1-Iodooctane, 98+%, stab. with copper, Thermo Scientific Chemicals
1-Iodooctane, 98+%, stab. with copper, Thermo Scientific Chemicals
Thermo Scientific Chemicals

1-Iodooctane, 98+%, stab. with copper, Thermo Scientific Chemicals

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Catalog number B22214.22
also known as B22214-22
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80.65
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100 g
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Price (USD)/ Each
80.65
Online exclusive
89.50 
Save 8.85 (10%)
Add to cart
1-Iodooctane, 98+%, stab. with copper, Thermo Scientific Chemicals
Catalog numberB22214.22
Price (USD)/ Each
80.65
Online exclusive
89.50 
Save 8.85 (10%)
-
Add to cart
Chemical Identifiers
CAS629-27-6
IUPAC Name1-iodooctane
Molecular FormulaC8H17I
InChI KeyUWLHSHAHTBJTBA-UHFFFAOYSA-N
SMILESCCCCCCCCI
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥98.0%
Identification (FTIR)Conforms
Refractive Index1.4865-1.4910 @ 20?C
FormLiquid
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Alkylation of [2,2?-([2,2?-bipyridine]-6,6?-diyl)bis[phenolato]-N,N?,O,O?]nickel(II)was performed using the catalytic reduction of 1-iodooctane. Primary alkyl iodide 1-iodooctane reacts with lithium aluminum deuteride (LAD) in a 1:0.2 ratio to form 1-deuteriooctane.

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
Alkylation of [2,2′-([2,2′-bipyridine]-6,6′-diyl)bis[phenolato]-N,N′,O,O′]nickel(II)was performed using the catalytic reduction of 1-iodooctane. Primary alkyl iodide 1-iodooctane reacts with lithium aluminum deuteride (LAD) in a 1:0.2 ratio to form 1-deuteriooctane.

Solubility
Insoluble in water.

Notes
Light Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, light, bases.
RUO – Research Use Only

General References:

  1. Raess PW, et al. J. 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. Electroanal. Chem. 2007, 603 (1), 124-34.
  2. Danielle M Goken,; Dennis G Peters,; Jonathan A Karty,; James P Reilly. Alkylation of [2,2'-([2,2'-bipyridine]-6,6'-diyl)bis[phenolato]-N,N',O,O']nickel(II) during catalytic reduction of 1-iodooctane. Journal of Electroanalytical Chemistry. 2004, 564 123-132.