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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 2-Keto-L-gulonic Acid - Moligand™,≥98% , CAS No.526-98-7
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98% Synonyms
E72647 | VBUYCZFBVCCYFD-NUNKFHFFSA-N | 2-dehydro-L-idonic acid | Phenyl Ethanol(Natural) | Q27109187 | 6DBA7178-9A91-4E10-8B9E-22EBA19458C8 | EINECS 208-403-5 | 2-Keto-L-gulonic acid | I49386U15C | 2-Oxo-l-gulonic acid | L-sorbosonate | Ach;ACh chloride |
Storage
Store at 2-8°C,Protected from light,Argon charged
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Why this grade Moligand™,≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Protected from light,Argon charged 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.
Descripción general Product Application:
2-Keto-L-gulonic Acid is used in biological studies for the formation of sorbitol metabolism by Acetobacter melanogenus.
Specifications Sinónimos
E72647 | VBUYCZFBVCCYFD-NUNKFHFFSA-N | 2-dehydro-L-idonic acid | Phenyl Ethanol(Natural) | Q27109187 | 6DBA7178-9A91-4E10-8B9E-22EBA19458C8 | EINECS 208-403-5 | 2-Keto-L-gulonic acid | I49386U15C | 2-Oxo-l-gulonic acid | L-sorbosonate | Ach;ACh chloride |
Especificaciones y pureza
Moligand™, ≥98%
Mecanismos bioquímicos y fisiológicos
2-Keto-L-gulonic acid (2-KLG) is a crucial precursor in the industrial production of vitamin C. 2-Keto-L-gulonic acid inhibits the growth of Bacillus pumilus and Ketogulonicigenium vulgare.
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Protected from light, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Pubchem Sid 488187297 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488187297 Sonrisas canónicas C(C(C(C(C(=O)C(=O)O)O)O)O)O IUPAC Name (3S,4R,5S)-3,4,5,6-tetrahydroxy-2-oxohexanoic acid InChIKey VBUYCZFBVCCYFD-NUNKFHFFSA-N INCHI 1S/C6H10O7/c7-1-2(8)3(9)4(10)5(11)6(12)13/h2-4,7-10H,1H2,(H,12,13)/t2-,3+,4-/m0/s1 Isómeros SMILES C([C@@H]([C@H]([C@@H](C(=O)C(=O)O)O)O)O)O Peso molecular 194.14 Reaxy-Rn 2211532 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2211532&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 oxygen compounds Clase Organooxygen compounds Subclass Carbohydrates and carbohydrate conjugates Intermediate Tree Nodes Not available Direct Parent Sugar acids and derivatives Alternative Parents Hexoses Medium-chain keto acids and derivatives Beta hydroxy acids and derivatives Beta-hydroxy ketones Alpha-keto acids and derivatives Acyloins Alpha-hydroxy ketones Secondary alcohols Polyols Monocarboxylic acids and derivatives Carboxylic acids Primary alcohols Organic oxides Hydrocarbon derivatives Molecular Framework Aliphatic acyclic compounds Substituents Hexose monosaccharide - Medium-chain keto acid - Beta-hydroxy acid - Sugar acid - Acyloin - Alpha-keto acid - Beta-hydroxy ketone - Hydroxy acid - Keto acid - Monosaccharide - Alpha-hydroxy ketone - Ketone - Secondary alcohol - Carboxylic acid - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Polyol - Alcohol - Hydrocarbon derivative - Carbonyl group - Organic oxide - Primary alcohol - Aliphatic acyclic compound Descripción This compound belongs to the class of organic compounds known as sugar acids and derivatives. These are compounds containing a saccharide unit which bears a carboxylic acid group. External Descriptors ketoaldonic 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 Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Sensibilidad Hygroscopic Punto de fusión (°C) >125ºC Peso molecular 194.140 g/mol XLogP3 -2.900 Hydrogen Bond Donor Count 5 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 5 Exact Mass 194.043 Da Monoisotopic Mass 194.043 Da Topological Polar Surface Area 135.000 Ų Heavy Atom Count 13 Formal Charge 0 Complexity 201.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 3 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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Reconstitution Calculator Reseñas Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
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