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1,3-Propanediol is the organic compound with the formula CH 2 (CH 2 OH) 2. This 3-carbon diol is a colorless viscous liquid that is miscible with water. Products
Estimates on the prevalence of propylene glycol allergy range from 0.8% (10% propylene glycol in aqueous solution) to 3.5% (30% propylene glycol in aqueous solution). [ 70 ] [ 71 ] [ 72 ] The North American Contact Dermatitis Group (NACDG) data from 1996 to 2006 showed that the most common site for propylene glycol contact dermatitis was the ...
Another example is propane-1,2-diol, or alpha propylene glycol, HO−CH 2 −CH(OH)−CH 3, used in the food and medicine industry, as well as a relatively non-poisonous antifreeze product. On commercial scales, the main route to vicinal diols is the hydrolysis of epoxides .
The following compounds are liquid at room temperature and are completely ... C 4 H 10 O 2: dimethoxyethane: 110-71-4 (CH ... propylene glycol: 57-55-6 C 5 H 5 N ...
Bioseparation of 1,3-propanediol is a biochemical process for production of 1,3-propanediol (PDO). PDO is an organic compound with many commercial applications. Conventionally, PDO is produced from crude oil products such as propylene or ethylene oxide .
Propylene glycol dinitrate (PGDN, 1,2-propylene glycol dinitrate, or 1,2-propanediol dinitrate) is an organic chemical, an ester of nitric acid and propylene glycol. It is structurally similar to nitroglycerin , except that it has one fewer nitrate group.
The available moisture determines microbial activity, physical properties, sensory properties and the rate of chemical changes, that if not controlled, are the cause of reduced shelf life. [10] Examples are dry cereal with semi-moist raisins , ice cream in a cone, chocolate , hard candy with liquid centers and cheese .
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