441325-60-6 Usage
Chemical structure
Ester formed from propanol and gallic acid
Production method
Esterification of gallic acid with propanol
Applications
a. Antioxidant and preservative in the food industry
b. Extends shelf life of edible fats, oils, and salad dressings
c. Used in cosmetics, pharmaceuticals, and other industrial applications
Function
Prevents oxidation of fats and oils
Chemical properties
a. Ester compound
b. Derived from the reaction of an alcohol (propanol) and a carboxylic acid (gallic acid)
Physical properties
a. Solid at room temperature
b. May vary in color depending on purity and source
Safety
Generally recognized as safe (GRAS) by the US FDA for use in the food industry
Regulatory information
9CI (Chemical Abstracts Service Registry Number) 1,4-Benzenediol, 2-(phenylmethoxy)-
Check Digit Verification of cas no
The CAS Registry Mumber 441325-60-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,1,3,2 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 441325-60:
(8*4)+(7*4)+(6*1)+(5*3)+(4*2)+(3*5)+(2*6)+(1*0)=116
116 % 10 = 6
So 441325-60-6 is a valid CAS Registry Number.
441325-60-6Relevant articles and documents
Synthesis of the reported structure of the bisbenzoquinone lanciaquinone, isolated from Maesa lanceolata
Guillonneau, Loic,Taddei, David,Moody, Christopher J.
supporting information; experimental part, p. 4505 - 4508 (2009/05/27)
(Chemical Equation Presented) Lanciaquinone, isolated from Maesa lanceolate, was originally assigned as a bisbenzoquinone with a C 14-chain linking the two quinone rings. A synthesis of the reported structure, in which the key step is a double Clalsen rearrangement, suggests that the structure of the natural product needs to be revised.
