660477
3,4-Propylenedioxythiophene-2,5-dicarboxylic acid
97%
Synonym(s):
2,3-Dihydro-2H-thieno[3,4-b][1,4]dioxepin-6,8-dicarboxylic acid
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C9H8O6S
CAS Number:
Molecular Weight:
244.22
UNSPSC Code:
12352103
PubChem Substance ID:
MDL number:
InChI
1S/C9H8O6S/c10-8(11)6-4-5(7(16-6)9(12)13)15-3-1-2-14-4/h1-3H2,(H,10,11)(H,12,13)
SMILES string
OC(=O)c1sc(C(O)=O)c2OCCCOc12
InChI key
MCLQXEPXGNPDHG-UHFFFAOYSA-N
assay
97%
form
solid
mp
>250 °C (dec.)
General description
3,4-Propylenedioxythiophene-2,5-dicarboxylic acid (ProDOT) is an electron rich conducting polymer that can be used in organic and bio-electronics. It can functionalize a variety of polymers by enhancing the intrinsic properties.
Application
ProDOT is a conjugating polymer that can be used in the fabrication of a variety of organic electronics which include electrochromic devices, lithium ion batteries, and organic semiconductors.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Conducting poly (3, 4-alkylenedioxythiophene) derivatives as fast electrochromics with high-contrast ratios.
Kumar A, et al.
Chemistry of Materials, 10(3), 896-902 (1998)
Propylenedioxythiophene (ProDOT)-phenylene copolymers allow a yellow-to-transmissive electrochrome.
Amb CM, et al.
Polym. Chem., 2(4), 812-814 (2011)
Easy-to-make carboxylic acid dioxythiophene monomer (ProDOT-COOH) and functional conductive polymers.
Mantione D, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 55(17), 2721-2724 (2017)
3, 4-Alkylenedioxy ring formation via double Mitsunobu reactions: an efficient route for the synthesis of 3, 4-ethylenedioxythiophene (EDOT) and 3, 4-propylenedioxythiophene (ProDOT) derivatives as monomers for electron-rich conducting polymers.
Zong K, et al.
Chemical Communications (Cambridge, England), 2498-2499 (2002)
Multifunctional SA-PProDOT binder for lithium ion batteries.
Ling M, et al.
Nano Letters, 15(7), 4440-4447 (2015)
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