Basic information Safety Supplier Related

cis-1,4-Cyclohexanedicarboxybic acid

Basic information Safety Supplier Related

cis-1,4-Cyclohexanedicarboxybic acid Basic information

Product Name:
cis-1,4-Cyclohexanedicarboxybic acid
Synonyms:
  • 1,4-Cyclohexanedicarboxylic acid, cis-
  • CIS-HEXAHYDROTEREPHTHALIC ACID
  • CIS-1,4-CYCLOHEXANEDICARBOXYBIC ACID
  • CIS-1,4-CYCLOHEXANEDICARBOXYLIC ACID
  • Cyclohexanedicarboxylicacid
  • cis-Cyclohexane-1,4-dicarboxylic acid
  • cis-1,4-Cyclohexanedicarboxylic Acid >
  • Cis-1,4-CyclohexanedicarboxylicAci
CAS:
619-81-8
MF:
C8H12O4
MW:
172.18
EINECS:
999-999-2
Product Categories:
  • chiral
  • 4-Substituted Cyclohexanecarboxylic Acids
Mol File:
619-81-8.mol
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cis-1,4-Cyclohexanedicarboxybic acid Chemical Properties

Melting point:
168 °C
Boiling point:
384.1±35.0 °C(Predicted)
Density 
1.3200
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Ethanol,Ether,Chloroform,Methanol
form 
powder to crystal
pka
4.51±0.25(Predicted)
color 
White to Almost white
CAS DataBase Reference
619-81-8(CAS DataBase Reference)
NIST Chemistry Reference
cis-Hexahydroterephthalic acid(619-81-8)
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Safety Information

HS Code 
29172090
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cis-1,4-Cyclohexanedicarboxybic acid Usage And Synthesis

Definition

ChEBI: 1,4-cyclohexanedicarboxylic acid is a dicarboxylic acid that is cyclohexane substituted by carboxy groups at positions 1 and 4.

Synthesis

100-21-0

619-81-8

The general procedure for synthesizing cis-1,4-cyclohexanedicarboxylic acid from terephthalic acid was as follows: 200 g of terephthalic acid, 15 g of the Pd-Pt/C catalyst of Examples 1 to 14 and 1000 g of water were added to an autoclave, and stirring was initiated. The reaction system was first purged with nitrogen three times, followed by hydrogen replacement three times. The hydrogen pressure was adjusted to 4 MPa, the reaction temperature was maintained at 200°C, and hydrogen was continuously supplied under this condition for 3 hours. At the end of the reaction, the catalyst was removed by filtration while hot. The filtrate was cooled and filtered again to collect the filter cake. The filter cake was dried at 120°C to obtain the solid product. The solid product was analyzed by liquid chromatography to determine the contents of 1,4-cyclohexanedicarboxylic acid and trans-1,4-cyclohexanedicarboxylic acid therein, from which the yield of 1,4-cyclohexanedicarboxylic acid and the selectivity of trans-1,4-cyclohexanedicarboxylic acid were calculated, and the specific results are listed in Table 2.

References

[1] Patent: CN103769089, 2016, B. Location in patent: Paragraph 0029; 0030
[2] RSC Advances, 2017, vol. 7, # 30, p. 18178 - 18188
[3] Patent: CN105237341, 2016, A. Location in patent: Paragraph 0014
[4] Patent: KR2017/36493, 2017, A. Location in patent: Paragraph 0057; 0058; 0059
[5] Patent: KR2018/35585, 2018, A. Location in patent: Paragraph 0117-0121; 0145; 0146

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