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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items (S)-(+)-3-Piperidinecarboxylic acid - ≥98% , CAS No.59045-82-8
Synonyms
(3S)-hexahydronicotinic acid | CHEBI:222169 | DB08849 | 2635N2PS4Q | (S)-(+)-Nipecotic acid | SCHEMBL254683 | 4-cis-Hydroxy-L-proline | A8322 | AKOS006238145 | NCGC00024510-01 | (S)-(+)-3-Piperidinecarboxylic acid | Lopac-211672 | L(+)-NIPECOTIC ACID | (+
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping 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 Product Introduction
(S)-(-)-3-Piperidinecarboxylic acid is an inhibitor of GABA (γ-aminobutyric acid) uptake.
Specifications Sinónimos
(3S)-hexahydronicotinic acid | CHEBI:222169 | DB08849 | 2635N2PS4Q | (S)-(+)-Nipecotic acid | SCHEMBL254683 | 4-cis-Hydroxy-L-proline | A8322 | AKOS006238145 | NCGC00024510-01 | (S)-(+)-3-Piperidinecarboxylic acid | Lopac-211672 | L(+)-NIPECOTIC ACID | (+
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Pubchem Sid 504764282 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504764282 Sonrisas canónicas C1CC(CNC1)C(=O)O IUPAC Name (3S)-piperidine-3-carboxylic acid InChIKey XJLSEXAGTJCILF-YFKPBYRVSA-N INCHI 1S/C6H11NO2/c8-6(9)5-2-1-3-7-4-5/h5,7H,1-4H2,(H,8,9)/t5-/m0/s1 Isómeros SMILES C1C[C@@H](CNC1)C(=O)O WGK Alemania 3 Peso molecular 129.16 Beilstein 22(5)1,235 Reaxy-Rn 81096 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=81096&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 Delta amino acids and derivatives Alternative Parents Piperidinecarboxylic acids Carboxylic acid salts Amino acids Monocarboxylic acids and derivatives Dialkylamines Carboxylic acids Azacyclic compounds Organopnictogen compounds Organic zwitterions Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic heteromonocyclic compounds Substituents Delta amino acid or derivatives - Piperidinecarboxylic acid - Piperidine - Carboxylic acid salt - Amino acid - Carboxylic acid - Azacycle - Organoheterocyclic compound - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Secondary amine - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic zwitterion - Organic salt - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Amine - Aliphatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as delta amino acids and derivatives. These are compounds containing a carboxylic acid group and an amino group at the C5 carbon atom. External Descriptors nipecotic acid 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 Rotación específica [α] 5.5° (C=5,H2O) Punto de fusión (°C) 254 °C Peso molecular 129.160 g/mol XLogP3 -2.900 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 1 Exact Mass 129.079 Da Monoisotopic Mass 129.079 Da Topological Polar Surface Area 49.300 Ų Heavy Atom Count 9 Formal Charge 0 Complexity 114.000 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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