ChemicalBook--->CAS DataBase List--->53611-01-1

53611-01-1

53611-01-1 Structure

53611-01-1 Structure
IdentificationBack Directory
[Name]

Hydrogenated trimellitic anhydride
[CAS]

53611-01-1
[Synonyms]

H-TMAn
H-TMAn-s
Hydrogeted trimellitic anhydride
Hydrogenated trimellitic anhydride
4-Carboxyhexahydrophthalic anhydride
1,2,4-Cyclohexanetricarboxylic anhydride
Cyclohexane-1,2,4-tricarboxylic acid anhydride
1,3-Dioxooctahydroisobenzofuran-5-carboxylic acid
1,2,4-cyclohexanetricarboxylic acid-1,2-anhydride
octahydro-1,3-dioxo-5-Isobenzofurancarboxylic acid
Cyclohexane-1,3,4-tricarboxylic acid 3,4-anhydride
cyclohexane-1,2,4-tricarboxylic acid-1,2-anhydride
5-Isobenzofurancarboxylic acid, octahydro-1,3-dioxo-
1,2,4-CYCLOHEXANETRICARBOXYLIC ANHYDRIDE (H-TMA)(CAS NO.53611-01-1)
[Molecular Formula]

C9H10O5
[MDL Number]

MFCD20640480
[MOL File]

53611-01-1.mol
[Molecular Weight]

198.17
Chemical PropertiesBack Directory
[Boiling point ]

449.4±45.0 °C(Predicted)
[density ]

1.446
[pka]

4.31±0.20(Predicted)
[InChI]

InChI=1S/C9H10O5/c10-7(11)4-1-2-5-6(3-4)9(13)14-8(5)12/h4-6H,1-3H2,(H,10,11)
[InChIKey]

FWHUTKPMCKSUCV-UHFFFAOYSA-N
[SMILES]

C1(=O)C2C(CC(C(O)=O)CC2)C(=O)O1
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)
GHS05
[Signal word ]

Danger
[Hazard statements ]

H318-H317-H315
[Precautionary statements ]

P280-P305+P351+P338-P310-P264-P280-P302+P352-P321-P332+P313-P362-P261-P272-P280-P302+P352-P333+P313-P321-P363-P501
Hazard InformationBack Directory
[Chemical Properties]

Colorless
[Synthesis]

The mixture of 60g of trimellitic anhydride, 120g of anhydrous acetone and 3g of palladium catalyst was added to the high-pressure reactor, the reaction temperature of the autoclave was maintained at 100 °C, the pressure of the hydrogenation reaction was maintained at 2.0Mpa, the reaction solution was taken every 2h for the catalytic hydrogenation reaction, tested with liquid chromatography, and the content of trimellitic anhydride was detected to be less than 1%, and the content of 1,2,4-cyclohexanetricartic anhydride was higher than 98%, the hydrogenation reaction was stopped, and after filtering the catalyst, the liquid phase was collected, and part of the solvent was distilled. Finally, 1,2,4-cyclohexane tricarboxylic anhydride solids were obtained. 1,2,4-Cyclohexanetricarboxylic anhydride yield was tested at 95.0%.
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