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· · COA & SDS available for every product · Same-day shipping on in-stock items L-Tyrosine methyl ester - ≥98% , CAS No.1080-06-4
Synonyms
AKOS000302242 | T-9340 | CCRIS 4038 | MLS000028636 | MFCD00002392 | METHYL (S)-2-AMINO-3-(4-HYDROXYPHENYL)PROPANOATE | (S)-methyl 2-amino-3-(4-hydroxyphenyl)propanoate | (S)-2-Amino-3-(4-hydroxyphenyl)propionic acid methyl ester | (S)-2-Amino-3-(4-hydroxy
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Why this grade ≥98% 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
AKOS000302242 | T-9340 | CCRIS 4038 | MLS000028636 | MFCD00002392 | METHYL (S)-2-AMINO-3-(4-HYDROXYPHENYL)PROPANOATE | (S)-methyl 2-amino-3-(4-hydroxyphenyl)propanoate | (S)-2-Amino-3-(4-hydroxyphenyl)propionic acid methyl ester | (S)-2-Amino-3-(4-hydroxy
Specifications & Purity
≥98%
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Pubchem Sid 488184566 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488184566 Canonical Smiles COC(=O)C(CC1=CC=C(C=C1)O)N IUPAC Name methyl (2S)-2-amino-3-(4-hydroxyphenyl)propanoate InChIKey MWZPENIJLUWBSY-VIFPVBQESA-N INCHI 1S/C10H13NO3/c1-14-10(13)9(11)6-7-2-4-8(12)5-3-7/h2-5,9,12H,6,11H2,1H3/t9-/m0/s1 Isomeric SMILES COC(=O)[C@H](CC1=CC=C(C=C1)O)N WGK Germany 3 Molecular Weight 195.22 Beilstein 2372626 Reaxy-Rn 2110617 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2110617&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 Organic acids and derivatives Class Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives Direct Parent Tyrosine and derivatives Alternative Parents Phenylalanine and derivatives Alpha amino acid esters Amphetamines and derivatives Fatty acid esters Aralkylamines 1-hydroxy-2-unsubstituted benzenoids Methyl esters Monocarboxylic acids and derivatives Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Tyrosine or derivatives - Phenylalanine or derivatives - Alpha-amino acid ester - Amphetamine or derivatives - 1-hydroxy-2-unsubstituted benzenoid - Fatty acid ester - Phenol - Aralkylamine - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Methyl ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxide - Organic nitrogen compound - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Amine - Primary amine - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as tyrosine and derivatives. These are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. External Descriptors L-tyrosyl ester 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 Soluble in water. Sensitivity heat sensitive Specific Rotation[α] 27° (C=1,MeOH) Melt Point(°C) 135-139°C Molecular Weight 195.210 g/mol XLogP3 0.300 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 4 Exact Mass 195.09 Da Monoisotopic Mass 195.09 Da Topological Polar Surface Area 72.600 Ų Heavy Atom Count 14 Formal Charge 0 Complexity 188.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 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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