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115983

Sigma-Aldrich

Trimethyl 1,3,5-benzenetricarboxylate

98%

Synonym(s):

Trimesic acid trimethyl ester, Trimethyl trimesate

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About This Item

Linear Formula:
C6H3(CO2CH3)3
CAS Number:
Molecular Weight:
252.22
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

solid

mp

145-147 °C (lit.)

SMILES string

COC(=O)c1cc(cc(c1)C(=O)OC)C(=O)OC

InChI

1S/C12H12O6/c1-16-10(13)7-4-8(11(14)17-2)6-9(5-7)12(15)18-3/h4-6H,1-3H3

InChI key

RGCHNYAILFZUPL-UHFFFAOYSA-N

Related Categories

Application

Trimethyl 1,3,5-benzenetricarboxylate has been used to synthesize yttrium trimesates with open frameworks.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Bao-Xia Dong et al.
Dalton transactions (Cambridge, England : 2003), 39(24), 5683-5687 (2010-05-21)
Two novel yttrium trimesates with open frameworks have been synthesized by the self-assembly of trimethyl 1,3,5-benzenetricarboxylate and Y(3+) ion in mixed solvent of dimethylformamide (DMF)/water and diethylformamide (DEF)/water, where changes of solvents with different molecular sizes lead to the formation
Sheng-Mu You et al.
Nanomaterials (Basel, Switzerland), 10(9) (2020-09-02)
Photoelectrochemical (PEC) water splitting is a promising strategy to improve the efficiency of oxygen evolution reactions (OERs). However, the efficient adsorption of visible light as well as long-term stability of light-harvesting electrocatalysis is the crucial issue in PEC cells. Metal-organic

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