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238295

Sigma-Aldrich

1-Iodooctane

98%

Synonym(s):

Octyl iodide

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About This Item

Linear Formula:
CH3(CH2)7I
CAS Number:
629-27-6
Molecular Weight:
240.13
Beilstein/REAXYS Number:
1697479
EC Number:
211-084-5
MDL number:
MFCD00001105
UNSPSC Code:
12352100
PubChem Substance ID:
24854155
NACRES:
NA.22

Quality Level

200

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.)

SMILES string

CCCCCCCCI

InChI

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

InChI key

UWLHSHAHTBJTBA-UHFFFAOYSA-N

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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
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

wgk_germany

WGK 3

flash_point_f

closed cup

flash_point_c

closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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’.

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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

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