Bill Text: IL HB3129 | 2025-2026 | 104th General Assembly | Introduced


Bill Title: Amends the Illinois Controlled Substances Act. Adds mitragynine and 7-hydroxymitragynine as Schedule III controlled substances. Repeals the Kratom Control Act.

Sponsorship: Partisan Bill (Republican 3)

Status: (Introduced - Dead) 2026-02-05 - Added Chief Co-Sponsor Rep. Dave Severin [HB3129 Detail]

Download: Illinois-2025-HB3129-Introduced.html

104TH GENERAL ASSEMBLY
State of Illinois
2025 and 2026
HB3129

Introduced , by Rep. William E Hauter

SYNOPSIS AS INTRODUCED:
720 ILCS 570/208    from Ch. 56 1/2, par. 1208
720 ILCS 642/Act rep.

    Amends the Illinois Controlled Substances Act. Adds mitragynine and 7-hydroxymitragynine as Schedule III controlled substances. Repeals the Kratom Control Act.
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A BILL FOR

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1    AN ACT concerning criminal law.
2    Be it enacted by the People of the State of Illinois,
3represented in the General Assembly:
4    Section 5. The Illinois Controlled Substances Act is
5amended by changing Section 208 as follows:
6    (720 ILCS 570/208)    (from Ch. 56 1/2, par. 1208)
7    Sec. 208. (a) The controlled substances listed in this
8Section are included in Schedule III.
9    (b) Unless specifically excepted or unless listed in
10another schedule, any material, compound, mixture, or
11preparation which contains any quantity of the following
12substances having a stimulant effect on the central nervous
13system, including its salts, isomers (whether optical
14position, or geometric), and salts of such isomers whenever
15the existence of such salts, isomers, and salts of isomers is
16possible within the specific chemical designation;
17        (1) Those compounds, mixtures, or preparations in
18 dosage unit form containing any stimulant substances
19 listed in Schedule II which compounds, mixtures, or
20 preparations were listed on August 25, 1971, as excepted
21 compounds under Title 21, Code of Federal Regulations,
22 Section 308.32, and any other drug of the quantitative
23 composition shown in that list for those drugs or which is

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1 the same except that it contains a lesser quantity of
2 controlled substances;
3        (2) Benzphetamine;
4        (3) Chlorphentermine;
5        (4) Clortermine;
6        (5) Phendimetrazine.
7    (c) Unless specifically excepted or unless listed in
8another schedule, any material, compound, mixture, or
9preparation which contains any quantity of the following
10substances having a potential for misuse associated with a
11depressant effect on the central nervous system:
12        (1) Any compound, mixture, or preparation containing
13 amobarbital, secobarbital, pentobarbital or any salt
14 thereof and one or more other active medicinal ingredients
15 which are not listed in any schedule;
16        (2) Any suppository dosage form containing
17 amobarbital, secobarbital, pentobarbital or any salt of
18 any of these drugs and approved by the Federal Food and
19 Drug Administration for marketing only as a suppository;
20        (3) Any substance which contains any quantity of a
21 derivative of barbituric acid, or any salt thereof:
22        (3.1) Aprobarbital;
23        (3.2) Butabarbital (secbutabarbital);
24        (3.3) Butalbital;
25        (3.4) Butobarbital (butethal);
26        (4) Chlorhexadol;

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1        (5) Methyprylon;
2        (6) Sulfondiethylmethane;
3        (7) Sulfonethylmethane;
4        (8) Sulfonmethane;
5        (9) Lysergic acid;
6        (10) Lysergic acid amide;
7        (10.1) Tiletamine or zolazepam or both, or any salt of
8 either of them.
9    Some trade or other names for a tiletamine-zolazepam
10    combination product: Telazol.
11    Some trade or other names for Tiletamine:
12    2-(ethylamino)-2-(2-thienyl)-cyclohexanone.
13    Some trade or other names for zolazepam:
14    4-(2-fluorophenyl)-6,8-dihydro-1,3,8-trimethylpyrazolo-
15    [3,4-e], [1,4]-diazepin-7(1H)-one, and flupyrazapon.
16        (11) Any material, compound, mixture or preparation
17 containing not more than 12.5 milligrams of pentazocine or
18 any of its salts, per 325 milligrams of aspirin;
19        (12) Any material, compound, mixture or preparation
20 containing not more than 12.5 milligrams of pentazocine or
21 any of its salts, per 325 milligrams of acetaminophen;
22        (13) Any material, compound, mixture or preparation
23 containing not more than 50 milligrams of pentazocine or
24 any of its salts plus naloxone HCl USP 0.5 milligrams, per
25 dosage unit;
26        (14) Ketamine;

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1        (15) Thiopental.
2    (d) Nalorphine.
3    (d.5) Buprenorphine.
4    (e) Unless specifically excepted or unless listed in
5another schedule, any material, compound, mixture, or
6preparation containing limited quantities of any of the
7following narcotic drugs, or their salts calculated as the
8free anhydrous base or alkaloid, as set forth below:
9        (1) not more than 1.8 grams of codeine per 100
10 milliliters or not more than 90 milligrams per dosage
11 unit, with an equal or greater quantity of an isoquinoline
12 alkaloid of opium;
13        (2) not more than 1.8 grams of codeine per 100
14 milliliters or not more than 90 milligrams per dosage
15 unit, with one or more active non-narcotic ingredients in
16 recognized therapeutic amounts;
17        (3) (blank);
18        (4) (blank);
19        (5) not more than 1.8 grams of dihydrocodeine per 100
20 milliliters or not more than 90 milligrams per dosage
21 unit, with one or more active, non-narcotic ingredients in
22 recognized therapeutic amounts;
23        (6) not more than 300 milligrams of ethylmorphine per
24 100 milliliters or not more than 15 milligrams per dosage
25 unit, with one or more active, non-narcotic ingredients in
26 recognized therapeutic amounts;

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1        (7) not more than 500 milligrams of opium per 100
2 milliliters or per 100 grams, or not more than 25
3 milligrams per dosage unit, with one or more active,
4 non-narcotic ingredients in recognized therapeutic
5 amounts;
6        (8) not more than 50 milligrams of morphine per 100
7 milliliters or per 100 grams with one or more active,
8 non-narcotic ingredients in recognized therapeutic
9 amounts.
10    (f) Anabolic steroids, except the following anabolic
11steroids that are exempt:
12        (1) Androgyn L.A.;
13        (2) Andro-Estro 90-4;
14        (3) depANDROGYN;
15        (4) DEPO-T.E.;
16        (5) depTESTROGEN;
17        (6) Duomone;
18        (7) DURATESTRIN;
19        (8) DUO-SPAN II;
20        (9) Estratest;
21        (10) Estratest H.S.;
22        (11) PAN ESTRA TEST;
23        (12) Premarin with Methyltestosterone;
24        (13) TEST-ESTRO Cypionates;
25        (14) Testosterone Cyp 50 Estradiol Cyp 2;
26        (15) Testosterone Cypionate-Estradiol Cypionate

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1 injection; and
2        (16) Testosterone Enanthate-Estradiol Valerate
3 injection.
4    (g) Hallucinogenic substances.
5        (1) Dronabinol (synthetic) in sesame oil and
6 encapsulated in a soft gelatin capsule in a U.S. Food and
7 Drug Administration approved product. Some other names for
8 dronabinol: (6aR-trans)-6a,7,8,10a-tetrahydro-
9 6,6,9-trimethyl-3-pentyl-6H-dibenzo (b,d) pyran-1-ol) or
10 (-)-delta-9-(trans)-tetrahydrocannabinol.
11        (2) (Reserved).
12    (h) The Department may except by rule any compound,
13mixture, or preparation containing any stimulant or depressant
14substance listed in subsection (b) from the application of all
15or any part of this Act if the compound, mixture, or
16preparation contains one or more active medicinal ingredients
17not having a stimulant or depressant effect on the central
18nervous system, and if the admixtures are included therein in
19combinations, quantity, proportion, or concentration that
20vitiate the potential for misuse of the substances which have
21a stimulant or depressant effect on the central nervous
22system.
23    (i) Mitragynine.
24    (j) 7-hydroxymitragynine.    
25(Source: P.A. 103-881, eff. 1-1-25.)

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1    (720 ILCS 642/Act rep.)
2    Section 10. The Kratom Control Act is repealed.
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