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Dipentaerythritol
[CAS# 126-58-9]

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Identification
Classification Chemical reagent >> Organic reagent >> Fatty alcohol
Name Dipentaerythritol
Synonyms 2,2,6,6,-Tetra(hydroxymethyl)-4-oxaheptane-1,7-diol; 2,2,2',2'-Tetrakis(hydroxymethyl)-3,3'-oxydipropan-1-ol
Molecular Structure CAS # 126-58-9, Dipentaerythritol, 2,2,6,6,-Tetra(hydroxymethyl)-4-oxaheptane-1,7-diol, 2,2,2',2'-Tetrakis(hydroxymethyl)-3,3'-oxydipropan-1-ol
Molecular Formula C10H22O7
Molecular Weight 254.28
CAS Registry Number 126-58-9
EC Number 204-794-1
SMILES C(C(CO)(CO)COCC(CO)(CO)CO)O
Properties
Melting point 215-225 ºC
Boiling point 356 ºC
Water solubility 0.29 g/100 mL (20 ºC)
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319-H335    Details
Precautionary Statements P261-P305+P351+P338    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Specific target organ toxicity - single exposureSTOT SE3H335
Eye irritationEye Irrit.2H319
SDS Available
up Discovory and Applicatios
Dipentaerythritol is a versatile chemical compound known for its unique structure and wide-ranging applications in industrial and material sciences. As an extended form of pentaerythritol, dipentaerythritol features two additional hydroxymethyl groups, enhancing its reactivity and utility in various chemical processes.

The discovery of dipentaerythritol followed the study of pentaerythritol, which is widely used in the synthesis of polyols and resins. Dipentaerythritol was identified as a valuable compound due to its enhanced functionality, making it suitable for more specialized applications. The synthesis of dipentaerythritol typically involves the reaction of pentaerythritol with formaldehyde or similar reagents under controlled conditions to extend the hydroxymethyl groups.

One of the primary applications of dipentaerythritol is in the production of high-performance resins and coatings. Its ability to form complex cross-linked structures makes it an ideal component in the synthesis of alkyd resins, which are used in various coatings, paints, and varnishes. These resins benefit from the enhanced chemical and physical properties imparted by dipentaerythritol, including improved hardness, durability, and resistance to environmental factors.

In addition to its role in resins, dipentaerythritol is used in the production of plasticizers and stabilizers for plastics. The compound's structure provides excellent compatibility with different polymers, enhancing their flexibility, strength, and thermal stability. This makes dipentaerythritol a valuable ingredient in the manufacturing of high-quality plastic materials used in automotive, construction, and consumer goods.

Dipentaerythritol also finds applications in the field of pharmaceuticals and fine chemicals. Its reactivity allows it to be used as an intermediate in the synthesis of various active pharmaceutical ingredients and specialty chemicals. The compound's ability to form complex molecules with high precision makes it useful in designing and producing compounds with specific biological activities or chemical properties.

Despite its advantageous properties, the handling of dipentaerythritol requires proper safety measures due to its reactive nature. Adequate precautions are necessary during its synthesis and application to ensure safe use in industrial processes.

Overall, dipentaerythritol represents a significant advancement in the field of chemical synthesis and material science. Its ability to enhance the properties of resins, plastics, and pharmaceuticals underscores its importance in various industrial applications.
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