Isophorone diamine (usually shortened to IPDA) is a chemical compound and specifically a diamine with the formula (CH3)3C6H7(NH2)(CH2NH2). It is a colorless liquid. It is a precursor to polymers and coatings.[1]
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| Names | |
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| IUPAC name
3-(Aminomethyl)-3,5,5-trimethylcyclohexan-1-amine
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| Other names
Isophorondiamine; IPDA
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| Identifiers | |
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3D model (JSmol)
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.018.788 |
| EC Number |
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PubChem CID
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| UNII | |
| UN number | 2289 |
CompTox Dashboard (EPA)
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| Properties | |
| C10H22N2 | |
| Molar mass | 170.300 g·mol−1 |
| Appearance | Colourless liquid |
| Density | 0.922 |
| Melting point | 10 °C (50 °F; 283 K) |
| Boiling point | 247 °C (477 °F; 520 K) |
| Very good | |
Refractive index (nD)
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1.4880 |
| Hazards | |
| GHS labelling: | |
 
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| Danger | |
| H302, H312, H314, H317, H412 | |
| P260, P261, P264, P270, P272, P273, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P333+P313, P363, P405, P501 | |
| Flash point | 117°C |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Production
editIt is usually produced as a mixture of the cis- and trans-isomers. It is produced by hydrocyanation of isophorone followed by reductive amination and hydrogenation of the nitrile.[1]
Uses
editIPDA is used as a precursor in the manufacture of isophorone diisocyanate by phosgenation.[2]
Like other diamines or amines in general, it is a curing agent for epoxy resins. When used in coatings applications the higher cost compared to other amines is justified by the enhanced UV stability and thus lower yellowing tendency. In the production of advanced composite materials, its higher cost compared to other amines is less critical as performance is the key criteria.[3][4] Cycloaliphatic amines such as IPDA also are known to have lower yellowing tendency than other amines and are thus used in coatings applications where this feature is important for aesthetics. Although it is not the only cycloaliphatic amine used in epoxy flooring, it has the largest use by volume.[5] Other cycloaliphatic amines used in flooring include 1,3-BAC, MXDA, PACM and DCH-99.
In laboratory tests, Tokyo Metropolitan University found that IPDA was able to remove more than 99 percent of CO2 from air with a concentration of 400 parts per million (ppm) – about the level currently in the atmosphere. This process also happened much faster than other carbon capture techniques, removing 201 millimoles of CO2 per hour, per mole of the compound. That is at least twice as fast as other Direct Air Capture lab systems, and far faster than the leading artificial leaf device.
The pollutant separated out into flakes of a solid carbamic acid material, which could be removed from the liquid relatively easily. If need be, it can be converted back into gaseous CO2 by heating it to 60 °C (140 °F), which also releases the original liquid IPDA ready for reuse. Whether the carbon is kept as a solid or a gas, it can then be stored or reused in industrial or chemical processes. The research was published in the journal ACS Environmental Au.[6]
See also
editReferences
edit- ^ a b Siegel, Hardo; Eggersdorfer, Manfred (2005). "Ketones". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a15_077. ISBN 9783527306732.
- ^ Randall, David; Lee, Steve (2002). The polyurethanes book. [Everberg, Belgium]: [Huntsman Polyurethanes]. ISBN 0470850418. OCLC 50479333.
- ^ Pilato, Louis A.; Michno, Michael J. (1994-11-04). Advanced Composite Materials. Springer Science & Business Media. ISBN 9783540575634.
- ^ "Cycloaliphatic Amines - Hexion.com". www.hexion.com. Retrieved 2018-08-17.
- ^ "A New Epoxy Curing Agent with Long Pot Life and Fast Cure". www.pcimag.com. Retrieved 2021-05-18.
- ^ Kikkawa, Soichi; Amamoto, Kazushi; Fujiki, Yu; Hirayama, Jun; Kato, Gen; Miura, Hiroki; Shishido, Tetsuya; Yamazoe, Seiji (2022-05-10). "Direct Air Capture of CO 2 Using a Liquid Amine–Solid Carbamic Acid Phase-Separation System Using Diamines Bearing an Aminocyclohexyl Group". ACS Environmental Au. 2 (4): 354–362. doi:10.1021/acsenvironau.1c00065. ISSN 2694-2518. PMC 10125313. S2CID 248703204.