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Dipentaerythritol

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Dipentaerythritol Basic information

Product Name:
Dipentaerythritol
Synonyms:
  • Dipentaerythritol(Di-PE)
  • 2,2'[OXYBIS(METHYLEN)]BIS[HYDROXYMETHYL]-1,3-PROPANDIOL
  • 2,2,6,6,-Tetra(hydroxymethyl)-4-oxaheptane-1,7-diol
  • 2,2,2',2'-tetrakis(hydroxymethyl)-3,3'-oxydipropan-1-ol
  • 2-([3-Hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl)-2-(hydroxymethyl)-1,3-propanediol
  • 2,2'-(Oxybis(methylene))bis-((hydroxymethyl)-1,3-propanediol)
  • 2,2’-(oxybis(methylene))bis(2-(hydroxymethyl)-3-propanediol
  • DIPENTAERYTHRITOL FOR SYNTHESIS
CAS:
126-58-9
MF:
C10H22O7
MW:
254.28
EINECS:
204-794-1
Product Categories:
  • Fine Chemical
  • Building Blocks
  • Organic Building Blocks
  • Chemical Synthesis
  • Organic Building Blocks
  • Oxygen Compounds
  • Oxygen Compounds
  • Polyols
Mol File:
126-58-9.mol
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Dipentaerythritol Chemical Properties

Melting point:
215-218 °C (lit.)
Boiling point:
356°C
Density 
1.36 g/cm3 (20℃)
vapor pressure 
<0.00001 hPa (20 °C)
refractive index 
1.4455 (estimate)
storage temp. 
Store below +30°C.
solubility 
2.4g/l
form 
Crystalline Powder
pka
13.38±0.10(Predicted)
color 
White
PH
5 (2g/l, H2O, 20℃)
Water Solubility 
0.29 g/100 mL (20 ºC)
Sensitive 
Hygroscopic
InChIKey
TXBCBTDQIULDIA-UHFFFAOYSA-N
LogP
1.8 at 23℃
CAS DataBase Reference
126-58-9(CAS DataBase Reference)
NIST Chemistry Reference
1,3-Propanediol, 2,2'-[oxybis(methylene)]bis[2-(hydroxymethyl)-(126-58-9)
EPA Substance Registry System
Dipentaerythritol (126-58-9)
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Safety Information

Safety Statements 
24/25
WGK Germany 
1
Autoignition Temperature
370 °C
TSCA 
Yes
HS Code 
29094919
Hazardous Substances Data
126-58-9(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: > 2000 mg/kg

MSDS

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Dipentaerythritol Usage And Synthesis

Description

Dipentaerythritol, also known as 2,2-[oxybis(methylene)- bis[2-hydroxymethyl]-1,3-propanediol, is a byproduct of pentaerythritol production. Because of its low solubility in water (0.22 g/ 100 g H2O at 20 ℃ and 10.0 g/100 g H2O at 100 ℃) it can be separated from pentaerythritol by fractional crystallization. The yield can be increased by changing the ratio of formaldehyde/ acetaldehyde towards stoichiometric. Adding pentaerythritol before starting the reaction also increases the yield. An effective method is to use acrolein instead of acetaldehyde. Dipentaerythritol can be produced intentionally from pentaerythritol by acid catalysis. Dipentaerythritol is purified as a coproduct by many pentaerythritol producers.

Chemical Properties

white crystalline powder

Uses

2,2''-(Oxybis(methylene))bis(2-(hydroxymethyl)-propane-1,3-diol) is used in preparation of new type of explosion-proof and flame-retardant tape material for cables.

Application

Dipentaerythritol (DPE) is an attractive raw material used for the production of polyesters, polyethers, polyurethanes, alkyd resins, photosensitive resin film. DPE is also employed in a wide range synthesis of specialty chemicals such as lubricants, coatings, adhesives, plasticizers and cosmetics.

Preparation

Dipentaerythritol is obtained as a byproduct in the manufacture of pentaerythritol; it is separated by fractional distillation.

Dipentaerythritol (DPE) has been prepared from a slurry of Pentaerythritol (PE) in sulfolane catalyzed by a low amount of sulfuric acid and was isolated with 16% yield (72% GPC purity) and 57% isolated selectivity.
synthesis of dipentaerythritol from pentaerythritol under acidic conditions

Application

PVC stabilizers based on calcium – zinc carboxylates use micronized dipentaerythritol as costabilizer to improve the thermal stability of PVC during processing. This system grows fast in economic significance at the expense of leadbased stabilizers due to environmental reasons. Micronized dipentaerythritol is also used in intumescent paints. Synthetic lubricants are another important application for dipentaerythritol. The C5 – C10 esters are used as lubricants in jet engines and refrigerators. Rosin esters made from dipentaerythritol have a higher softening point than rosin esters from pentaerythritol.

Flammability and Explosibility

Not classified

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