2-Iodoethanol, 99%, stab. with copper
2-Iodoethanol, 99%, stab. with copper
2-Iodoethanol, 99%, stab. with copper
Thermo Scientific Chemicals

2-Iodoethanol, 99%, stab. with copper

CAS: 624-76-0 | C2H5IO | 171.97 g/mol
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Catalog number A14658.06
also known as A14658-06
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38.65
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Quantity:
5 g
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Price (USD)
38.65
Special offer
Online exclusive
Ends: 28-Dec-2026
45.10
Save 6.45
Each
Chemical Identifiers
CAS624-76-0
IUPAC Name2-iodoethan-1-ol
Molecular FormulaC2H5IO
InChI KeyQSECPQCFCWVBKM-UHFFFAOYSA-N
SMILESOCCI
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SpecificationsSpecification SheetSpecification Sheet
Identification (FTIR)Conforms
FormLiquid
Refractive Index1.5695-1.5735 @ 20?C
Appearance (Color)Clear colorless to yellow
Assay (GC)≥98.5%
2-Iodoethanol is used in the preparation of the neuroexcitants such as 4-dicarboxylic acid, alfa-kainic acid, 3-(carboxymethyl)pyrrolidine-2 and alfa-isokainic acid.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-Iodoethanol is used in the preparation of the neuroexcitants such as 4-dicarboxylic acid, alfa-kainic acid, 3-(carboxymethyl)pyrrolidine-2 and alfa-isokainic acid.

Solubility
Soluble in water.

Notes
Light sensitive. Store in a cool place. Incompatible with acid anhydrides, acid chlorides, phosphorus halides, strong acids, strong oxidizing agents and strong reducing agents.
RUO – Research Use Only

General References:

  1. Granchi, C.; Capecchi, A.; Del Frate, G.; Martinelli, A.; Macchia, M.; Minutolo, F.; Tuccinardi, T. Development and Validation of a Docking-Based Virtual Screening Platform for the Identification of New Lactate Dehydrogenase Inhibitors. Molecules 2015, 20 (5), 8772-8790.
  2. Abdel-Fattah, M. A. O.; Abadi, A. H.; Lehmann, J.; Schweikert, P. M.; Enzensperger, C. D1-like receptors distinguishing thieno-azecine regioisomers. Med. Chem. Commun. 2015, 6 (9), 1679-1686.