1,5-Diiodopentane (stabilized with Copper chip) - ≥98%(GC) , CAS No.628-77-3

CAS: 628-77-3 Cat. No.: D155300 Molecular Weight: 323.94 Beilstein Registry Number: 1(4)317 EC Number: 211-054-1

GRADE & PURITY ≥98%(GC)

Synonyms

PENTANE, 1,5-DIIODO- | BRN 1697281 | FT-0606962 | 4-01-00-00317 (Beilstein Handbook Reference) | 9KQH995EVW | SCHEMBL233429 | IAEOYUUPFYJXHN-UHFFFAOYSA- | Pentamethylene diiodide | J-802016 | C5H10I2 | 1,5-Diiodopentane, 97%, contains copper as stabilizer

Storage

Argon charged,Room temperature

Shipped In

Normal

Overview

Electrochemical reduction of 1,5-diiodopentane at carbon electrodes in DMF containing tetramethylammonium perchlorate has been studied by cyclic voltammetry and controlled-potential electrolysis.1,5-Diiodopentane has been used: · as crosslinking reagent, to investigate the cross-linking layer-by-layer films of bioreducible poly(2-dimethylaminoethyl methacrylate) and DNA · in preparation of (iodoalkylaminocarbene)tungsten complexes

Specifications

Synonyms

PENTANE, 1, 5-DIIODO- | BRN 1697281 | FT-0606962 | 4-01-00-00317 (Beilstein Handbook Reference) | 9KQH995EVW | SCHEMBL233429 | IAEOYUUPFYJXHN-UHFFFAOYSA- | Pentamethylene diiodide | J-802016 | C5H10I2 | 1, 5-Diiodopentane, 97%, contains copper as stabilizer

Specifications & Purity

≥98%(GC)

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥98%(GC)

Names and Identifiers

• Pubchem Sid: 504752312
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752312
• Canonical Smiles: C(CCI)CCI
• IUPAC Name: 1,5-diiodopentane
• InChIKey: IAEOYUUPFYJXHN-UHFFFAOYSA-N
• INCHI: 1S/C5H10I2/c6-4-2-1-3-5-7/h1-5H2
• Isomeric SMILES: C(CCI)CCI
• WGK Germany: 3
• RTECS: SA0425000
• Molecular Weight: 323.94
• Beilstein: 1(4)317
• Reaxy-Rn: 1697281
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1697281&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Class Organoiodides

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Class: Organoiodides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organoiodides
• Alternative Parents: Hydrocarbon derivatives Alkyl iodides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hydrocarbon derivative - Organoiodide - Alkyl iodide - Alkyl halide - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as organoiodides. These are compounds containing a chemical bond between a carbon atom and an iodine 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

Chemical and Physical Properties

• Solubility: Immiscible with water.
• Sensitivity: Air & Light Sensitive
• Refractive Index: 1.6012
• Flash Point(°F): 235.4 °F
• Flash Point(°C): 113 °C
• Boil Point(°C): 102°C/3mmHg
• Melt Point(°C): 9 °C
• Molecular Weight: 323.940 g/mol
• XLogP3: 4.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 4
• Exact Mass: 323.887 Da
• Monoisotopic Mass: 323.887 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 25.300
• 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

References

1. Yunping Wang, Chenlin Mu, Jingtao Bi, Mengmeng Sun, Yingying Zhao.  (2025)  PPY-PEI Engineered Surface With Quaternized Crosslinking for Enhanced K+/Mg2+ Selectivity in Cation Exchange Membranes.  JOURNAL OF APPLIED POLYMER SCIENCE,      [PMID:] [10.1002/app.58016]