| Identification | Back Directory | [Name]
5-hydroxy DMT (hydrochloride) | [CAS]
55206-22-9 | [Synonyms]
Bufotenine Hydrochloride
5-hydroxy DMT (hydrochloride)
5-hydroxy DMT (hydrochloride) (exempt preparation)
3-[2-(dimethylamino)ethyl]-1H-indol-5-ol:hydrochloride | [Molecular Formula]
C12H17ClN2O | [MOL File]
55206-22-9.mol | [Molecular Weight]
240.73 |
| Chemical Properties | Back Directory | [Melting point ]
>60°C (dec.) | [storage temp. ]
Hygroscopic, -20°C Freezer, Under inert atmosphere | [solubility ]
Methanol (Slightly), Water (Slightly) | [form ]
Solid | [color ]
Light Beige to Very Dark Brown | [Stability:]
Very Hygroscopic |
| Hazard Information | Back Directory | [Description]
5-hydroxy DMT (hydrochloride) (exempt preparation) (Item No. 15693) is an analytical reference standard categorized as a tryptamine. 5-hydroxy DMT is an active metabolite of 5-methoxy DMT (Item Nos. 11480 | 11628). 5-hydroxy DMT is regulated as a Schedule I compound in the United States. 5-hydroxy DMT (hydrochloride) (exempt preparation) (Item No. 15693) is provided as a DEA exempt preparation. This product is intended for research and forensic applications. | [Uses]
5-hydroxy DMT is a tryptamine compound first isolated from toad skin. It is similar in structure to the serotonergic mimics 4-hydroxy DMT and 5-methoxy DMT and can affect both central and peripheral serotonin receptors. 5-hydroxy DMT binds to the 5-HT2A receptor with much greater affinity than 5-methoxy DMT and has also been reported to have mild MAO inhibiting effects. This product is listed as a Schedule I compound in the US and intended only for forensic and research applications.[Cayman Chemical] | [References]
[1] B L ROTH. High-affinity agonist binding is not sufficient for agonist efficacy at 5-hydroxytryptamine2A receptors: evidence in favor of a modified ternary complex model.[J]. Journal of Pharmacology and Experimental Therapeutics, 1997, 280 2: 576-583.
[2] HONG-WU SHEN. Psychedelic 5-methoxy-N,N-dimethyltryptamine: metabolism, pharmacokinetics, drug interactions, and pharmacological actions.[J]. Current drug metabolism, 2010, 11 8: 659-666. DOI: 10.2174/138920010794233495
[3] MARTIN J SPIERING E E James F Parsons. On the Biosynthesis of Bioactive Tryptamines in Black Cohosh (Actaea racemosa L.).[J]. Plants-Basel, 2025, 14 2. DOI: 10.3390/plants14020292 |
|
| Company Name: |
Energy Chemical
|
| Tel: |
021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
|