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· · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino H-Pyr-OH - 10mM in DMSO , CAS No.98-79-3
GRADE & PURITY 10mM in DMSO
Synonyms
L-Pyroglutamic acid|98-79-3|Pidolic acid|Pyroglutamic acid|5-OXOPROLINE|5-oxo-L-proline|H-Pyr-OH|Pyroglutamate|(S)-5-Oxopyrrolidine-2-carboxylic Acid|(2S)-5-oxopyrrolidine-2-carboxylic acid|pyroglu|GLUTIMIC ACID|L-Proline, 5-oxo-|(S)-(-)-2-Pyrrolidone-5-c
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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 32 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Panoramica L-Pyroglutamic acid is a building block for pharmaceuticals and asymmetric synthesis.
Specifications Sinonimi
L-Pyroglutamic acid | 98-79-3 | Pidolic acid | Pyroglutamic acid | 5-OXOPROLINE | 5-oxo-L-proline | H-Pyr-OH | Pyroglutamate | (S)-5-Oxopyrrolidine-2-carboxylic Acid | (2S)-5-oxopyrrolidine-2-carboxylic acid | pyroglu | GLUTIMIC ACID | L-Proline, 5-oxo- | (S)-(-)-2-Pyrrolidone-5-c
Specifiche e purezza
10mM in DMSO
Meccanismi biochimici e fisiologici
Cyclized derivative of L-Glutamic acid. Metabolite in the glutathione cycle.
Condizioni di conservazione di stoccaggio
Store at -80°C
Spedito in
Dry ice packs + Cold packs
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Nomi e identificatori Sorrisi canonici
C1CC(=O)NC1C(=O)O
IUPAC Name
(2S)-5-oxopyrrolidine-2-carboxylic acid
InChIKey
ODHCTXKNWHHXJC-VKHMYHEASA-N
INCHI
1S/C5H7NO3/c7-4-2-1-3(6-4)5(8)9/h3H,1-2H2,(H,6,7)(H,8,9)/t3-/m0/s1
Isomeri SMILES
C1CC(=O)N[C@@H]1C(=O)O
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=82131&ln=
Documentazione 📋 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 Classe Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives Direct Parent Alpha amino acids and derivatives Alternative Parents Pyrroline carboxylic acids Cyclic carboximidic acids Lactims Propargyl-type 1,3-dipolar organic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic heteromonocyclic compounds Substituents Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Pyrroline - Cyclic carboximidic acid - Lactim - Carboxylic acid - Monocarboxylic acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Organoheterocyclic compound - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Organonitrogen compound - Aliphatic heteromonocyclic compound Descrizione This compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. External Descriptors Other amino acids 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.
Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Sensibilità Hygroscopic Rotazione specifica [α] -10 ° (C=5, H2O) Punto di fusione (°C) 152-162°C Peso molecolare 129.110 g/mol XLogP3 -0.800 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 1 Exact Mass 129.043 Da Monoisotopic Mass 129.043 Da Topological Polar Surface Area 66.400 Ų Heavy Atom Count 9 Formal Charge 0 Complexity 154.000 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
Domande frequenti e articoli Citations of This Product Calcolatori di soluzioni Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator Recensioni
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