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Section 5.5 - Recognized controlled substance analogs.

UT Code § 58-37-5.5 (2019) (N/A)
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(1) A substance listed under Subsection (2) is an analog, as defined in Subsection 58-37-2(1)(g), if the substance, in any quantity, and in any material, compound, mixture, or preparation, is present in: (a) any product manufactured, distributed, or possessed for the purpose of human consumption; or (b) any product, the use or administration of which results in human consumption.

(a) any product manufactured, distributed, or possessed for the purpose of human consumption; or

(b) any product, the use or administration of which results in human consumption.

(2) Substances referred to in Subsection (1) include, but are not limited to: (a) gamma butyrolactone (GBL); (b) butyrolactone; (c) 1,2 butanolide; (d) 2-oxanolone; (e) tetrahydro-2-furanone; (f) dihydro-2 (3H)-furanone; (g) tetramethylene glycol; (h) 1,4 butanediol; and (i) gamma valerolactone.

(a) gamma butyrolactone (GBL);

(b) butyrolactone;

(c) 1,2 butanolide;

(d) 2-oxanolone;

(e) tetrahydro-2-furanone;

(f) dihydro-2 (3H)-furanone;

(g) tetramethylene glycol;

(h) 1,4 butanediol; and

(i) gamma valerolactone.

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