is no

    binding precedent
    .

    United States v. Washam

    United States v. Washam (2002) 312 F.3d 926, 930 was an appellate decision for the

    gamma-hydroxybutyrate
    (GHB).

    1,4-B

    GHB

    In this case the court ruled that 1,4-B was substantially similar to GHB, on the grounds that (i) "1,4-Butanediol and GHB are both linear compounds containing four carbons and that there is only one difference between the substances on one side of their molecules", and, more importantly, (ii) that 1,4-B is metabolized into GHB by the body and so produces substantially similar physiological effects.[4]

    It was raised in defense that 1,4-B and GHB contain different functional groups.[citation needed] but these were not held to be grounds to consider 1,4-B not substantially similar to GHB.

    It was also raised in the case of Washam that the Federal Analogue Act was unconstitutionally vague, but in this case the court rejected this argument on the grounds that the defendant's actions in concealing her activities and lying to DEA agents showed that she knew her actions were illegal, and furthermore that "…a person of common intelligence has sufficient notice under the statute that 1,4-Butanediol is a controlled substance analogue." The court in Washam construed the Analogue Act to require parts A(i) and either A(ii) or A(iii), and concluded the Act was constitutionally permissible upon this construction.

    As a result of Washam, the Federal Analogue Act has been upheld (at least for the states and territories comprising the eighth judicial circuit) and can be considered valid at the present time.

    However, a jury in Federal District Court in Chicago in a different case found 1,4-butanediol not to be an analog of GHB under federal law, and the

    Seventh Circuit Court of Appeals upheld that verdict and so 1,4-butanediol is currently not a controlled substance analogue.[5]

    See also

    References

    1. ^ "citing United States v. McKinney, 79 F.3d 105 (8th Cir. 1996)".
    2. ^ Fels, Andrew, Voiding the Federal Analogue Act (February 12, 2021). Nebraska Law Review, Vol. 100, No. 3, 2022, Available at SSRN: https://ssrn.com/abstract=3736304 or http://dx.doi.org/10.2139/ssrn.3736304
    3. ^ "US Federal Analogue Act Found to Require Structural Similarity". erowid. Retrieved 17 May 2013.
    4. ^ "UNITED STATES v. WASHAM". findlaw. Retrieved 17 May 2013.
    5. ^ United States v. Turcotte, 405 F.3d 515 (7th Cir. 2005) "With specific regard to 1,4 Butanediol, the jury has returned a special verdict which states that 1,4-Butanediol is not a Schedule I Narcotic Drug Controlled Substance analogue, because 1,4-Butanediol's chemical structure is not significantly similar to the chemical structure of GHB.

    External links