Skip to Content
Merck
All Photos(1)

Documents

176850

Sigma-Aldrich

2-Iodoethanol

99%

Synonym(s):

2-Hydroxyethyl iodide, 2-Iodoethan-1-ol, Ethylene iodohydrin

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
ICH2CH2OH
CAS Number:
Molecular Weight:
171.97
Beilstein:
1098258
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.572 (lit.)

bp

85 °C/25 mmHg (lit.)

density

2.205 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

OCCI

InChI

1S/C2H5IO/c3-1-2-4/h4H,1-2H2

InChI key

QSECPQCFCWVBKM-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

The standard molar enthalpy of 2-iodoethanol formation has been studied.

Application

2-Iodoethanol was used in the synthesis of the neuroexcitants 3-(carboxymethyl)pyrrolidine-2,4-dicarboxylic acid, α-kainic acid, alpha-isokainic acid and alpha-dihydroallokainic acid.

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 2 Oral

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

149.0 °F - closed cup

Flash Point(C)

65 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

David M Hodgson et al.
The Journal of organic chemistry, 70(22), 8866-8876 (2005-10-22)
[reaction; see text] N-Boc syn-7-(2-hydroxyethyl)-4-(alkyl or aryl)sulfonyl-2-azabicyclo[2.2.1]hept-5-enes serve as precursors in syntheses of the neuroexcitants 3-(carboxymethyl)pyrrolidine-2,4-dicarboxylic acid 43, alpha-kainic acid 12, alpha-isokainic acid 14, and alpha-dihydroallokainic acid 77. The key step in these syntheses is the intermolecular radical addition of
Carlos E S Bernardes et al.
The journal of physical chemistry. A, 111(9), 1713-1720 (2007-02-10)
The energetics of the C-F, C-Cl, C-Br, and C-I bonds in 2-haloethanols was investigated by using a combination of experimental and theoretical methods. The standard molar enthalpies of formation of 2-chloro-, 2-bromo-, and 2-iodoethanol, at 298.15 K, were determined as
Abdullah M Alswieleh et al.
Designed monomers and polymers, 22(1), 226-235 (2019-12-20)
Poly(2‑(tert-butylamino)ethyl methacrylate) brushes (PTBAEMA) are grown from mesoporous silica nanoparticles via surface-initiated atom transfer radical polymerization (SI-ATRP). Linear PTBAEMA brushes are protonated and highly swollen at low pH; brushes are collapsed at pH higher than 7.7 due to deprotonation, as

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service