MEMORANDUM OPINION
ELLIS, District Judge.
At issue in this matter is whether the three defendants violated 21 U.S.C. § 846, Conspiracy to Possess and Distribute a Controlled Substance Analogue, when they represented to a purchaser that the pills they were selling him contained 3,4-me-thylenedioxymethamphetamine (MDMA), a federally-controlled substance, when in fact the pills contained nothing more than ginseng and vitamin B. More specifically, the question presented is whether pills containing ginseng and vitamin B, when represented to contain a schedule I controlled substance, constitute a “controlled
substance analogue” under 21 U.S.C. § 802(32)(A).
I.
The three defendants in this matter, Lloyd T. Clifford, Donald Dwayne Sell-man, and Daniel Edward Johnson devised a scheme in which they would buy quantities of pills containing ginseng and vitamin B, repackage the pills, and then sell them at a handsome profit by representing them to be MDMA, commonly known as “ecsta-cy,” “XTC,” or simply “E.” Pursuant to this scheme, Clifford advised a potential MDMA customer, who as it turned out, was a confidential informant (the “Cl”) that he could sell the Cl a quantity of MDMA pills. The Cl agreed to buy 500 MDMA tablets from Clifford and the transaction occurred the next day, with Clifford and Johnson delivering to the Cl 500 pills they represented to contain MDMA in return for $5,250. In fact, the pills contained no MDMA, but were only over-the-counter ginseng tablets. At the time of this initial transaction, Clifford and Johnson also informed the Cl that they could provide him with 5,000 additional MDMA pills at $5 to $6 per pill and that they could fulfill the Cl’s future requests for MDMA. In fact, defendants never intended to supply the Cl with anything other than over-the-counter pills, which defendants knew did not have the stimulant, depressive, or hallucinogenic effects on the central nervous system that are the hallmark of listed controlled substances.
Consistent with their intention, defendants consummated a second transaction with the Cl a few weeks later. On this occasion, defendants sold the Cl 1,000 pills they represented were MDMA, but in fact contained only vitamin B. The sale price was $9.25 per pill. Defendants were arrested shortly thereafter and subsequently indicted on three charges:
(i) conspiracy to possess and distribute a controlled substance analogue, in violation of 21 U.S.C. § 846;
(ii) conspiracy to steal money and other property of the United States, in violation of 18 U.S.C. § 871; and
(in) forfeiture of drug-related assets, pursuant to 21 U.S.C. § 853.
The three defendants pled guilty
to conspiracy to possess and distribute a controlled substance analogue, in violation of Count I of the three count indictment. Pursuant to the terms of the plea agreement, Counts II and III were dismissed. Clifford and Sellman were scheduled to be sentenced on March 29, 2002, whereas Johnson was scheduled to be sentenced on April 12, 2002.
At the sentencing hearing for Clifford and Sellman on March 29, the Court
sua sponte
raised the question whether the sale of ginseng and vitamin B, represented to be MDMA, was covered by 21 U.S.C. § 802(32)(A). The parties were directed to submit supplemental memoranda on this question and whether an order should issue (i) vacating the order dismissing Counts II and III of the indictment, (ii) vacating defendants’ plea of guilty to Count I of the indictment, (iii) dismissing Counts I and III of the indictment, and (iv) ordering the prosecution to proceed only as to Count II of the indictment. Following two hearings, the Court ruled that defendants’ conduct was not covered by the controlled substance analogue statute and hence the Court (i) vacated the Janu
ary 28, 2002 order dismissing Counts II and III of the indictment, (ii) vacated defendants’ pleas of guilty to Count I of the indictment, (iii) dismissed Count I, and, accordingly, Count III of the indictment, and (iv) ordered the prosecution to proceed to trial as to Count II of the indictment. This memorandum opinion sets forth the reasons for this ruling.
II.
The central question presented is whether ginseng or vitamin B, misrepresented to be MDMA, fits within the statutory definition of a “controlled substance analogue” in 21 U.S.C. § 802(32)(A). If so, then, in accordance with their pleas, defendants may be found guilty of conspiracy to possess and distribute a controlled substance analogue, in violation of 21 U.S.C. § 846, and their pleas were valid. But if not, then defendants’ conspiracy to sell ginseng and vitamin B pills to the Cl, representing those pills to contain MDMA, might violate some federal criminal law, but it would not violate Section 846.
Passed as part of the Anti-Drug Abuse Act of 1986, 99 P.L. 570; 100 Stat. 3207 (1986), the Controlled Substance Analogue Enforcement Act of 1986 provides that
the term “controlled substance analogue” means a substance-
(i) the chemical structure of which is substantially similar to the chemical structure of a controlled substance in schedule I or II;
(ii) which has a stimulant, depressant, or hallucinogenic effect on the central nervous system that is substantially similar to or greater than the stimulant, depressant, or hallucinogenic effect on the central nervous system of a controlled substance in schedule I or II; or
(iii) with respect to a particular person, which such person represents or intends to have a stimulant, depressant, or hallucinogenic effect on the central nervous system that is substantially similar to or greater than the stimulant, depressant, or hallucinogenic effect on the central nervous system of a controlled substance in schedule I or II.
21 U.S.C. § 802(32)(A). Whether the ginseng and vitamin B pills sold by defendants are a controlled substance analogue under Section 802(32)(A) presents a question of statutory construction. More particularly, the question is whether the statute requires subsection (i) to be read in the conjunctive or the disjunctive with respect to subsections (ii) and (iii).
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MEMORANDUM OPINION
ELLIS, District Judge.
At issue in this matter is whether the three defendants violated 21 U.S.C. § 846, Conspiracy to Possess and Distribute a Controlled Substance Analogue, when they represented to a purchaser that the pills they were selling him contained 3,4-me-thylenedioxymethamphetamine (MDMA), a federally-controlled substance, when in fact the pills contained nothing more than ginseng and vitamin B. More specifically, the question presented is whether pills containing ginseng and vitamin B, when represented to contain a schedule I controlled substance, constitute a “controlled
substance analogue” under 21 U.S.C. § 802(32)(A).
I.
The three defendants in this matter, Lloyd T. Clifford, Donald Dwayne Sell-man, and Daniel Edward Johnson devised a scheme in which they would buy quantities of pills containing ginseng and vitamin B, repackage the pills, and then sell them at a handsome profit by representing them to be MDMA, commonly known as “ecsta-cy,” “XTC,” or simply “E.” Pursuant to this scheme, Clifford advised a potential MDMA customer, who as it turned out, was a confidential informant (the “Cl”) that he could sell the Cl a quantity of MDMA pills. The Cl agreed to buy 500 MDMA tablets from Clifford and the transaction occurred the next day, with Clifford and Johnson delivering to the Cl 500 pills they represented to contain MDMA in return for $5,250. In fact, the pills contained no MDMA, but were only over-the-counter ginseng tablets. At the time of this initial transaction, Clifford and Johnson also informed the Cl that they could provide him with 5,000 additional MDMA pills at $5 to $6 per pill and that they could fulfill the Cl’s future requests for MDMA. In fact, defendants never intended to supply the Cl with anything other than over-the-counter pills, which defendants knew did not have the stimulant, depressive, or hallucinogenic effects on the central nervous system that are the hallmark of listed controlled substances.
Consistent with their intention, defendants consummated a second transaction with the Cl a few weeks later. On this occasion, defendants sold the Cl 1,000 pills they represented were MDMA, but in fact contained only vitamin B. The sale price was $9.25 per pill. Defendants were arrested shortly thereafter and subsequently indicted on three charges:
(i) conspiracy to possess and distribute a controlled substance analogue, in violation of 21 U.S.C. § 846;
(ii) conspiracy to steal money and other property of the United States, in violation of 18 U.S.C. § 871; and
(in) forfeiture of drug-related assets, pursuant to 21 U.S.C. § 853.
The three defendants pled guilty
to conspiracy to possess and distribute a controlled substance analogue, in violation of Count I of the three count indictment. Pursuant to the terms of the plea agreement, Counts II and III were dismissed. Clifford and Sellman were scheduled to be sentenced on March 29, 2002, whereas Johnson was scheduled to be sentenced on April 12, 2002.
At the sentencing hearing for Clifford and Sellman on March 29, the Court
sua sponte
raised the question whether the sale of ginseng and vitamin B, represented to be MDMA, was covered by 21 U.S.C. § 802(32)(A). The parties were directed to submit supplemental memoranda on this question and whether an order should issue (i) vacating the order dismissing Counts II and III of the indictment, (ii) vacating defendants’ plea of guilty to Count I of the indictment, (iii) dismissing Counts I and III of the indictment, and (iv) ordering the prosecution to proceed only as to Count II of the indictment. Following two hearings, the Court ruled that defendants’ conduct was not covered by the controlled substance analogue statute and hence the Court (i) vacated the Janu
ary 28, 2002 order dismissing Counts II and III of the indictment, (ii) vacated defendants’ pleas of guilty to Count I of the indictment, (iii) dismissed Count I, and, accordingly, Count III of the indictment, and (iv) ordered the prosecution to proceed to trial as to Count II of the indictment. This memorandum opinion sets forth the reasons for this ruling.
II.
The central question presented is whether ginseng or vitamin B, misrepresented to be MDMA, fits within the statutory definition of a “controlled substance analogue” in 21 U.S.C. § 802(32)(A). If so, then, in accordance with their pleas, defendants may be found guilty of conspiracy to possess and distribute a controlled substance analogue, in violation of 21 U.S.C. § 846, and their pleas were valid. But if not, then defendants’ conspiracy to sell ginseng and vitamin B pills to the Cl, representing those pills to contain MDMA, might violate some federal criminal law, but it would not violate Section 846.
Passed as part of the Anti-Drug Abuse Act of 1986, 99 P.L. 570; 100 Stat. 3207 (1986), the Controlled Substance Analogue Enforcement Act of 1986 provides that
the term “controlled substance analogue” means a substance-
(i) the chemical structure of which is substantially similar to the chemical structure of a controlled substance in schedule I or II;
(ii) which has a stimulant, depressant, or hallucinogenic effect on the central nervous system that is substantially similar to or greater than the stimulant, depressant, or hallucinogenic effect on the central nervous system of a controlled substance in schedule I or II; or
(iii) with respect to a particular person, which such person represents or intends to have a stimulant, depressant, or hallucinogenic effect on the central nervous system that is substantially similar to or greater than the stimulant, depressant, or hallucinogenic effect on the central nervous system of a controlled substance in schedule I or II.
21 U.S.C. § 802(32)(A). Whether the ginseng and vitamin B pills sold by defendants are a controlled substance analogue under Section 802(32)(A) presents a question of statutory construction. More particularly, the question is whether the statute requires subsection (i) to be read in the conjunctive or the disjunctive with respect to subsections (ii) and (iii). Put another way, to establish that a substance is a controlled substance analogue, is it necessary to show subsection (i)
and then
either subsection (ii) or subsection (iii), as defendants argue (hereinafter the “conjunctive interpretation”), or is it sufficient to establish any one of the subsections alone, as the government contends (hereinafter the “disjunctive interpretation”)? Here, it is undisputed that defendants represented that the pills they sold were MDMA, thus clearly satisfying subsection (iii). Thus, if the disjunctive interpretation of Section 802(32)(A) governs, defendants plainly conspired to possess and distribute a controlled substance analogue. Yet, if the conjunctive interpretation applies, then defendants could not have conspired to possess and distribute a controlled substance analogue because ginseng and vitamin B clearly lack a chemical structure similar to MDMA or any other schedule I or II controlled substance. Thus, defendants’ guilt or innocence with respect to Counts I and III of the indictment turns on the statutory interpretation of 21 U.S.C. § 802(32)(A).
Although this statutory interpretation question has not been resolved in this circuit, it is not entirely novel; at least three district courts have had occasion to engage
this issue. Two have determined that the conjunctive interpretation is appropriate,
while another has opted for the disjunctive interpretation.
In these circumstances-the absence of either controlling authority or persuasive uniform authority-the task of statutory interpretation must be undertaken anew.
When interpreting a statute, it is well-established that “[a]ny analysis... must begin with the plain meaning of the statute itself.”
Chris v. Tenet,
221 F.3d 648, 651-52 (4th Cir.2000). Of course, it is improper to confíne the interpretation of a statute to the one section or sections to be construed;
rather, it is appropriate to interpret the Controlled Substance Analogue Enforcement Act as a whole.
And, only if a statute’s plain meaning is ambiguous is it proper to consider the statute’s structure and purpose so as to ascertain Congress’s intent.
See United States v. Jackson,
759 F.2d 342, 344 (4th Cir.1985);
Johnson v. Garraghty,
57 F.Supp.2d 321, 326 (E.D.Va.1999). Thus, the analysis here must begin with the question whether the statute has a plain and unambiguous meaning or is instead infected with an ambiguity.
To be sure, it can be argued, as the district court concluded in
United States v. Greig,
144 F.Supp.2d 386, 389 (D.Vi.2001), that because “[e]ach of the three subordinate clauses occupies the same structural position of subordination relative to the main clause, and each is separated by a semicolon, with the last two clauses being separated by the disjunctive ‘or’,” the series is intended to be read disjunctively.
Id.
Although this point is not without force,
it is neither conclusive, nor ultimately convincing. This is so because there is in fact no universally recognized or authoritatively stated rule of structure to the effect that a series of subordinate clauses must be read in the disjunctive if the penultimate and final clauses are separated by “or.”
While some or even many may invariably follow such a convention, it is clear that Congress is not in this group. Indeed, elsewhere in the very same statute, specifically Section 802(9), Congress elected to follow a contrary convention. There, Congress listed a number of subor
dinate clauses in a fashion similar to Section 802(32)(A), but placed the term “or” after every subsection to denote a clear disjunctive intent.
See
21 U.S.C. § 802(9).
Given the well-established principle of statutory construction that no part of a statute should be rendered inoperative or superfluous,
it follows that Congress apparently felt it necessary, at least in that instance, to place “or” between each subordinate clause to require or ensure a disjunctive reading. So it is clear, therefore, that Congress itself does not invariably follow the convention advocated in
Greig,
nor is there any certain means of determining when it intends to do so and when it does not. Thus, the mere existence of “or” between the last two subordinate clauses cannot be taken to be conclusive evidence that Congress intended all the subordinate clauses to be read in the disjunctive.
And, this point alone suggests that there is an ambiguity in whether the subordinate clauses should be accorded the disjunctive interpretation or the conjunctive interpretation.
But the problematical status of this convention is not the only reason pointing to the statute’s ambiguity; an additional, more compelling reason is that the word “analogue,” which Congress chose to include in Section 802(32)(A) as demarcating the statute’s scope, has a settled meaning that is consistent with the conjunctive interpretation, but flatly inconsistent with the disjunctive interpretation. An analogue, defined in the chemical context, is a “structural derivative of a parent compound that often differs from it by a single element.”
This definition fits well within subsection (i), but not within either subsections (ii) or (iii). Accordingly, only a conjunctive interpretation of the subsections {(i) and [ (ii) or (iii) ]} is faithful to the plain meaning of analogue. This point, if not conclusive in favor of the conjunctive interpretation, is surely compelling evidence of the statute’s ambiguity in this regard.
Given this ambiguity, the interpretive task appropriately expands to include consideration of the statute’s purpose, as reflected in its language and structure as a whole and in its legislative history.
See Jackson,
759 F.2d at 344;
Johnson,
57 F.Supp.2d at 326. In this regard, the evidence favoring a conjunctive interpretation of the subsections is compelling. As noted, in choosing to use the term “analogue” to define the statute’s scope, Congress made clear its intention to limit that scope to substances with structures chemically similar to controlled substances.
Equally compelling is the statute’s legislative history. There is not a scintilla of evidence in the legislative history that Congress intended to cover and criminal
ize sales of legal substances such as flour, salt, ginseng, vitamin B, etc., merely because the seller represents they will yield a stimulant, depressant, or hallucinogenic effect like that of a controlled substance. Nowhere in the legislative history is there any mention or even a suggestion of such a prospect. Instead, the available legislative history indicates unequivocally that the Controlled Substances Analogue Act was, from its inception, designed to combat the problem of persons who seek to avoid the reach of federal criminal drug laws by manufacturing or distributing substances that are not listed controlled substances but which are specifically designed to provide effects that are substantially similar to the effects of listed substances. As the district court in
Forbes
rightly observed, “[t]he [controlled substance] analogue statute is directed at underground chemists who tinker with the molecular structure of controlled substances to create new drugs that are not scheduled.” 806 F.Supp. at 235. Indeed, the Senate’s version of the bill was aimed to confront the “truly frightening problem”
of “persons who specifically set out to manufacture or to distribute drugs which are substantially similar to the most dangerous controlled substances....”
Like its counterpart in the Senate, the House bill focused on underground chemists who sought to evade drug laws by slightly altering controlled substances.
Thus, it is clear that only the conjunctive interpretation effectuates the clear purpose of the statute, namely to criminalize the manufacture and distribution of unlisted substances that are chemically related to listed substances and either have similar effects or are represented to have similar effects. There is simply no indication in the legislative history that the Controlled Substances Analogue Enforcement Act was meant to forbid individuals from passing off over-the-counter nutritional supplements or vitamins as controlled substances.
The government presents two flawed arguments in support of the proposition that the legislative history supports its position. Noting that weeks before the act passed, the three subsections were numbered (i), (ii)(I), (ii)(II) and that the term “and” was written after subsection (i), the government argues that the subsequent omission of the word “and” and the renumbering of the subsections indicates Congress’s clear intent to require the disjunctive interpretation. Yet, there is no evidence establishing the reason for this change. Indeed, it is just as likely that the change was inad
vertent as that it was deliberate. Had the change been deliberate, it would have effected a quite radical alteration in the statute’s scope, criminalizing not just designer drug trafficking, but also distribution of all manner of lawful substances merely because they are represented to be listed substances. Such a radical alteration would surely have occasioned some comment or remark from Congress. The silence in this regard speaks loudly in favor of inadvertence as the explanation for the change.
The government also raised at oral argument that the name of the statute was changed was from the “Designer Drug Enforcement Act” to the “Controlled Substance Analogue Enforcement Act” to signify that the scope of the statute was expanded to include defendants’ situation. The legislative history disagrees. Rather “[t]he name ‘analogue’ was substituted for ‘designer drugs’, because such a name is ‘too appealing a name for these killers.’ ” 131 Cong. Rec. S13,167-02 (daily ed. Oct. 10, 1985) (statement of Senator D’Amato).
Although not directly in point, the Fourth Circuit’s decision in
United States v. Sampson,
140 F.3d 585 (4th Cir.1998) is instructive. There, the court held that “flex,” a mixture of flour, wax, and baking soda, although sold as cocaine, was not a “counterfeit substance,” as defined in 21 U.S.C. § 802(7). In reaching this result, Judge Motz observed that
[sjelling flex does not constitute a crime
punishable by any known federal law.
Simply because a substance looks like cocaine, and the defendant misrepresents to his unsuspecting purchaser that the substance is cocaine, does not make the mere distribution of that substance a violation of the federal narcotics laws.
Id.
at 589 (emphasis added). By the same token, passing off ginseng and vitamin B as MDMA is not “punishable by any known federal law.”
Id.
To be sure, as the government argues, this statement was made in the context of Section 802(7), which defines counterfeit substances, not Section 802(32)(A), which defines controlled substance analogues, and is therefore arguably
dictum.
Yet, there is no reason to believe that Judge Motz and the panel were unaware of Section 802(32)(A) when they made this remark.
Finally, it must be noted that the rule of lenity has no role to play in the interpretative task of the statute. This follows from this circuit’s rule that for the rule of lenity to operate, “there must be a grievous ambiguity or uncertainty in the language and structure of the Act, such that even after a court has seized everything from which aid can be derived, it is still left with an ambiguous statute.”
United States v. Photogrammetric Data Services, Inc.,
259 F.3d 229, 249 (4th Cir.2001) (internal citations and quotation marks omitted). Here, after considering the statute’s language, structure, and purpose, it is clear that Congress intended Section 802(32)(A) to be read con-junctively.
For these reasons, defendants’ pleas of guilty to Count I of the indictment were vacated and Counts I and III of the indictment dismissed.