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118184

Sigma-Aldrich

5-Amino-1,3,3-trimethylcyclohexanemethylamine, mixture of cis and trans

≥99%

Synonym(s):

Isophorone diamine

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About This Item

Linear Formula:
H2NC6H7(CH3)3CH2NH2
CAS Number:
2855-13-2
Molecular Weight:
170.30
EC Number:
220-666-8
MDL number:
MFCD00019397
UNSPSC Code:
12162002
PubChem Substance ID:
24847362
NACRES:
NA.23

Assay

≥99%

refractive index

n20/D 1.488 (lit.)

bp

247 °C (lit.)

mp

10 °C (lit.)

density

0.922 g/mL at 25 °C (lit.)

SMILES string

CC1(C)CC(N)CC(C)(CN)C1

InChI

1S/C10H22N2/c1-9(2)4-8(12)5-10(3,6-9)7-11/h8H,4-7,11-12H2,1-3H3

InChI key

RNLHGQLZWXBQNY-UHFFFAOYSA-N

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General description

5-Amino-1,3,3-trimethylcyclohexanemethylamine, mixture of cis and trans (IPD), is an cyclo-aliphatic diamine that is mainly used as an epoxy curing agent.

Application

IPD is widely used as a hardener to cure a variety of epoxy based resins, such as diglycidyl ether bisphenol A (DGEBA), and diglycidyl ether 1,4-butanediol (DGEBU)..

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H314,H317

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1A

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Contact sensitization due to isophoronediamine.
L Guerra et al.
Contact dermatitis, 27(1), 52-53 (1992-07-01)
Effect of dendrimer-functionalized magnetic iron oxide nanoparticles on improving thermal and mechanical properties of DGEBA/IPD epoxy networks
Jafari-Soghieh F, et al.
High Performance Polymers, 10(4), 0954008317749020-0954008317749020 (2017)
Syringaresinol: A Renewable and Safer Alternative to Bisphenol A for Epoxy-Amine Resins
Janvier M, et al.
ChemSusChem, 10(4), 738-746 (2017)
Carola Esposito Corcione et al.
Waste management (New York, N.Y.), 109, 212-221 (2020-05-16)
This paper reports the preparation of newly synthesized bio-epoxy monomers, suitable for replacing petrochemical-derived epoxy resins. An original green method able to produce epoxy monomers starting from neat carbohydrates, waste flours, and even from the organic fraction of municipal solid
Durability of adhesives based on different epoxy/aliphatic amine networks
Garcia F, et al.
International Journal of Adhesion and Adhesives, 31(4), 177-181 (2011)
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