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· · COA & SDS available for every product · Same-day shipping on in-stock items 3-Methoxytyramine hydrochloride(3-MT) - ≥98% , CAS No.1477-68-5
Synonyms
3-MT | 3-MT | 5-(2-Aminoethyl)guaiacol HCl | MFCD00012902 | SY062385 | 13,14-dihydro Prostaglandin F2 alpha | DTXSID801017284 | PD021165 | NSC 172190 | AWRIOTVUTPLWLF-UHFFFAOYSA-N | MLS002153361 | 3-Methoxytyramine (hydrochloride) | DTXSID40163784 | UNII-
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,Store at -20°C Ships Ice chest + Ice pads 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.
Overview Product description：
3-Methoxytyramine hydrochloride is an inactive metabolite of dopamine which can activate trace amine associated receptor 1 (TAAR1).
Specifications Synonyms
3-MT | 3-MT | 5-(2-Aminoethyl)guaiacol HCl | MFCD00012902 | SY062385 | 13, 14-dihydro Prostaglandin F2 alpha | DTXSID801017284 | PD021165 | NSC 172190 | AWRIOTVUTPLWLF-UHFFFAOYSA-N | MLS002153361 | 3-Methoxytyramine (hydrochloride) | DTXSID40163784 | UNII-
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
The main metabolite of dopamine; Catechol O-methyltransferase product.
Storage
Protected from light, Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles COC1=C(C=CC(=C1)CCN)O.Cl IUPAC Name 4-(2-aminoethyl)-2-methoxyphenol;hydrochloride InChIKey AWRIOTVUTPLWLF-UHFFFAOYSA-N INCHI 1S/C9H13NO2.ClH/c1-12-9-6-7(4-5-10)2-3-8(9)11;/h2-3,6,11H,4-5,10H2,1H3;1H Isomeric SMILES COC1=C(C=CC(=C1)CCN)O.Cl WGK Germany 3 Molecular Weight 203.67 Beilstein 3631283 Reaxy-Rn 3631283 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3631283&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 Benzenoids Class Phenols Subclass Methoxyphenols Intermediate Tree Nodes Not available Direct Parent Methoxyphenols Alternative Parents Phenethylamines Phenoxy compounds Methoxybenzenes Anisoles Aralkylamines Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Quaternary ammonium salts Organic zwitterions Organic chloride salts Monoalkylamines Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Methoxyphenol - Phenethylamine - Anisole - Phenoxy compound - Phenol ether - Methoxybenzene - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Alkyl aryl ether - Monocyclic benzene moiety - Quaternary ammonium salt - Ether - Primary amine - Organic zwitterion - Amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic nitrogen compound - Organic salt - Hydrocarbon derivative - Organic oxygen compound - Organic chloride salt - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as methoxyphenols. These are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. 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) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility ≥10.3 mg/mL in EtOH; ≥44.7 mg/mL in H2O; ≥49.4 mg/mL in DMSO Sensitivity Moisture sensitive；Light sensitive Molecular Weight 203.660 g/mol XLogP3 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 3 Exact Mass 203.071 Da Monoisotopic Mass 203.071 Da Topological Polar Surface Area 55.500 Ų Heavy Atom Count 13 Formal Charge 0 Complexity 130.000 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 2
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