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· · COA & SDS available for every product · Same-day shipping on in-stock items 1-Methylpsilocin - ≥99%(HPLC) , CAS No.1465-16-3
Synonyms
1-METHYLPSILOCIN | SCHEMBL12558828 | UNII-65MKC68UST | 1H-Indol-4-ol, 3-[2-(dimethylamino)ethyl]-1-methyl- | BDBM50171261 | 3-[2-(Dimethylamino)ethyl]-1-methyl-1H-indol-4-ol | 3-(2-(Dimethylamino)ethyl)-1-methyl-1H-indol-4-ol | 65MKC68UST | J-008232 | 3-[
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Why this grade ≥99%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
1-METHYLPSILOCIN | SCHEMBL12558828 | UNII-65MKC68UST | 1H-Indol-4-ol, 3-[2-(dimethylamino)ethyl]-1-methyl- | BDBM50171261 | 3-[2-(Dimethylamino)ethyl]-1-methyl-1H-indol-4-ol | 3-(2-(Dimethylamino)ethyl)-1-methyl-1H-indol-4-ol | 65MKC68UST | J-008232 | 3-[
Specifications & Purity
≥99%(HPLC)
Biochemical and Physiological Mechanisms
Potent and selective 5-HT2Cagonist (IC50values are 12 and 633 nM for 5-HT2Cand 5-HT2Areceptors respectively). Displays high affinity for the 5-HT2Breceptor (Ki= 38 nM) but acts as an inverse agonist. Activein vivo; inhibits scratching in a mouse model of
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles CN1C=C(C2=C1C=CC=C2O)CCN(C)C IUPAC Name 3-[2-(dimethylamino)ethyl]-1-methylindol-4-ol InChIKey MZZRFEIDRWKTKJ-UHFFFAOYSA-N INCHI 1S/C13H18N2O/c1-14(2)8-7-10-9-15(3)11-5-4-6-12(16)13(10)11/h4-6,9,16H,7-8H2,1-3H3 Isomeric SMILES CN1C=C(C2=C1C=CC=C2O)CCN(C)C Molecular Weight 218.29 Reaxy-Rn 175070 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=175070&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Class Indoles and derivatives Subclass Tryptamines and derivatives Intermediate Tree Nodes Not available Direct Parent Tryptamines and derivatives Alternative Parents N-alkylindoles Hydroxyindoles 3-alkylindoles Alkaloids and derivatives Aralkylamines 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids N-methylpyrroles Heteroaromatic compounds Trialkylamines Azacyclic compounds Organooxygen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Tryptamine - 3-alkylindole - N-alkylindole - Hydroxyindole - Indole - Alkaloid or derivatives - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - N-methylpyrrole - Benzenoid - Substituted pyrrole - Pyrrole - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organic nitrogen compound - Amine - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as tryptamines and derivatives. These are compounds containing the tryptamine backbone, which is structurally characterized by an indole ring substituted at the 3-position by an ethanamine. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Solvent:DMSO, Max Conc. mg/mL: 21.83, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 2.18, Max Conc. mM: 10 Molecular Weight 218.290 g/mol XLogP3 1.900 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 3 Exact Mass 218.142 Da Monoisotopic Mass 218.142 Da Topological Polar Surface Area 28.400 Ų Heavy Atom Count 16 Formal Charge 0 Complexity 232.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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