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14295-64-8

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14295-64-8 Usage

Description

Glycerol triisobutyrate, also known as triisobutyrin, is a low-molecular weight glycerol triester derived from glycerol and isobutyric acid. It is a colorless, odorless liquid with a slight ester-like smell and is known for its plasticizing properties.

Uses

Used in Plastic Industry:
Glycerol triisobutyrate is used as a plasticizer for poly(vinyl chloride) (PVC) to enhance the flexibility, workability, and processability of the material. Its low molecular weight allows it to penetrate the polymer matrix effectively, reducing the glass transition temperature and improving the overall plasticity of PVC.

Check Digit Verification of cas no

The CAS Registry Mumber 14295-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,9 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14295-64:
(7*1)+(6*4)+(5*2)+(4*9)+(3*5)+(2*6)+(1*4)=108
108 % 10 = 8
So 14295-64-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O6/c1-9(2)13(16)19-7-12(21-15(18)11(5)6)8-20-14(17)10(3)4/h9-12H,7-8H2,1-6H3

14295-64-8Downstream Products

14295-64-8Relevant articles and documents

Widely useful DMAP-catalyzed esterification under auxiliary base- and solvent-free conditions

Sakakura, Akira,Kawajiri, Kimio,Ohkubo, Takuro,Kosugi, Yuji,Ishihara, Kazuaki

, p. 14775 - 14779 (2008/09/17)

With regard to atom economy and E-factor, catalytic condensation of carboxylic acids with equimolar amounts of alcohols is the most desirable. Although several highly active dehydration catalysts have been reported, more efficient alternatives are still strongly needed because the dehydrative esterification of tertiary alcohols, phenols, acid-sensitive alcohols, amino acids, and hardly soluble alcohols has never proceeded satisfactorily. Here we report new insights into the classical DMAP-catalyzed acylation of alcohols: surprisingly, only a 0.05-2 mol % of DMAP can efficiently promote acylation of alcohols with acid anhydrides under auxiliary base- and solvent-free conditions to give the corresponding esters in high yields. Furthermore, we achieved the recovery and reuse of commercially available polystyrene-supported DMAP without using any solvents. These serendipitous findings provide widely useful and environmentally benign esterification methods, which might be more practical and reliable than catalytic dehydrative condensation methods, in particular, for the less reactive alcohols which hardly condense with carboxylic acid directly.

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