538035
1,4-Cyclohexanedicarboxylic acid
99%
Synonym(s):
1,4-CHDA-HP
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About This Item
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Quality Level
Assay
99%
mp
164-167 °C (lit.)
functional group
carboxylic acid
SMILES string
OC(=O)C1CCC(CC1)C(O)=O
InChI
1S/C8H12O4/c9-7(10)5-1-2-6(4-3-5)8(11)12/h5-6H,1-4H2,(H,9,10)(H,11,12)
InChI key
PXGZQGDTEZPERC-UHFFFAOYSA-N
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General description
1,4-Cyclohexanedicarboxylic acid (1,4-CHDA) has cyclohexane based structure. CHDA has better weatherability, higher impact strength, and faster stress relaxation. CHDA exhibits three isomeric forms:
- axial, axial (a,a) trans-isomer
- equatorial, equatorial (e,e) trans-isomer
- a,e cis-isomer
Application
1,4-Cyclohexanedicarboxylic acid may be used in the synthesis of:
- polyesters
- polyamides
- poly(butylene adipate-co-butylene 1,4-cyclohexanedicarboxylate) copolyester
- various polyester polyols
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis and characterization of transparent and high impact resistance polyurethane coatings based on polyester polyols and isocyanate trimers.
Progress in Organic Coatings, 75(4), 579-583 (2012)
Role of cis-1, 4-cyclohexanedicarboxylic acid in the regulation of the structure and properties of a poly (butylene adipate-co-butylene 1, 4-cyclohexanedicarboxylate) copolymer.
Royal Society of Chemistry Advances, 6(70), 65889-65897 (2016)
Advanced Polymerization and Properties of Biobased High T g polyester of Isosorbide and 1, 4-Cyclohexanedicarboxylic Acid through in Situ Acetylation.
Macromolecules, 46(8), 2930-2940 (2013)
Controlled stereochemistry of polyamides derived from cis/trans-1, 4-cyclohexanedicarboxylic acid.
Journal of Polymer Science Part A: Polymer Chemistry, 39(6), 833-840 (2001)
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