Skip to Content
Merck
All Photos(2)

Key Documents

932221

Sigma-Aldrich

1,4,5,8-Naphthalenetetracarboxylic dianhydride

≥98%

Synonym(s):

6,13-Dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),2,4(16),8,10-pentaene-5,7,12,14-tetrone, Isochromeno[6,5,4-def]isochromene-1,3,6,8-tetraone, NTDA, Naphthalene-1,4,5,8-tetracarboxylic dianhydride, NTCDA

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C14H4O6
CAS Number:
Molecular Weight:
268.18
Beilstein:
272788
MDL number:
UNSPSC Code:
12352005
NACRES:
NA.23

grade

sublimed grade

Quality Level

Assay

≥98 (elemental analysis)
≥98%

loss

0.5% TGA, > 270 °C (weight loss)

mp

>300 °C (lit.)

solubility

dichloromethane: soluble

fluorescence

λem 392 nm±10 nm in dichloromethane

λ

in dichloromethane

UV absorption

λ: 366 nm±5 nm Amax

SMILES string

O=C1OC(=O)c2ccc3C(=O)OC(=O)c4ccc1c2c34

InChI

1S/C14H4O6/c15-11-5-1-2-6-10-8(14(18)20-12(6)16)4-3-7(9(5)10)13(17)19-11/h1-4H

InChI key

YTVNOVQHSGMMOV-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

1,4,5,8-Naphthalenetetracarboxylic dianhydride, also known as NTCDA or NTCDA-DA, is commonly used as a building block or precursor for the synthesis of organic semiconducting materials. These materials can be employed in various organic electronic devices, including organic field-effect transistors (OFETs), organic photovoltaic (OPV) devices and organic photodetectors. NTCDA can be utilized as an electron-accepting material or an anchoring unit in studies on dye-sensitized solar cells (DSSCs) for enhancing the photovoltaic performance of the device.
1,4,5,8-Naphthalenetetracarboxylic dianhydride, also known as NTDA or NTCDA, is an organic compound related to naphthalene. NTDA is most commonly used as a precursor to naphthalenediimides (NDIs) (such as napthalenetetracarboxylic diimide), which has many uses, especially in energy harvesting and storage. NTCDA is used in electrode interface for organic photovoltaics, selective adsorption and to fabricate copolyimides to use in membranes for gas separation and for enhanced proton exchange membranes in fuel cells.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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’.

Already Own This Product?

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

Visit the Document Library

Chemically tethered functionalized graphene oxide based novel sulfonated polyimide composite for polymer electrolyte membrane
Rehman, W. et al.
Journal of Polymer Research, 26, 1-14 (2019)
Novel Sulfonated Co-poly(ether imide)s Containing Trifluoromethyl, Fluorenyl and Hydroxyl Groups for Enhanced Proton Exchange Membrane Properties: Application in Microbial Fuel Cell.
Kumar, A.G. et al.
ACS Applied Materials & Interfaces, 10, 14803-14817 (2018)
Reduction of Series Resistance in Organic Photovoltaic Cells Using a Metal-Doped Layer
Nakayama Ken-ichi, et al.
Japanese Journal of Applied Physics, 44, 633?635-633?635 (2005)
Linear and nonlinear optical properties of anhydride derivatives: A theoretical investigation
Bekki, Yahiaoui, et al.
Chemical Data Collections, 37, 100809-100809 (2022)
A Crystalline Polyimide Porous Organic Framework for Selective Adsorption of Acetylene over Ethylene
Jiang, L. et al.
Journal of the American Chemical Society, 140, 15724-15730 (2018)

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