3-Aminopiperidine-2,6-dione - ≥95% , CAS No.2353-44-8

CAS: 2353-44-8 Cat. No.: A588312 Molecular Weight: 128.13

GRADE & PURITY ≥95%

Synonyms

Abcid | AS-38862 | 3-amino-1,6-dioxopiperidine | AKOS006240017 | SY258364 | DTXSID50946287 | SB21747 | 2,6-Piperidinedione, 3-amino- | 3-Amino-6-hydroxy-4,5-dihydropyridin-2(3H)-one | sulphamethazole | pyroglutamine | 3-AMINO-PIPERIDINE-2,6-DIONE | 3-amin

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice

Specifications

Synonyms

Abcid | AS-38862 | 3-amino-1, 6-dioxopiperidine | AKOS006240017 | SY258364 | DTXSID50946287 | SB21747 | 2, 6-Piperidinedione, 3-amino- | 3-Amino-6-hydroxy-4, 5-dihydropyridin-2(3H)-one | sulphamethazole | pyroglutamine | 3-AMINO-PIPERIDINE-2, 6-DIONE | 3-amin

Specifications & Purity

≥95%

Storage

Store at 2-8°C, Protected from light, Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥95%

Names and Identifiers

• Pubchem Sid: 504757028
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504757028
• Canonical Smiles: C1CC(=O)NC(=O)C1N
• IUPAC Name: 3-aminopiperidine-2,6-dione
• InChIKey: NPWMTBZSRRLQNJ-UHFFFAOYSA-N
• INCHI: 1S/C5H8N2O2/c6-3-1-2-4(8)7-5(3)9/h3H,1-2,6H2,(H,7,8,9)
• Isomeric SMILES: C1CC(=O)NC(=O)C1N
• Molecular Weight: 128.13
• Reaxy-Rn: 81982
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=81982&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: 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: Piperidinediones Delta lactams Aminopiperidines N-unsubstituted carboxylic acid imides Dicarboximides Azacyclic compounds Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Alpha-amino acid or derivatives - Piperidinedione - 3-aminopiperidine - Delta-lactam - Piperidinone - Piperidine - Carboxylic acid imide - Dicarboximide - Carboxylic acid imide, n-unsubstituted - Lactam - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Amine - Organooxygen compound - Primary amine - Aliphatic heteromonocyclic compound
• Description: 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: Not available

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.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Light sensitive
• Molecular Weight: 128.130 g/mol
• XLogP3: -1.500
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 128.059 Da
• Monoisotopic Mass: 128.059 Da
• Topological Polar Surface Area: 72.200 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 155.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Siyu Guo, Xueting Ren, Xijiao Ren, Jinming He, Huocheng Yang, Wei Zhou, Menghuan Li, Lulu Wang, Yan Hu, Zhong Luo.  (2026)  Supramolecular DNA Di-Tetrahedral Neoadjuvants Dynamically Prime Melanoma Microenvironment for Enhancing Radio-Immunotherapy Responses.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202524385]