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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items (S)-(+)-4-Amino-3-hydroxybutyric acid - ≥97% , CAS No.7013-05-0
Synonyms
S(+)-4-amino-3-hydroxybutanoic acid | A15949 | (+)-gamma-amino-beta-hydroxybutyric acid | AKOS016844198 | (S)-4-Amino-3-hydroxy-butyric acid | gamma-Amino-beta-hydroxybutyric acid, (+)- | (S)-(+)-.BETA.-HYDROXY-GABA | AC-13943 | BDBM50021186 | UNII-CM46XG
Storage
Protected from light,Room temperature
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,Room temperature Ships Normal 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.
Descripción general Description
(S)-(+)-4-Amino-3-hydroxybutyric acid [(S)-GABOB] can be prepared starting from ethyl (S)-4-chloro-3-hydroxybutyrate.
Specifications Sinónimos
S(+)-4-amino-3-hydroxybutanoic acid | A15949 | (+)-gamma-amino-beta-hydroxybutyric acid | AKOS016844198 | (S)-4-Amino-3-hydroxy-butyric acid | gamma-Amino-beta-hydroxybutyric acid, (+)- | (S)-(+)-.BETA.-HYDROXY-GABA | AC-13943 | BDBM50021186 | UNII-CM46XG
Especificaciones y pureza
≥97%
Condiciones de almacenamiento de almacenamiento
Protected from light, Room temperature
Nombres e identificadores Pubchem Sid 488195924 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488195924 Sonrisas canónicas C(C(CN)O)C(=O)O IUPAC Name (3S)-4-amino-3-hydroxybutanoic acid InChIKey YQGDEPYYFWUPGO-VKHMYHEASA-N INCHI 1S/C4H9NO3/c5-2-3(6)1-4(7)8/h3,6H,1-2,5H2,(H,7,8)/t3-/m0/s1 Isómeros SMILES C([C@@H](CN)O)C(=O)O WGK Alemania 3 Peso molecular 119.12 Reaxy-Rn 1721708 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1721708&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 Clase Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives Direct Parent Gamma amino acids and derivatives Alternative Parents Short-chain hydroxy acids and derivatives Beta hydroxy acids and derivatives Fatty acids and conjugates Quaternary ammonium salts Secondary alcohols 1,2-aminoalcohols Amino acids Carboxylic acid salts Monocarboxylic acids and derivatives Carboxylic acids Hydrocarbon derivatives Monoalkylamines Carbonyl compounds Organic oxides Organic salts Organic zwitterions Molecular Framework Aliphatic acyclic compounds Substituents Gamma amino acid or derivatives - Beta-hydroxy acid - Short-chain hydroxy acid - Fatty acid - Hydroxy acid - Quaternary ammonium salt - 1,2-aminoalcohol - Carboxylic acid salt - Amino acid - Secondary alcohol - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Primary amine - Primary aliphatic amine - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Amine - Alcohol - Aliphatic acyclic compound Descripción This compound belongs to the class of organic compounds known as gamma amino acids and derivatives. These are amino acids having a (-NH2) group attached to the gamma carbon atom. 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 Sensibilidad light sensitive；moisture sensitive Punto de fusión (°C) 207-212 °C Peso molecular 119.120 g/mol XLogP3 -4.100 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 3 Exact Mass 119.058 Da Monoisotopic Mass 119.058 Da Topological Polar Surface Area 83.600 Ų Heavy Atom Count 8 Formal Charge 0 Complexity 83.400 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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