2-Iodoethanol - ≥96%(GC), copper as stabilizer , CAS No.624-76-0

CAS: 624-76-0 Cat. No.: I575056 Molecular Weight: 171.97 Beilstein Registry Number: 1339 EC Number: 210-861-6

GRADE & PURITY ≥96%(GC), copper as stabilizer

Synonyms

AKOS005146198 | DTXSID3060792 | 2-IODOETHANOL | 2-iodo-ethanol | I0391 | InChI=1/C2H5IO/c3-1-2-4/h4H,1-2H | 2-Indoethanol | iodoethyl alcohol | STL560151 | 2-iodoethan-1-ol | A8634 | Ethanol, 2-iodo- | NSC85227 | NSC-85227 | BRN 1098258 | 2-hydroxyethyl i

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Synonyms

AKOS005146198 | DTXSID3060792 | 2-IODOETHANOL | 2-iodo-ethanol | I0391 | InChI=1/C2H5IO/c3-1-2-4/h4H, 1-2H | 2-Indoethanol | iodoethyl alcohol | STL560151 | 2-iodoethan-1-ol | A8634 | Ethanol, 2-iodo- | NSC85227 | NSC-85227 | BRN 1098258 | 2-hydroxyethyl i

Specifications & Purity

≥96%(GC), copper as stabilizer

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥96%(GC)

Names and Identifiers

• Pubchem Sid: 504752286
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752286
• Canonical Smiles: C(CI)O
• IUPAC Name: 2-iodoethanol
• InChIKey: QSECPQCFCWVBKM-UHFFFAOYSA-N
• INCHI: 1S/C2H5IO/c3-1-2-4/h4H,1-2H2
• Isomeric SMILES: C(CI)O
• WGK Germany: 3
• RTECS: KL3820000
• Molecular Weight: 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=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Class Halohydrins
      • Subclass Iodohydrins

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Class: 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
• Description: 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

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: Soluble in water.
• Sensitivity: Sensitive to light; Sensitive to heat; Sensitive to air
• Refractive Index: 1.572
• Flash Point(°F): 149 °F
• Flash Point(°C): 65°C(lit.)
• Boil Point(°C): 85 °C/25 mmHg
• Molecular Weight: 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

References

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]