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Sigma-Aldrich

1,4-Diethynylbenzene

96%

Synonym(s):

1,4-Bis(ethynyl)benzene, 1,4-Diacetylenebenzene, 1,4-Diacetylenylbenzene, 1,4-Diethynylbenzene, p-Diethynylbenzene

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About This Item

Linear Formula:
HC≡CC6H4C≡CH
CAS Number:
Molecular Weight:
126.15
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

96%

form

solid

mp

94-98 °C (lit.)

storage temp.

2-8°C

SMILES string

C#Cc1ccc(cc1)C#C

InChI

1S/C10H6/c1-3-9-5-7-10(4-2)8-6-9/h1-2,5-8H

InChI key

MVLGANVFCMOJHR-UHFFFAOYSA-N

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Application

  • Advanced Sensor Development: A novel approach to creating sensitive and selective copper(II) sensors on carbon fiber microelectrodes using 1,4-Diethynylbenzene. This research enhances the performance and application range of electrochemical sensors, particularly in environmental monitoring and industrial processes (Nudurupati et al., 2023).
  • High-Performance OLED Materials: Synthesis of highly phosphorescent dimers of PtAu(2) complexes using 1,4-Diethynylbenzene. This research opens new pathways for creating more efficient and durable organic light-emitting diodes (OLEDs), which are crucial for the development of next-generation display and lighting technologies (Zheng et al., 2022).
  • Mixed-Valence Metal Complexes: A comprehensive study on the electronic structure and mixed-valence characteristics of 1,4-diethynylbenzene-bridged bimetallic complexes. This research provides insights into the tuning of electronic properties for potential applications in molecular electronics and catalysis (Safari et al., 2020).

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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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Hongyu Mi et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 176, 168-173 (2017-01-17)
In this work, a turn on fluorescent sensor, based on Hg
Tan L H Doan et al.
Chemistry, an Asian journal, 10(12), 2660-2668 (2015-08-11)
New Zr(IV)- and Hf(IV)-based metal-organic framework photocatalysts, termed VNU-1 and VNU-2 (where VNU = Vietnam National University), were synthesized and their resulting structures fully characterized. By employing a highly π-conjugated linker, namely 1,4-bis(2-[4-carboxyphenyl]ethynyl)benzene, the optical absorption properties were effectively red-shifted
Mingming Guan et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 35(6), 625-630 (2019-02-05)
A novel "on-off-on" super-sensitive conjugated polymer fluorescence sensor (PPE-DPA) was developed and it was applied to realize the continuous recognition of Cu2+ and pyrophosphate (PPi). The fluorescence intensity decreased linearly with the change of Cu2+ from 0.05 to 5.0 μmol
Reetendra Singh et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 20(13), 1728-1737 (2019-05-09)
Covalently cross-linked heterostructures of 2D materials are a new class of materials which possess electrochemical and photochemical hydrogen evolution properties. It was of considerable interest to investigate the role of interlayer spacing in the nanocomposites involving MoS2 and graphene sheets
Shasha Wang et al.
Scientific reports, 7(1), 12712-12712 (2017-10-07)
We developed an efficient one-pot metal-free click polymerization procedure for the synthesis of 3,5-disubstituted polypyrazoles with high yields, high molecular weights, and narrow molecular weight distribution. The method involved two click reactions in a one-pot synthesis. The first reaction was

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