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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 3-Hydroxyaspartic Acid - ≥98% , CAS No.71653-06-0
Synonyms
DTXSID20875575 | D90978 | Spectrum_001134 | 99A78V5YX2 | H0947 | NSC 84663 | .beta.-erythro-Hydroxy-DL-aspartate | Spectrum2_001914 | A826077 | NSC618260 | NSC-618260 | L-(-)-threo-3-Hydroxyaspartic acid | SPBio_001908 | SPECTRUM501000 | 2-amino-3-hydroxy
Storage
Argon charged,Room temperature
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Argon charged,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.
Specifications Sinónimos
DTXSID20875575 | D90978 | Spectrum_001134 | 99A78V5YX2 | H0947 | NSC 84663 | .beta.-erythro-Hydroxy-DL-aspartate | Spectrum2_001914 | A826077 | NSC618260 | NSC-618260 | L-(-)-threo-3-Hydroxyaspartic acid | SPBio_001908 | SPECTRUM501000 | 2-amino-3-hydroxy
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Argon charged,Room temperature
Nombres e identificadores Pubchem Sid 504750890 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504750890 Sonrisas canónicas C(C(C(=O)O)O)(C(=O)O)N IUPAC Name 2-amino-3-hydroxybutanedioic acid InChIKey YYLQUHNPNCGKJQ-UHFFFAOYSA-N INCHI 1S/C4H7NO5/c5-1(3(7)8)2(6)4(9)10/h1-2,6H,5H2,(H,7,8)(H,9,10) Isómeros SMILES C(C(C(=O)O)O)(C(=O)O)N Peso molecular 149.1 Reaxy-Rn 1101761 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1101761&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 - Alpha amino acids and derivatives Direct Parent Aspartic acid and derivatives Alternative Parents Alpha amino acids Short-chain hydroxy acids and derivatives Beta hydroxy acids and derivatives Monosaccharides Fatty acids and conjugates Dicarboxylic acids and derivatives Alpha hydroxy acids and derivatives Secondary alcohols Amino acids Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic acyclic compounds Substituents Aspartic acid or derivatives - Alpha-amino acid - Beta-hydroxy acid - Short-chain hydroxy acid - Alpha-hydroxy acid - Dicarboxylic acid or derivatives - Fatty acid - Hydroxy acid - Monosaccharide - Amino acid - Secondary alcohol - Carboxylic acid - Alcohol - Organonitrogen compound - Organooxygen compound - Primary aliphatic amine - Primary amine - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organopnictogen compound - Amine - Organic oxygen compound - Organic nitrogen compound - Aliphatic acyclic compound Descripción This compound belongs to the class of organic compounds known as aspartic acid and derivatives. These are compounds containing an aspartic acid or a derivative thereof resulting from reaction of aspartic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. External Descriptors C4-dicarboxylic acid - amino dicarboxylic acid - hydroxy-amino acid - aspartic acid derivative 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) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Sensibilidad air sensitive Peso molecular 149.100 g/mol XLogP3 -4.400 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 3 Exact Mass 149.032 Da Monoisotopic Mass 149.032 Da Topological Polar Surface Area 121.000 Ų Heavy Atom Count 10 Formal Charge 0 Complexity 156.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 2 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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