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| | 1H-Indole-3-ethanamine, 5-methoxy-N,N-dimethyl-, (2E)-2-butenedioate (1:1) Basic information |
| | 1H-Indole-3-ethanamine, 5-methoxy-N,N-dimethyl-, (2E)-2-butenedioate (1:1) Chemical Properties |
| solubility | DMF: 20 mg/ml DMSO: 30 mg/ml Ethanol: 5 mg/mlPBS (pH 7.2): 3 mg/ml |
| | 1H-Indole-3-ethanamine, 5-methoxy-N,N-dimethyl-, (2E)-2-butenedioate (1:1) Usage And Synthesis |
| Description | 5-methoxy DMT (fumarate) (Item No. 35025) is an analytical reference standard categorized as a tryptamine.1 5-methoxy DMT induces the head-twitch response (HTR) in mice, indicating hallucinogenic potential. 5-methoxy DMT substitutes for LSD (Item Nos. 35189 | 28289) in a two-key drug discrimination test.2 5-methoxy DMT is regulated as a Schedule I compound in the United States. This product is intended for research and forensic applications.WARNING This product is not for human or veterinary use. | | References | [1] C SINGLETON C A M. Circadian variation in the head twitch response produced by 5-methoxy-N1,N1-dimethyltryptamine and p-chloroamphetamine in the mouse.[J]. Psychopharmacology, 1981, 74 2: 173-176. DOI: 10.1007/bf00432688 [2] NIELSEN E B. Discriminative stimulus properties of lysergic acid diethylamide in the monkey.[J]. Journal of Pharmacology and Experimental Therapeutics, 1985, 234 1: 244-249.
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| | 1H-Indole-3-ethanamine, 5-methoxy-N,N-dimethyl-, (2E)-2-butenedioate (1:1) Preparation Products And Raw materials |
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