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Merck
CN

250295

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24855049
EC Number:
246-456-6
Beilstein/REAXYS Number:
1735437
MDL number:
MFCD00001106

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Product Name

1,8-Diiodooctane, 98%, contains copper as stabilizer

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

200

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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

hcodes

H413

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

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Certificates of Analysis (COA)

Lot/Batch Number
0000384895
0000384341
0000333140
0000333140
0000384341

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Wei Song et al.
Chemistry, an Asian journal, 14(9), 1472-1476 (2019-02-26)
Development of low-cost water-/alcohol-soluble interfacial materials is a crucial issue to promote the commercialization of polymer solar cells (PSCs). Herein, two derivatives of low-cost rhodamine, called sulforhodamine 101 (SR101) and sulforhodamine B (SRB), are applied as cathode interfacial layers (CILs)
Jiali Song et al.
Advanced science (Weinheim, Baden-Wurttemberg, Germany), 7(18), 2001986-2001986 (2020-10-02)
Morphological stability is crucially important for the long-term stability of polymer solar cells (PSCs). Many high-efficiency PSCs suffer from metastable morphology, resulting in severe device degradation. Here, a series of copolymers is developed by manipulating the content of chlorinated benzodithiophene-4,8-dione
Zhi Jiang et al.
Proceedings of the National Academy of Sciences of the United States of America, 117(12), 6391-6397 (2020-03-11)
Flexible organic photovoltaics (OPVs) are promising power sources for wearable electronics. However, it is challenging to simultaneously achieve high efficiency as well as good stability under various stresses. Herein, we demonstrate the fabrication of highly efficient (efficiency, 13.2%) and stable
Lichun Chang et al.
Nanomaterials (Basel, Switzerland), 10(9) (2020-09-10)
Semi-transparent organic solar cells (ST-OSCs) have attracted significant research attention, as they have strong potential to be applied in automobiles and buildings. For ST-OSCs, the transparent top electrode is an indispensable component, where the dielectric/metal/dielectric (D/M/D) structured electrode displayed a
Soo Won Heo
Nanomaterials (Basel, Switzerland), 10(11) (2020-11-06)
In this study, we developed a method for fabricating ultrathin polymer substrates that can be used in ultra-flexible organic photovoltaics (OPVs) via a non-vacuum process using cyclic transparent optical polymer. In addition, a Ag nanowire network layer was used as
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