113585-29-8 Usage
Functionality
Plasticizer
Primary Use
Production of polyvinyl chloride (PVC) plastics
Purpose in PVC
Improves flexibility, durability, and resistance to heat and cold
Additional Applications
Adhesives, sealants, and coatings
Health and Environmental Consideration
Considered a safer alternative to traditional plasticizers like phthalates
Potential Risks
Can still pose some risks and should be handled and used with caution
Chemical Structure
Consists of a benzene ring with two carboxylic acid groups at positions 1 and 3, connected to an ethylene glycol bis(oxy) group, and four ethyl ester groups
Molecular Weight
456.55 g/mol
Physical State
Liquid at room temperature
Color
Clear to slightly yellowish
Odor
Mild to no odor
Solubility
Soluble in most organic solvents, insoluble in water
Boiling Point
Not readily available, but expected to be high due to its molecular weight and structure
Melting Point
Not readily available, but expected to be low due to its plasticizing nature
Density
Not readily available, but expected to be less than water
Viscosity
High viscosity liquid
Volatility
Low volatility due to its high molecular weight and molecular structure
Check Digit Verification of cas no
The CAS Registry Mumber 113585-29-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,8 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113585-29:
(8*1)+(7*1)+(6*3)+(5*5)+(4*8)+(3*5)+(2*2)+(1*9)=118
118 % 10 = 8
So 113585-29-8 is a valid CAS Registry Number.
113585-29-8Relevant academic research and scientific papers
Coordination polymers of flexible tetracarboxylic acids with metal ions. I. Synthesis of CH2- and (CH2)2-spaced bis(oxy)isophthalic acid ligands, and structural characterization of their polymeric adducts with lanthanoid i
Karmakar, Anirban,Goldberg, Israel
experimental part, p. 339 - 349 (2011/10/08)
We report herein on the synthesis and structure of new tetracarboxylic ligands, 5,5′-methylene-bis(oxy)diisophthalic acid and 5,5′-(ethane-1,2-diyl)-bis(oxy)diisophthalic acid, bearing flexible spacers between the two isophthalic acid fragments, as well a
Synthesis, Characterization, and X-ray Structure of the Ruthenium "Picnic-Basket" Porphyrins
Collman, James P.,Brauman, John I.,Fitzgerald, Jeffrey P.,Hampton, Philip D.,Naruta, Yoshinori,et al.
, p. 3477 - 3486 (2007/10/02)
The synthesis and characterization of a new class of sterically protected porphyrins, the "picnic-basket" porphyrins, are presented.These tetraarylporphyrins, which were prepared as cytochrome P-450 active-site analogues, bear a rigid superstucture on one face of the porphyrin macrocycle.The cavity defined by the appended superstructure may be readily varied in size, chirality, and functionality.In addition, the synthesis and characterization, including an X-ray structure, of several ruthenium picnic-basket porphyrin carbonyl complexes are reported.The regiochemistry of axial ligation in these ruthenium derivatives has been determined by 1H NMR spectroscopy.
