Skip to Content
Merck
CN

250295

1,8-Diiodooctane

98%, contains copper as stabilizer

Synonym(s):

Octamethylene diiodide

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
I(CH2)8I
CAS Number:
Molecular Weight:
366.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
246-456-6
Beilstein/REAXYS Number:
1735437
MDL number:
Assay:
98%
Form:
liquid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

KZDTZHQLABJVLE-UHFFFAOYSA-N

InChI

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

SMILES string

ICCCCCCCCI

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.)

functional group

iodo

Quality Level

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

hcodes

Hazard Classifications

Aquatic Chronic 4

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
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
Ignasi Burgués-Ceballos et al.
ChemSusChem, 8(24), 4209-4215 (2015-12-15)
The application of conjugated materials in organic photovoltaics (OPVs) is usually demonstrated in lab-scale spin-coated devices that are processed under controlled inert conditions. Although this is a necessary step to prove high efficiency, testing of promising materials in air should

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service