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176850

2-Iodoethanol

Name: 2-Iodoethanol
Brand: ALDRICH

99%

Synonym(s):

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

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About This Item

Linear Formula:

ICH₂CH₂OH

CAS Number:

624-76-0

Molecular Weight:

171.97

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24850603

EC Number:

210-861-6

Beilstein/REAXYS Number:

1098258

MDL number:

MFCD00002830

Assay:

99%

Form:

liquid

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Properties

Quality Level

100

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.)

functional group

hydroxyl, iodo

storage temp.

2-8°C

SMILES string

OCCI

InChI

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

InChI key

QSECPQCFCWVBKM-UHFFFAOYSA-N

Description

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

GHS06

signalword

Danger

hcodes

H300

pcodes

P264 - P270 - P301 + P310 - P405 - P501

Hazard Classifications

Acute Tox. 2 Oral

Storage Class

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

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Stereocontrolled syntheses of kainoid amino acids from 7-azabicyclo[2.2.1]heptadienes using tandem radical addition-homoallylic radical rearrangement.

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

Energetics of C-F, C-Cl, C-Br, and C-I bonds in 2-haloethanols. enthalpies of formation of XCH(2)CH(2)OH (X = F, Cl, Br, I) compounds and of the 2-hydroxyethyl radical.

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

Surface modification of pH-responsive poly(2-(tert-butylamino)ethyl methacrylate) brushes grafted on mesoporous silica nanoparticles.

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

Global Trade Item Number

SKU	GTIN
176850-5G	04061837632204
176850-25G	04061838753038