Isophorone diamine

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Isophorone diamine
Isophorone diamine.svg
Names
IUPAC name
3-(Aminomethyl)-3,5,5-trimethylcyclohexan-1-amine
Other names
Isophorondiamin; IPDA
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.018.788 Edit this at Wikidata
EC Number
  • 220-666-8
UNII
UN number 2289
  • InChI=1S/C10H22N2/c1-9(2)4-8(12)5-10(3,6-9)7-11/h8H,4-7,11-12H2,1-3H3
    Key: RNLHGQLZWXBQNY-UHFFFAOYSA-N
  • CC1(CC(CC(C1)(C)CN)N)C
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
1.4880
Hazards
GHS labelling:
GHS05: CorrosiveGHS07: Exclamation mark
Signal word
 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).
Infobox references

Isophorone diamine (usually shortened to IPDA) is a diamine with the formula (CH3)3C6H7(NH2)(CH2NH2). It is a colorless liquid. It is a precursor to polymers and coatings.[1]

Production[]

It 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[]

IPDA 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 (engineering) 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.

See also[]

References[]

  1. ^ a b Hardo Siegel, Manfred Eggersdorfer (2005). "Ketones". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a15_077.CS1 maint: uses authors parameter (link)
  2. ^ The polyurethanes book. Randall, David, Lee, Steve, 1941-. [Everberg, Belgium]: [Huntsman Polyurethanes]. 2002. ISBN 0470850418. OCLC 50479333.CS1 maint: others (link)
  3. ^ Pilato, Louis A.; Michno, Michael J. (1994-11-04). Advanced Composite Materials. Springer Science & Business Media. ISBN 9783540575634.
  4. ^ "Cycloaliphatic Amines - Hexion.com". www.hexion.com. Retrieved 2018-08-17.
  5. ^ "A New Epoxy Curing Agent with Long Pot Life and Fast Cure". www.pcimag.com. Retrieved 2021-05-18.

External links[]

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