≥98%(GC), stabilized with Copper for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice 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 6 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
The standard molar enthalpy of 2-iodoethanol formation has been studied.
2-Iodoethanol is used in the synthesis of the neuroexcitants 3-(carboxymethyl)pyrrolidine-2,4-dicarboxylic acid, α-kainic acid, alpha-isokainic acid and alpha-dihydroallokainic acid.
| Pubchem Sid | 488181588 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488181588 |
| Sonrisas canónicas | C(CI)O |
| IUPAC Name | 2-iodoethanol |
| InChIKey | QSECPQCFCWVBKM-UHFFFAOYSA-N |
| INCHI | 1S/C2H5IO/c3-1-2-4/h4H,1-2H2 |
| Isómeros SMILES | C(CI)O |
| WGK Alemania | 3 |
| RTECS | KL3820000 |
| Peso molecular | 171.97 |
| Beilstein | 1339 |
| Reaxy-Rn | 1098258 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098258&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 | Halohydrins |
| Subclass | Iodohydrins |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Iodohydrins |
| Alternative Parents | Primary alcohols Organoiodides Hydrocarbon derivatives Alkyl iodides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Iodohydrin - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organoiodide - Alkyl iodide - Alkyl halide - Alcohol - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as iodohydrins. These are alcohols substituted by a iodine atom at a saturated carbon atom otherwise bearing only hydrogen or hydrocarbyl groups. |
| 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 |
|---|---|---|---|
 L2518056 | Certificate of Analysis | Dec 30, 2025 | I137311 |
| F2526068 | Certificate of Analysis | Jul 02, 2025 | I137311 |
| G2326694 | Certificate of Analysis | May 09, 2025 | I137311 |
| G2326699 | Certificate of Analysis | May 09, 2025 | I137311 |
| G2326706 | Certificate of Analysis | May 09, 2025 | I137311 |
| E2305330 | Certificate of Analysis | Feb 07, 2025 | I137311 |
| E2305331 | Certificate of Analysis | Feb 07, 2025 | I137311 |
| E2305337 | Certificate of Analysis | Feb 07, 2025 | I137311 |
| E2305342 | Certificate of Analysis | Feb 07, 2025 | I137311 |
| E2305349 | Certificate of Analysis | Feb 07, 2025 | I137311 |
| E2305309 | Certificate of Analysis | Apr 13, 2023 | I137311 |
| B2318497 | Certificate of Analysis | Aug 03, 2021 | I137311 |
| L2219079 | Certificate of Analysis | Aug 03, 2021 | I137311 |
| Solubilidad | Soluble in water. |
|---|---|
| Sensibilidad | light sensitive;heat sensitive; air sensitive |
| Índice de refracción | 1.572 |
| Punto de inflamación (°F) | 149 °F |
| Punto de inflamación (°C) | 65°C(lit.) |
| Punto de ebullición (°C) | 85 °C/25 mmHg |
| Peso molecular | 171.960 g/mol |
| XLogP3 | 0.600 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 171.939 Da |
| Monoisotopic Mass | 171.939 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 4 |
| Formal Charge | 0 |
| Complexity | 10.000 |
| 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 |
| 1. Jianxiong Xu, Yuecong Luo, Yin Chen, Ziyu Guo, Yutong Zhang, Shaowen Xie, Na Li, Lijian Xu. (2022) Tough, Self-Recoverable, Spiropyran (SP3) Bearing Polymer Beads Incorporated PAM Hydrogels with Sole Mechanochromic Behavior. Gels, 8 (4): (208). [PMID:35448109] [10.3390/gels8040208] |
| 2. Fan Chuyao, Deng Qiang, Zhu Ting F.. (2021) Bioorthogonal information storage in l-DNA with a high-fidelity mirror-image Pfu DNA polymerase. NATURE BIOTECHNOLOGY, 39 (12): (1548-1555). [PMID:34326549] [10.1038/s41587-021-00969-6] |
| 3. Jia Tian, Chao Xiao, Baoxuan Huang, Chao Wang, Weian Zhang. (2019) Janus macromolecular brushes for synergistic cascade-amplified photodynamic therapy and enhanced chemotherapy. Acta Biomaterialia, [PMID:31726248] [10.1016/j.actbio.2019.11.018] |
| 4. Jia Tian, Chao Xiao, Baoxuan Huang, Xiaoze Jiang, Hongliang Cao, Feng Liu, Weian Zhang. (2019) Combating Multidrug Resistance through an NIR-Triggered Cyanine-Containing Amphiphilic Block Copolymer. ACS Applied Bio Materials, [PMID:35030676] [10.1021/acsabm.8b00793] |
| 5. Jinhao Yan, Haoqi Wang, Xueqin Zhao, Longxiang Tao, Xuefu Wang, Jun Yin. (2024) Polymorphic Supramolecular Therapeutic Platforms with Precise Dye/Drug Ratio to Perform Synergistic Chemo-Photo Anti-Tumor Therapy and Long-Term Immune Protection. Advanced Healthcare Materials, [PMID:39375970] [10.1002/adhm.202402907] |
| 6. Xu Zijie, Liu Xingyao, Yu Chongwen, Fan Xinyu, Yan Zhongwei, Xiao Haotian, Song Yujie, Xu Jian. (2025) Photochromic functionalization of polyetheramine-cured epoxy resin based on spiropyran derivatives doping. JOURNAL OF POLYMER RESEARCH, 32 (5): (1-14). [PMID:] [10.1007/s10965-025-04378-0] |
