677010-20-7

Basic information

• Product Name: Biphenyl-3,4′,5-tricarboxylic acid
• Synonyms: Biphenyl-3,4′,5-tricarboxylic acid;Biphenyl-3,4',5-tricarboxylic acid 96%;5-(4-carboxyphenyl)benzene-1,3-dicarboxylicacid;[1,1'-biphenyl]-3,4',5-tricarboxylic acid
• CAS NO: 677010-20-7
• Molecular Formula: C₁₅H₁₀O₆
• Molecular Weight: 286.2363
• Product Categories: MOFS COFS
• Mol File: 677010-20-7.mol
• Article Data: 7

Chemical Properties

• Melting Point: >300°C
• Boiling Point: 627.7±55.0 °C(Predicted)
• Appearance: /
• Density: 1.488±0.06 g/cm3(Predicted)
• PKA: 3.36±0.10(Predicted)
• CAS DataBase Reference: Biphenyl-3,4′,5-tricarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: Biphenyl-3,4′,5-tricarboxylic acid(677010-20-7)
• EPA Substance Registry System: Biphenyl-3,4′,5-tricarboxylic acid(677010-20-7)

Safety Data

• Hazard Codes: Xi,N
• Statements: 36/37/38-50
• Safety Statements: 26-61
• RIDADR: UN 3077 9 / PGIII
• WGK Germany: 3
• Hazardous Substances Data: 677010-20-7(Hazardous Substances Data)

Usage

General Description

This product has been enhanced for energy efficiency.

Upstream product

• 51760-21-5 dimethyl 5-bromoisophthalate 
• 23351-91-9 5-bromoisophthalic acid 
• 121-91-5 isophthalic acid 
• 99768-12-4 4-methoxycarbonylphenylboronic acid 
• 99-31-0 5-aminoisophthalic acid 
• 51839-15-7 5-iodo-isophthalic acid dimethyl ester 
• 99-27-4 dimethyl 5-aminoisophthalate 
• 944392-68-1 dimethyl 5-(pinacolboryl)isophthalate 
• 5720-05-8 4-methylphenylboronic acid 
• 7383-87-1 1-(4-methylphenyl)-3,5-dimethylbenzene 

Downstream Products

• 1629958-55-9 {[Zn(HBPT)(1,3-bis(imidazol-1-ylmethyl)benzene)]*H₂O}_n 

Relevant articles and documents

Porous crystal derived from a tricarboxylate linker with two distinct binding motifs

The use of a reduced symmetry organic linker for the preparation of porous coordination polymers is demonstrated. The solvothermal reaction of the unsymmetrically substituted biaryl compound biphenyl-3,4′,5-tricarboxylic acid with Cu(II) ions produces a [3,4,6]-connected coordination polymer exhibiting very high porosity and surface area (SLangmuir = 3100 m2/g). A striking feature of the structure is its incorporation, in a single material, of both the ubiquitous dinuclear Cu(II) paddlewheel motif and the rarely observed trinuclear Cu(II) cluster. Saturation H2 uptake, measured at 77 K, shows an excess gravimetric uptake of 5.7 wt % at 45 bar with a steep rise at low pressures. Copyright

Monocrystalline iron metal organic frameworks

The invention relates to large single crystals of iron metal-organic framework materials comprising at least one iron metal ion, processes for preparing the same, methods for employing the same, and the use thereof. The invention also relates to monocrystalline and polycrystalline iron metal-organic frameworks.

Removal of toxic dyes from aqueous medium using adenine based bicomponent hydrogel

By utilizing hydrogen bonding and π-π stacking interactions, we have demonstrated the construction of three dimensional adenine based gel networks due to the self assembly with complementary tricarboxylic acid derivatives which were designed and unambiguously characterized with the help of NMR, HRMS, and FTIR. Upon cooling the homogeneous aqueous solution of adenine and tricarboxylic acid, it formed hydrogels which were thermoreversible in nature and characterized by various instrumental techniques such as OM, FESEM, TEM, AFM, FL, XRD, FT-IR, rheology etc. Networks of belts in the hydrogel were clearly observed and the dimension of belt depended on the tricarboxylic acid used. The intermolecular hydrogen bonds which were considered to be the driving force for the formation of stable gel were confirmed by FT-IR studies. In spite of the absence of symmetry either in bpca or adenine, these two moieties surprisingly produced gels and it was due to the symmetrical position of complementary interaction sites between adenine and tricarboxylic acids. The mechanical strength of the hydrogel network as revealed by rheological study depended on the tricarboxylic acid used in the two-component systems and also on the composition of fixed pair. These kind of hydrogels have potential to be utilized as inexpensive materials for the treatment of waste water containing organic dyes (methylene blue, rhodamine 6G and crystal violet) that are widely used in textile as well as dye industries.