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≥98%(GC), stabilized with copper for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
1,6-Diiodohexane has been used:
• in preparation of cationic tissue plasminogen activator (t-PA)-containing polyurethane surfaces
• as solvent additive, to improve the power conversion effciency of polymer/fullerene bulk heterojunction solar cells
• synthesis of new macrocycles, having 2,4-dihydroxybenzophenone as a connecting unit
• preparation of a novel ionic electrolyte, 3-(iodohexyl)-1-(3-(triethoxysilyl)propylcarbamoyl)-1H-benzo[d]imidazol-3-ium iodide
| Pubchem Sid | 504752318 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504752318 |
| Sonrisas canónicas | C(CCCI)CCI |
| IUPAC Name | 1,6-diiodohexane |
| InChIKey | QLIMAARBRDAYGQ-UHFFFAOYSA-N |
| INCHI | 1S/C6H12I2/c7-5-3-1-2-4-6-8/h1-6H2 |
| Isómeros SMILES | C(CCCI)CCI |
| WGK Alemania | 3 |
| RTECS | MO1700000 |
| Peso molecular | 337.97 |
| Beilstein | 1147 |
| Reaxy-Rn | 1280128 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1280128&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organohalogen compounds |
| Clase | 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 |
| Descripción | 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 |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Jun 08, 2026 | D119377 | |
| Certificate of Analysis | Jun 08, 2026 | D119377 | |
| Certificate of Analysis | Mar 09, 2026 | D119377 | |
| Certificate of Analysis | Mar 09, 2026 | D119377 | |
| Certificate of Analysis | Mar 09, 2026 | D119377 | |
| Certificate of Analysis | Apr 02, 2025 | D119377 | |
| Certificate of Analysis | Apr 02, 2025 | D119377 | |
| Certificate of Analysis | Apr 02, 2025 | D119377 | |
| Certificate of Analysis | Apr 02, 2025 | D119377 | |
| Certificate of Analysis | May 12, 2023 | D119377 | |
| Certificate of Analysis | May 12, 2023 | D119377 | |
| Certificate of Analysis | Jan 18, 2023 | D119377 |
| Solubilidad | Immiscible with water. |
|---|---|
| Sensibilidad | Air & light Sensitive |
| Índice de refracción | n20/D 1.5852(lit.) |
| Punto de inflamación (°F) | 235.4 °F |
| Punto de inflamación (°C) | >110°(230°F) |
| Punto de ebullición (°C) | 141-142°C/10mmHg |
| Punto de fusión (°C) | 9-10°C |
| Peso molecular | 337.970 g/mol |
| XLogP3 | 4.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 5 |
| Exact Mass | 337.903 Da |
| Monoisotopic Mass | 337.903 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 31.500 |
| 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 |
| 1. Ganggang Zhang, Chenchen Tian, Heying Chu, Jun Liu, Baochun Guo, Liqun Zhang. (2023) A facile strategy to achieve vitrimer-like elastomer composites with lignin as a renewable bio-filler toward excellent reinforcement and recyclability. Journal of Materials Chemistry A, 11 (46): (25356-25367). [PMID:] [10.1039/D3TA05205B] |
| 2. Jun Zhang, Rongye Guo, Yubing Li, Hanyu Ma, Junkun Tang, Zuozhen Liu, Farong Huang. (2023) Effect of halogenated hydrocarbon crosslinkers on self-healing poly(1,2,3-triazolium) adhesives. POLYMER, [PMID:] [10.1016/j.polymer.2023.126192] |
| 3. Zhaofei Wang, Xuemin Zhang, Wansheng Yao, Yong Dong, Baiyao Zhang, Xiaoyu Dong, Huagao Fang, Guobing Zhang, Yunsheng Ding. (2022) Dynamically Cross-Linked Waterborne Polyurethanes: Transalkylation Exchange of C–N Bonds Toward High Performance and Reprocessable Thermosets. ACS Applied Polymer Materials, [PMID:] [10.1021/acsapm.2c00794] |