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pterostilbene-glutaric acid cocrystal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1304126-72-4

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1304126-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1304126-72-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,4,1,2 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1304126-72:
(9*1)+(8*3)+(7*0)+(6*4)+(5*1)+(4*2)+(3*6)+(2*7)+(1*2)=104
104 % 10 = 4
So 1304126-72-4 is a valid CAS Registry Number.

1304126-72-4Downstream Products

1304126-72-4Relevant academic research and scientific papers

Improving the poor aqueous solubility of nutraceutical compound pterostilbene through cocrystal formation

Bethune, Sarah J.,Schultheiss, Nate,Henck, Jan-Olav

, p. 2817 - 2823 (2011)

Pterostilbene is a nutraceutical compound being investigated for its ability to form cocrystals with pharmaceutically acceptable coformers to improve its poor aqueous solubility. Cocrystals of a 2:1 and 1:1 stoichiometric molar ratio of pterostilbene with piperazine or glutaric acid were synthesized on a multigram scale and fully characterized including single-crystal X-ray diffraction. Furthermore, both cocrystals were evaluated for physical stability with respect to humidity and temperature as well as kinetic solubility. Each cocrystal displayed remarkable stability, showing no evidence of dissociation across a range of durations, temperatures, and relative humidities. The aqueous concentration of pterostilbene measured over five hours from dissolution of the pterostilbene-piperazine cocrystal was six times higher than the solubility of the single-component pterostilbene. Although X-ray powder diffraction results indicate partial transformation of the pterostilbene-piperazine cocrystal to pterostilbene after 5 h, this increase in concentration was sustained throughout the dissolution experiment. Within 5 min of slurrying the pterostilbene- glutaric acid cocrystal in water, precipitation of pterostilbene was observed; thus no dissolution data under these conditions were obtained.

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