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C 5 H 9 NO: N-Methyl-2-pyrrolidone: 872-50-4 CH 3 CH 2 CH 2 OH: 1-Propanol: 71-23-8 CH 2 (CH 2 OH) 2: 1,3-Propanediol: 504-63-2 HOCH 2 CH 2 CH 2 CH 2 CH 2 OH: 1,5-Pentanediol: 111-29-5 (CH 3) 2 CHOH: 2-Propanol: 67-63-0 CH 3 CH 2 COOH: propanoic acid: 79-09-4 HOCH 2 CHOHCH 3: propylene glycol: 57-55-6 C 5 H 5 N: pyridine: 110-86-1 C 4 H 8 O 2 S ...
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 .
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 ...
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
Common cosolvents for this purpose are ethanol, propylene glycol, glycerine, glycofural, and polyethylene glycols. [7] The effect of cosolvency on drug solubilization can be great, as evidenced by a 2009 study in which researchers from Panjab University showed the solubility of various anti-diabetic drugs increase by more than 500 times by use ...
1,5-Pentanediol; Pinacol; Prenderol; 1,3-Propanediol; Propylene glycol This page was last edited on 12 July 2024, at 00:49 (UTC). Text is available under the ...
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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 .
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