As of November 12, 2026, 9-OH (9-hydroxycorynantheidine) is legal to sell at retail with restrictions in Nevada. Kratom law sets 18+, labeling and anti-adulteration rules; reaches a synthetic product that contains mitragynine or 7-OH (NRS 597.998). Controlling source: NRS 597.998 (kratom products: sale to minors, adulteration, labeling).
Verified November 12, 2026 (hash check) · confidence: under reviewIs 9-OH Legal? Every state and federal law
Nevada does not name 9-hydroxycorynantheidine (9-OH, 9-O-demethylmitragynine), mitragynine, 7-hydroxymitragynine or kratom in Schedule I (NAC 453.510, NAC chapter 453 revised 8-26-2026), and no class listing or whole-plant ban reaches kratom alkaloids. NRS 597.998 (A.B. 303, 2019) is the state kratom law. It bars knowingly selling a material containing a kratom product to a child under 18, bars preparing or selling a kratom product adulterated to a degree that renders it injurious, and requires a label setting out ingredients and directions for safe and effective use, with a civil penalty of up to 1,000 dollars per violation. It sets no registration, testing, form rule, 7-OH cap or synthetic-alkaloid ban. A kratom product is any product or ingredient containing leaf of Mitragyna speciosa that contains mitragynine or 7-OH, or a synthetic material that contains mitragynine or 7-OH. A semi-synthetic 9-OH tablet or liquid is not leaf, so the conditions reach it only if it contains residual mitragynine or 7-OH; whether a product free of both is covered is definitional, and confidence is under review on that point. NRS 453.043 and 453.219 treat a controlled substance analog intended for human consumption as Schedule I, but the definition requires structural similarity to a Schedule I or II substance, and Nevada schedules no kratom alkaloid, so analog reach is remote. NRS 453.2182 has the Board similarly treat federally scheduled substances; 9-OH is not federally scheduled. The Board took public comment in 2026 on scheduling mitragynine; no regulation was found. A mitragynine listing with isomer, ester, ether and salt words would not plainly reach 9-OH. The Legislature next meets in February 2027. 9-OH is not federally scheduled; federal Analogue Act and FDA exposure are interpretive.
1. A person shall not knowingly sell or offer to sell any material, compound, mixture or preparation containing a kratom product to a child under the age of 18 years. ... 3. A person shall not sell a kratom product that does not have a label that clearly sets forth the ingredients and directions for the safe and effective use of the kratom product. ... 5. As used in this section, kratom product means any product or ingredient containing: (a) Any part of the leaf of the Mitragyna Speciosa plant if the plant contains the alkaloid mitragynine or 7-hydroxymitragynine; or (b) A synthetic material that contains the alkaloid mitragynine or 7-hydroxymitragynine, regardless of whether the product or ingredient is labeled or sold for human consumption. ... 2. Unless specifically excepted or unless listed in another schedule, any of the following opiates, including, without limitation, their isomers, esters, ethers, salts and salts of isomers, esters and ethers, whenever the existence of such isomers, esters, ethers and salts is possible within the specific chemical designation:
Among Nevada’s 5 neighbors, Oregon is restricted; Arizona, California and Utah are gray area; Idaho is legal.
Open the interactive map · Every compound in Nevada · Where 9-OH is banned · Embed this map
Not federally scheduled. Not federally scheduled: absent from 21 CFR 1308.11 and every DEA kratom-alkaloid order and notice; Analogue Act exposure is interpretive Federal detail
3 instruments on file for this compound’s framework in Nevada; 4 of 4 citations above are official sources. Each text carries its source and a fingerprint that changes when the law does.
a19a9e9f0c3f84d01. A person shall not knowingly sell or offer to sell any material, compound, mixture or preparation containing a kratom product to a child under the age of 18 years. 2. A person shall not knowingly prepare, distribute, advertise, sell or offer to sell a kratom product that is adulterated with a substance that affects the quality or strength of the kratom product to such a degree as to render the kratom product injurious to a consumer. A person has not violated the provisions of this subsection if he or she can show by a preponderance of evidence that he or she relied in good faith upon the representations of a manufacturer, processor, packer or distributor of the kratom product. 3. A person shall not sell a kratom product that does not have a label that clearly sets forth the ingredients and directions for the safe and effective use of the kratom product. 4. A person who violates any provision of this section is subject to a civil penalty of not more than $1,000 for each violation. 5. As used in this section, "kratom product" means any product or ingredient containing: (a) Any part of the leaf of the Mitragyna Speciosa plant if the plant contains the alkaloid mitragynine or 7-hydroxymitragynine; or (b) A synthetic material that contains the alkaloid mitragynine or 7-hydroxymitragynine, regardless of whether the product or ingredient is labeled or sold for human consumption.
35761c7f56e58bf8453.2182 Treatment by Board when substance is designated, rescheduled or deleted as controlled substance by federal law. If a substance is designated, rescheduled or deleted as a controlled substance pursuant to federal law, the Board shall similarly treat the substance pursuant to the provisions of NRS 453.011 to 453.552 , inclusive, after the expiration of 60 days from publication in the Federal Register of a final order designating a substance as a controlled substance or rescheduling or deleting a substance or from the date of issuance of an order of temporary scheduling under Section 508 of the federal Dangerous Drug Diversion Control Act of 1984, 21 U.S.C. § 811(h), unless within the 60-day period, the Board or an interested party objects to the treatment of the substance. If no objection is made, the Board shall adopt, without making the determinations or findings required by subsections 1 to 4, inclusive, of NRS 453.146 or NRS 453.166 , 453.176 , 453.186 , 453.196 or 453.206 , a final regulation treating the substance. If an objection is made, the Board shall make a determination with respect to the treatment of the substance as provided by subsections 1 to 4, inclusive, of NRS 453.146 . Upon receipt of an objection to the treatment by the Board, the Board shall publish notice of the receipt of the objection, and action by the Board is stayed until the Board adopts a regulation as provided by subsection 4 of NRS 453.146 . (Added to NRS by 1991, 1644 ; A 2001, 1056 ; 2003, 552 )
a00a1ecc5ae992bd1. A person shall not knowingly sell or offer to sell any material, compound, mixture or preparation containing a kratom product to a child under the age of 18 years. 2. A person shall not knowingly prepare, distribute, advertise, sell or offer to sell a kratom product that is adulterated with a substance that affects the quality or strength of the kratom product to such a degree as to render the kratom product injurious to a consumer. A person has not violated the provisions of this subsection if he or she can show by a preponderance of evidence that he or she relied in good faith upon the representations of a manufacturer, processor, packer or distributor of the kratom product. 3. A person shall not sell a kratom product that does not have a label that clearly sets forth the ingredients and directions for the safe and effective use of the kratom product. 4. A person who violates any provision of this section is subject to a civil penalty of not more than $1,000 for each violation. 5. As used in this section, kratom product means any product or ingredient containing: (a) Any part of the leaf of the Mitragyna Speciosa plant if the plant contains the alkaloid mitragynine or 7-hydroxymitragynine; or (b) A synthetic material that contains the alkaloid mitragynine or 7-hydroxymitragynine, regardless of whether the product or ingredient is labeled or sold for human consumption.
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