≥98%(N) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Application：
Tetramethylsuccinonitrile can be used as a reactant to synthesize:
3,4-Dihydro-3H-pyrrol-2-imines by reacting with aryl lithium species in the presence of TMSCl.
Phenyl substituted metal-free fused tetraazachlorins by condensation reaction with substituted phthalonitrile derivatives in the presence of InCl3.
| Pubchem Sid | 504752904 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504752904 |
| Canonical Smiles | CC(C)(C#N)C(C)(C)C#N |
| IUPAC Name | 2,2,3,3-tetramethylbutanedinitrile |
| InChIKey | ZVQXQPNJHRNGID-UHFFFAOYSA-N |
| INCHI | 1S/C8H12N2/c1-7(2,5-9)8(3,4)6-10/h1-4H3 |
| Isomeric SMILES | CC(C)(C#N)C(C)(C)C#N |
| RTECS | WN4025000 |
| PubChem CID | 18745 |
| UN Number | 3439 |
| Packing Group | I |
| Molecular Weight | 136.2 |
| Beilstein | 2(4)2054 |
| Reaxy-Rn | 1752813 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →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 |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 L2214460 | Certificate of Analysis | Apr 02, 2026 | T161622 |
| L2214461 | Certificate of Analysis | Apr 02, 2026 | T161622 |
| L2214462 | Certificate of Analysis | Apr 02, 2026 | T161622 |
| L2214463 | Certificate of Analysis | Apr 02, 2026 | T161622 |
| F2015010 | Certificate of Analysis | Apr 02, 2024 | T161622 |
| L2214459 | Certificate of Analysis | Oct 24, 2022 | T161622 |
| Solubility | Insoluble in water; Soluble in Methanol,Ethanol |
|---|---|
| Melt Point(°C) | 171 °C |
| Molecular Weight | 136.190 g/mol |
| XLogP3 | 1.500 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 136.1 Da |
| Monoisotopic Mass | 136.1 Da |
| Topological Polar Surface Area | 47.600 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 192.000 |
| 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 |
