Adipamide - ≥98%(N) , CAS No.628-94-4

CAS: 628-94-4 Cat. No.: A151413 Summenformel: C₆H₁₂N₂O₂ Molekulargewicht: 144.17 Beilstein Registry Number: 2(4)1972 EG-Nummer: 211-062-5

GRADE & PURITY ≥98%(N)

Synonyms

40DRU033OW | NCGC00091227-02 | WLN: ZV4VZ | CHEBI:165524 | CCRIS 5883 | NCGC00257901-01 | DTXSID4020032 | LMFA08010017 | InChI=1/C6H12N2O2/c7-5(9)3-1-2-4-6(8)10/h1-4H2,(H2,7,9)(H2,8,10) | NSC7623 | NSC-7623 | Adipic acid diamide | MFCD00008045 | 9EE | Adi

Storage

Room temperature,Argon charged

Shipped In

Normal

Übersicht

Adipamide has been used in the preparation of bisimidates

Specifications

Synonyme

40DRU033OW | NCGC00091227-02 | WLN: ZV4VZ | CHEBI:165524 | CCRIS 5883 | NCGC00257901-01 | DTXSID4020032 | LMFA08010017 | InChI=1/C6H12N2O2/c7-5(9)3-1-2-4-6(8)10/h1-4H2,(H2,7,9)(H2,8,10) | NSC7623 | NSC-7623 | Adipic acid diamide | MFCD00008045 | 9EE | Adi

Spezifikationen & Reinheit

≥98%(N)

Storage

Room temperature,Argon charged

Verschickt in

Normal

Reinheit

≥98%(N)

Namen und Kennungen

• Pubchem Sid: 488181638
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181638
• Kanonisches Lächeln: C(CCC(=O)N)CC(=O)N
• IUPAC Name: hexanediamide
• InChIKey: GVNWZKBFMFUVNX-UHFFFAOYSA-N
• INCHI: 1S/C6H12N2O2/c7-5(9)3-1-2-4-6(8)10/h1-4H2,(H2,7,9)(H2,8,10)
• Isomere SMILES: C(CCC(=O)N)CC(=O)N
• WGK Deutschland: 2
• RTECS: AU7800000
• Molekulargewicht: 144.17
• Beilstein: 2(4)1972
• Reaxy-Rn: 1762331
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1762331&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Klasse Fatty Acyls
      • Subclass Fatty amides

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Klasse: Fatty Acyls
• Subclass: Fatty amides
• Intermediate Tree Nodes: Not available
• Direct Parent: Fatty amides
• Alternative Parents: Primary carboxylic acid amides Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fatty amide - Primary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as fatty amides. These are carboxylic acid amide derivatives of fatty acids, that are formed from a fatty acid and an amine.
• 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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Moisture sensitive.
• Schmelzpunkt (°C): 224-228℃
• Molekulargewicht: 144.170 g/mol
• XLogP3: -1.200
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 144.09 Da
• Monoisotopic Mass: 144.09 Da
• Topological Polar Surface Area: 86.200 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 118.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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

Referenzen

1. Yibo Xu, Chenguang Zhou, Jingxuan Xu, Yunlong Yang, Yue Li, Xiangli Wen, Ningyi Yuan, Lvzhou Li, Jianning Ding.  (2026)  An All‑in‑One Bridging Coordination Additive for Scalable, High-Efficiency Perovskite Solar Modules.  Advanced Energy Materials,      [PMID:] [10.1002/aenm.71508]