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Tetracyanoethylene - 98%, high purity , CAS No.670-54-2

    Grade & Purity:
  • ≥98%
In stock
Item Number
T279033
Grouped product items
SKU Size
Availability
Price Qty
T279033-200mg
200mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$13.90
T279033-1g
1g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$52.90
T279033-5g
5g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$153.90
T279033-25g
25g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$641.90
T279033-100g
100g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$1,749.90
View related series
Nitriles (39)

Basic Description

Synonyms J-200117 | TCNE | Tetrakyanethylen [Czech] | AI3-28756 | delta(sup 2,2')-Bimalononitrile | 1,1,2,2-ethenetetracarbonitrile | 1,1,2,2-Ethylenetetracarbonitrile # | BBL027360 | EINECS 211-578-0 | Percyanoethylene | Tetracyanoethylene, 98% | Tox21_202940 | E
Specifications & Purity ≥98%
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Used for postfunctional addition to polyphenylacetylene derivatives to change the oxygen permeability. Reactant for: Regioselective [2+2] cycloaddition reaction for production of BODIPY dyes and TCBD derivatives Thermal addition reaction with alkynes One-pot reactions with nucleophilic reagents forming aromatic cyanovinyl compounds Synthesis of cobalt tetracyanoethylene films Biotransformation by Botrytis cinerea

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic nitrogen compounds
Class Organonitrogen compounds
Subclass Organic cyanides
Intermediate Tree Nodes Not available
Direct Parent Nitriles
Alternative Parents Organopnictogen compounds  Hydrocarbon derivatives  
Molecular Framework Aliphatic acyclic compounds
Substituents Nitrile - Carbonitrile - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as nitriles. These are compounds having the structure RC#N; thus C-substituted derivatives of hydrocyanic acid, HC#N.
External Descriptors Not available

Names and Identifiers

IUPAC Name ethene-1,1,2,2-tetracarbonitrile
INCHI InChI=1S/C6N4/c7-1-5(2-8)6(3-9)4-10
InChIKey NLDYACGHTUPAQU-UHFFFAOYSA-N
Smiles C(#N)C(=C(C#N)C#N)C#N
Isomeric SMILES C(#N)C(=C(C#N)C#N)C#N
WGK Germany 3
RTECS KM7300000
UN Number 2811
Molecular Weight 128.09
Beilstein 1679885
Reaxy-Rn 506867

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot Number Certificate Type Date Item
F2505095 Certificate of Analysis Jun 07, 2025 T279033
F2505096 Certificate of Analysis Jun 07, 2025 T279033
H2406580 Certificate of Analysis Mar 23, 2024 T279033
H2406581 Certificate of Analysis Mar 23, 2024 T279033
K2112587 Certificate of Analysis Aug 04, 2023 T279033
A2305756 Certificate of Analysis Nov 24, 2022 T279033
A2305763 Certificate of Analysis Nov 24, 2022 T279033
A2305757 Certificate of Analysis Nov 24, 2022 T279033
A2305679 Certificate of Analysis Nov 24, 2022 T279033

Chemical and Physical Properties

Solubility Soluble in methanol, benzene, toluene, water (hydrolyses to form HCN), and ether (slightly).,
Sensitivity Light and Moisture sensitive
Boil Point(°C) 223°C
Melt Point(°C) 198°C
Molecular Weight 128.090 g/mol
XLogP3 -0.200
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 0
Exact Mass 128.012 Da
Monoisotopic Mass 128.012 Da
Topological Polar Surface Area 95.200 Ų
Heavy Atom Count 10
Formal Charge 0
Complexity 289.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Alternative Products

Citations of This Product

1. Cao Jianfei, Yin Zuodong, Pang Qi, Lu Yuexi, Nong Xiuqing, Zhang Jin Zhong.  (2021)  Modulating optical properties and interfacial electron transfer of CsPbBr3 perovskite nanocrystals via indium ion and chlorine ion co-doping.  JOURNAL OF CHEMICAL PHYSICS,  155  (23):  
2. Xiu Chen, Ying Zhang, Jin Han, Linzhou Zhang, Suoqi Zhao, Chunming Xu, Quan Shi.  (2021)  Direct Nickel Petroporphyrin Analysis through Electrochemical Oxidation in Electrospray Ionization Ultrahigh-Resolution Mass Spectrometry.  ENERGY & FUELS,  35  (7): (5748–5757). 
3. Guohua Jiang, Tengteng Jiang, Xia Li, Zheng Wei, Xiangxiang Du, Xiaohong Wang.  (2014)  Boronic acid functionalized N-doped carbon quantum dots as fluorescent probe for selective and sensitive glucose determination.  Materials Research Express,  (2): (25708). 
4. Jinghang Li, Qi Shi, Chaoyu Song, Chenxi Shi, Yuguang Lv.  (2025)  Analysis of Tetracycline Modification Based on g-C3N4 Photocatalytic Degradation.  Inorganics,  13  (3): (77). 

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