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Merck
CN

238295

1-Iodooctane

98%

Synonym(s):

Octyl iodide

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About This Item

Linear Formula:
CH3(CH2)7I
CAS Number:
Molecular Weight:
240.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-084-5
Beilstein/REAXYS Number:
1697479
MDL number:
Assay:
98%
Form:
liquid
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Quality Level

assay

98%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.4878 (lit.)

bp

225-226 °C (lit.)

mp

−46-−45 °C (lit.)

density

1.33 g/mL at 25 °C (lit.)

functional group

alkyl halide, iodo

SMILES string

CCCCCCCCI

InChI

1S/C8H17I/c1-2-3-4-5-6-7-8-9/h2-8H2,1H3

InChI key

UWLHSHAHTBJTBA-UHFFFAOYSA-N

General description

1-Iodooctane undergoes catalytic reduction by nickel (I) salen electrogenerated at a glassy carbon cathode in dimethylformamide. Radical mechanism of formation of monolayer on silicon ground in the presence of 1-iodooctane has been studied by X-ray photoelectron spectroscopy.


pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

188.6 °F - closed cup

flash_point_c

87 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Evidence for a radical mechanism in monolayer formation on silicon ground (or scribed) in the presence of alkyl halides.
Jiang G, et al.
Langmuir, 20(5), 17772-17774 (2004)
Catalytic reduction of 1-iodooctane by nickel (I) salen electrogenerated at carbon cathodes in dimethylformamide: Effects of added proton donors and a mechanism involving both metal-and ligand-centered one-electron reduction of nickel (II) salen.
Raess PW, et al.
Journal of Electroanalytical Chemistry, 603(1), 124-134 (2007)
Robert Löwe et al.
Molecules (Basel, Switzerland), 24(2) (2019-01-20)
Eight new polymerizable ammonium-TFSI ionic liquids were synthesized and characterized with respect to an application in energy storage devices. The ionic liquids feature methacrylate or acrylate termination as polymerizable groups. The preparation was optimized to obtain the precursors and ionic



Global Trade Item Number

SKUGTIN
238295-100G04061838786814
238295-25G04061837071690