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251178

Sigma-Aldrich

1,6-Diiodohexane

97%, contains copper as stabilizer

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About This Item

Linear Formula:
I(CH2)6I
CAS Number:
629-09-4
Molecular Weight:
337.97
EC Number:
211-073-5
MDL number:
MFCD00001103
UNSPSC Code:
12352100
PubChem Substance ID:
24855114
NACRES:
NA.22

Quality Level

100

Assay

97%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.5852 (lit.)

bp

141-142 °C/10 mmHg (lit.)

mp

9-10 °C (lit.)

density

2.05 g/mL at 25 °C (lit.)

SMILES string

ICCCCCCI

InChI

1S/C6H12I2/c7-5-3-1-2-4-6-8/h1-6H2

InChI key

QLIMAARBRDAYGQ-UHFFFAOYSA-N

Related Categories

Application

1,6-Diiodohexane has been used:
  • in preparation of cationic tissue plasminogen activator (t-PA)-containing polyurethane surfaces
  • as solvent additive, to improve the power conversion effciency of polymer/fullerene bulk heterojunction solar cells
  • synthesis of new macrocycles, having 2,4-dihydroxybenzophenone as a connecting unit
  • preparation of a novel ionic electrolyte, 3-(iodohexyl)-1-(3-(triethoxysilyl)propylcarbamoyl)-1H-benzo[d]imidazol-3-ium iodide

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315 - H319 - H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °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’.

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Synthesis and structure of new cyclophanes containing benzofuran and benzene rings.
Park KK, et al.
Tetrahedron Letters, 41(9), 1393-1396 (2000)
Zhaoqiang Wu et al.
Acta biomaterialia, 7(5), 1993-1998 (2011-01-25)
With the aim of minimizing thrombus formation in blood-contacting devices, tissue plasminogen activator (t-PA)-containing polyurethane (PU) materials have been developed. Cationic PU surfaces were prepared by grafting poly(dimethylaminoethyl methacrylate) and quaternizing the tertiary amino groups with iodomethane or 1,6-diiodohexane or
Novel silane-substituted benzimidazolium iodide as gel electrolyte for dye-sensitized solar cells.
Lee JP, et al.
Electrochimica Acta, 54(18), 4635-4670 (2009)
Improving device efficiency of polymer/fullerene bulk heterojunction solar cells through enhanced crystallinity and reduced grain boundaries induced by solvent additives.
Ming-Shin Su et al.
Advanced materials (Deerfield Beach, Fla.), 23(29), 3315-3319 (2011-06-15)

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