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· · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino D-Glucosamic Acid - ≥98% , CAS No.3646-68-2
Synonyms
2-Amino-2-deoxy-D-gluconic acid | OFH5RW45PA | Spectrum_001231 | 1,3-dihydroinden-2-one | Glucosaminic acid | NCGC00178247-01 | SR-05000002429-1 | 6BA699D8-74A0-43AF-82A9-F68E6BFA0B50 | D-lucosamic acid | 2-Amino-2-deoxy-D-gluconate | NSC 404265 | SDCCGML
Storage
Room temperature,Argon charged
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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,Argon charged 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.
Specifications Sinonimi
2-Amino-2-deoxy-D-gluconic acid | OFH5RW45PA | Spectrum_001231 | 1,3-dihydroinden-2-one | Glucosaminic acid | NCGC00178247-01 | SR-05000002429-1 | 6BA699D8-74A0-43AF-82A9-F68E6BFA0B50 | D-lucosamic acid | 2-Amino-2-deoxy-D-gluconate | NSC 404265 | SDCCGML
Condizioni di conservazione di stoccaggio
Room temperature,Argon charged
Nomi e identificatori Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504754713
Sorrisi canonici
C(C(C(C(C(C(=O)O)N)O)O)O)O
IUPAC Name
(2R,3R,4S,5R)-2-amino-3,4,5,6-tetrahydroxyhexanoic acid
InChIKey
UFYKDFXCZBTLOO-TXICZTDVSA-N
INCHI
1S/C6H13NO6/c7-3(6(12)13)5(11)4(10)2(9)1-8/h2-5,8-11H,1,7H2,(H,12,13)/t2-,3-,4-,5-/m1/s1
Isomeri SMILES
C([C@H]([C@H]([C@@H]([C@H](C(=O)O)N)O)O)O)O
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 - Alpha amino acids and derivatives - Alpha amino acids Direct Parent D-alpha-amino acids Alternative Parents Medium-chain hydroxy acids and derivatives Medium-chain fatty acids Amino fatty acids Aminosaccharides Beta hydroxy acids and derivatives Hydroxy fatty acids Monosaccharides 1,3-aminoalcohols Secondary alcohols Amino acids Monocarboxylic acids and derivatives Carboxylic acids Polyols Monoalkylamines Primary alcohols Hydrocarbon derivatives Carbonyl compounds Organic oxides Organopnictogen compounds Molecular Framework Aliphatic acyclic compounds Substituents D-alpha-amino acid - Medium-chain hydroxy acid - Medium-chain fatty acid - Amino fatty acid - Beta-hydroxy acid - Hydroxy fatty acid - Amino saccharide - Hydroxy acid - Fatty acyl - Fatty acid - Monosaccharide - 1,3-aminoalcohol - Amino acid - Secondary alcohol - Carboxylic acid - Monocarboxylic acid or derivatives - Polyol - Primary alcohol - Alcohol - Primary aliphatic amine - Primary amine - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Amine - Organonitrogen compound - Organooxygen compound - Aliphatic acyclic compound Descrizione This compound belongs to the class of organic compounds known as d-alpha-amino acids. These are alpha amino acids which have the D-configuration of the alpha-carbon atom. External Descriptors Uronic 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) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Sensibilità Hygroscopic Rotazione specifica [α] -15° (C=2.5,1mol/L HCl) Peso molecolare 195.170 g/mol XLogP3 -5.900 Hydrogen Bond Donor Count 6 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 5 Exact Mass 195.074 Da Monoisotopic Mass 195.074 Da Topological Polar Surface Area 144.000 Ų Heavy Atom Count 13 Formal Charge 0 Complexity 175.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 4 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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