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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items (RS)-3-Hydroxyphenylglycine - ≥98% , CAS No.31932-87-3
Synonyms
Amino(3-hydroxyphenyl)acetic acid | (RS)-3-HYDROXYPHENYLGLYCINE | DL-2-(3-Hydroxyphenyl)glycine | (R)-AMINO-(3-HYDROXY-PHENYL)-ACETIC ACID | (S)-(3-Hydroxyphenyl)glycine | 3HPG | m-Hydroxyphenylglycine | 2-Amino-2-(3-hydroxyphenyl)acetic acid | 2-(3-hydro
Storage
Store at -20°C,Desiccated
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 Store at -20°C,Desiccated 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.
Specifications Sinónimos
Amino(3-hydroxyphenyl)acetic acid | (RS)-3-HYDROXYPHENYLGLYCINE | DL-2-(3-Hydroxyphenyl)glycine | (R)-AMINO-(3-HYDROXY-PHENYL)-ACETIC ACID | (S)-(3-Hydroxyphenyl)glycine | 3HPG | m-Hydroxyphenylglycine | 2-Amino-2-(3-hydroxyphenyl)acetic acid | 2-(3-hydro
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Agonist at PI-linked metabotropic glutamate receptors.S-enantiomeralso available.
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Desiccated
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Sonrisas canónicas C1=CC(=CC(=C1)O)C(C(=O)O)N IUPAC Name 2-amino-2-(3-hydroxyphenyl)acetic acid InChIKey DQLYTFPAEVJTFM-UHFFFAOYSA-N INCHI 1S/C8H9NO3/c9-7(8(11)12)5-2-1-3-6(10)4-5/h1-4,7,10H,9H2,(H,11,12) Isómeros SMILES C1=CC(=CC(=C1)O)C(C(=O)O)N PubChem CID 1217 Peso molecular 167.16
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 Clase Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives Direct Parent Alpha amino acids Alternative Parents Aralkylamines 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Alpha-amino acid - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Primary amine - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Primary aliphatic amine - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Amine - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Solvent:1eq. NaOH, Max Conc. mg/mL: None, Max Conc. mM: 100 Peso molecular 167.160 g/mol XLogP3 -2.100 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 2 Exact Mass 167.058 Da Monoisotopic Mass 167.058 Da Topological Polar Surface Area 83.600 Ų Heavy Atom Count 12 Formal Charge 0 Complexity 172.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 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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