5-Aminovaleric Acid Hydroiodide (Low water content) - ≥97% , CAS No.1705581-28-7

CAS: 1705581-28-7 Cat. No.: A151151 Peso molecular: 245.06 Número EC: 835-031-6

GRADE & PURITY ≥97%

Synonyms

5-Aminovaleric acid hydroiodide | T70410 | 1705581-28-7 | 5-aminopentanoic acid;hydroiodide | Homopiperidinic Acid Hydroiodide | SCHEMBL17025870 | MFCD30470493 | 5-Aminovaleric Acid Hydroiodide (Low water content) | 5-Aminopentanoic Acid Hydroiodide | 5-A

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Sinónimos

5-Aminovaleric acid hydroiodide | T70410 | 1705581-28-7 | 5-aminopentanoic acid;hydroiodide | Homopiperidinic Acid Hydroiodide | SCHEMBL17025870 | MFCD30470493 | 5-Aminovaleric Acid Hydroiodide (Low water content) | 5-Aminopentanoic Acid Hydroiodide | 5-A

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥97%

Nombres e identificadores

• Sonrisas canónicas: C(CCN)CC(=O)O.I
• IUPAC Name: 5-aminopentanoic acid;hydroiodide
• InChIKey: QRCPJIVRDACIKP-UHFFFAOYSA-N
• INCHI: 1S/C5H11NO2.HI/c6-4-2-1-3-5(7)8;/h1-4,6H2,(H,7,8);1H
• Isómeros SMILES: C(CCN)CC(=O)O.I
• Peso molecular: 245.06
• Reaxy-Rn: 32855170
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=32855170&ln=

Taxonomic Classification

Taxonomy Tree

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

• 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
• Direct Parent: Delta amino acids and derivatives
• Alternative Parents: Straight chain fatty acids Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Delta amino acid or derivatives - Fatty acyl - Fatty acid - Straight chain fatty acid - Amino acid - Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as delta amino acids and derivatives. These are compounds containing a carboxylic acid group and an amino group at the C5 carbon atom.
• 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

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive
• Peso molecular: 245.060 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 244.991 Da
• Monoisotopic Mass: 244.991 Da
• Topological Polar Surface Area: 63.300 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 72.800
• 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: 2

XLogP3

Referencias

1. Shuojian Su, Haifei Wang, Yugang Liang, Yuetian Chen, Yanfeng Miao, Yixin Zhao.  (2026)  Bifunctional molecular interface spacer for high-efficiency and stable large-area perovskite solar modules.  Journal of Energy Chemistry,      [PMID:] [10.1016/j.jechem.2026.01.039]