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1,3-Benzenedicarboxylic acid, 5,5'-[1,6-hexanediylbis(oxy)]bis-, also known as bis(2-hydroxyethyl) terephthalate or BHT, is a chemical compound with the molecular formula C20H22O8. It is a white crystalline solid that is soluble in most organic solvents and slightly soluble in water. BHT is primarily used as an antioxidant and a preservative in various applications, including food, cosmetics, and industrial products, to prevent oxidation and spoilage. It is also used as a stabilizer in polymers and as a flame retardant. The compound is synthesized by reacting terephthalic acid with ethylene glycol, resulting in a product that has a molecular weight of 390.38 g/mol.

22937-73-1

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22937-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22937-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,3 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22937-73:
(7*2)+(6*2)+(5*9)+(4*3)+(3*7)+(2*7)+(1*3)=121
121 % 10 = 1
So 22937-73-1 is a valid CAS Registry Number.

22937-73-1Downstream Products

22937-73-1Relevant academic research and scientific papers

Synthesis and Analysis of Telechelic Polyisobutylenes for Hydrogen-Bonded Supramolecular Pseudo-Block Copolymers

Binder, Wolfgang H.,Kunz, Michael J.,Kluger, Christian,Hayn, Getraud,Saf, Robert

, p. 1749 - 1759 (2007/10/03)

New telechelic polyisobutylenes (PIB) with hydrogen-bonding motifs were prepared. Nucleobases such as thymine, uracil, and cytosine as well as chelate-type hydrogen-bonding donor-acceptors were affixed onto the end groups of the PIB. Starting with PIB of

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.

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