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electronic grade, ≥99% metals basis Electronic grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Description
Monomer used in the preparation of polyimide coatings for electronic applications-IC passivation, dielectric for multichip modules, and as a stress relief layer in sensor applications.
| Sonrisas canónicas | CC1=C(C(=C(C(=C1N)C)C)N)C |
|---|---|
| IUPAC Name | 2,3,5,6-tetramethylbenzene-1,4-diamine |
| InChIKey | WCZNKVPCIFMXEQ-UHFFFAOYSA-N |
| INCHI | 1S/C10H16N2/c1-5-6(2)10(12)8(4)7(3)9(5)11/h11-12H2,1-4H3 |
| Isómeros SMILES | CC1=C(C(=C(C(=C1N)C)C)N)C |
| RTECS | CZ1599700 |
| PubChem CID | 76548 |
| Peso molecular | 164.25 |
| Beilstein | 13(4)313 |
| Reaxy-Rn | 2208743 |
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 | Benzenoids |
| Clase | Benzene and substituted derivatives |
| Subclass | Aniline and substituted anilines |
| Intermediate Tree Nodes | Phenylenediamines |
| Direct Parent | P-phenylenediamines |
| Alternative Parents | Primary amines Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | P-phenylenediamine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as p-phenylenediamines. These are aromatic compound containing a benzene ring which carries 2 amino groups, at the 1- and 4-positions. |
| External Descriptors | Not available |
| Punto de fusión (°C) | 152℃ |
|---|---|
| Peso molecular | 164.250 g/mol |
| XLogP3 | 2.000 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 164.131 Da |
| Monoisotopic Mass | 164.131 Da |
| Topological Polar Surface Area | 52.000 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 124.000 |
| 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 |
| 1. Ke Chen, Linhan Ni, Hao Zhang, Jia Xie, Xin Yan, Saisai Chen, Junwen Qi, Chaohai Wang, Xiuyun Sun, Jiansheng Li. (2021) Veiled metal organic frameworks nanofillers for mixed matrix membranes with enhanced CO2/CH4 separation performance. SEPARATION AND PURIFICATION TECHNOLOGY, [PMID:] [10.1016/j.seppur.2021.119707] |
| 2. Lingyu Liu, Qixuan Li, Luxin Sun, Aqib Riaz, Jianxin Li, Yingge Wang, Ingo Pinnau, Xiaohua Ma. (2024) Ultrahigh He enrichment property of carbon molecular sieve membranes by direct fluorination. JOURNAL OF MEMBRANE SCIENCE, [PMID:] [10.1016/j.memsci.2024.123647] |
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