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Sigma-Aldrich

1,8-Diiodooctane

98%, contains copper as stabilizer

Synonym(s):

Octamethylene diiodide

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About This Item

Linear Formula:
I(CH2)8I
CAS Number:
24772-63-2
Molecular Weight:
366.02
Beilstein:
1735437
EC Number:
246-456-6
MDL number:
MFCD00001106
UNSPSC Code:
12352100
PubChem Substance ID:
24855049
NACRES:
NA.22

Assay

98%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.5653 (lit.)

bp

167-169 °C/6 mmHg (lit.)

density

1.84 g/mL at 25 °C (lit.)

SMILES string

ICCCCCCCCI

InChI

1S/C8H16I2/c9-7-5-3-1-2-4-6-8-10/h1-8H2

InChI key

KZDTZHQLABJVLE-UHFFFAOYSA-N

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Application

1,8-Diiodooctane has been employed as processing additive:
  • to improve the morphology and the efficiency of bulk heterojunctions solar cells, based on the regioregular poly(3-hexylthiophene) and a soluble fullerene derivative
  • to improve the power conversion efficiency of polymer solar cells

Hazard Statements

H413

Precautionary Statements

P273 - P501

Hazard Classifications

Aquatic Chronic 4

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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Wang Li et al.
ACS applied materials & interfaces, 9(32), 27083-27089 (2017-07-27)
The development of simple and water-/alcohol-soluble interfacial materials is crucial for the cost-effective fabrication process of polymer solar cells (PSCs). Herein, highly efficient PSCs are reported employing water-/alcohol-soluble and low-cost rhodamines as cathode interfacial layers (CILs). The results reveal that
Chengkai Xia et al.
Polymers, 12(8) (2020-08-14)
In this study, a solution-processable compact vanadium oxide (V2O5) film with a globular nanoparticulate structure is introduced to the hole transport layer (HTL) of polymer bulk-heterojunction based solar cells comprised of PTB7:PC70BM by using a facile metal-organic decomposition method to
Zelin Li et al.
Small (Weinheim an der Bergstrasse, Germany), 14(16), e1704491-e1704491 (2018-03-24)
In recent years, rapid advances are achieved in polymer solar cells (PSCs) using nonfullerene small molecular acceptors. However, no research disclosing the influence of molecular weight (Mn ) of conjugated polymer on the nonfullerene device performance is reported. In this
Qian Liu et al.
ACS applied materials & interfaces, 6(3), 1601-1607 (2014-01-24)
9-Arylidene-9H-fluorene containing donor-acceptor (D-A) alternating polymers P1 and P2 were synthsized and used for the fabrication of polymer solar cells (PSCs). High and low molecular weight P1 (HMW-P1 and LMW-P1) and high molecular weight P2 were prepared to study the
Xing Fan et al.
Journal of nanoscience and nanotechnology, 14(5), 3592-3596 (2014-04-17)
Controlling the blend morphology is critical for achieving high power conversion efficiency in polymer/fullerene bulk heterojunction (BHJ) photovoltaic devices. As a simple and effective method to control morphology, adding processing additives has been widely applied in the organic BHJ solar
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