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Dibutyl sebacate

Dibutyl sebacate[1]
Dibutyl sebacate.svg
Names
Other names
dibutyl sebacate, Proviplast 1944lkl;
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.003.339 Edit this at Wikidata
EC Number
  • 203-672-5
RTECS number
  • VS1150000
UNII
CompTox Dashboard (EPA)
Properties
C18H34O4
Molar mass 314.466 g·mol−1
Appearance colorless liquid
Density 0.9405 g/cm3 at 15 °C
Melting point −10 °C (14 °F; 263 K)
Boiling point 344.5 °C (652.1 °F; 617.6 K)
0.04 g/L
Solubility soluble in diethyl ether, carbon tetrachloride
Structure
2.48 D
Thermochemistry
1.968 J·g−1·K−1
Hazards
GHS pictograms GHS07: Harmful
GHS Signal word Warning
GHS hazard statements
H315, H319, H335
GHS precautionary statements
P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501
Flash point 178 °C (352 °F; 451 K)
365 °C (689 °F; 638 K)
Explosive limits >0.4%
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Dibutyl sebacate (DBS) is an organic chemical, a dibutyl ester of sebacic acid. Its main use is as a plasticizer in production of plastics, namely cellulose acetate butyrate, cellulose acetate propionate, ethyl cellulose, polyvinyl butyral, polyvinyl chloride, polystyrene, and many synthetic rubbers (especially nitrile rubber and neoprene) and other plastics. It can be used for plastics in use in the food packaging industry, in plastics used for medical devices, and for pharmaceutical applications, e.g. as a plasticizer for film coating of tablets, beads, and granules.[2] It is also used as a lubricant in shaving lotions, and a flavoring additive in non-alcoholic beverages, ice cream, ices, candy, and baked goods. It provides excellent compatibility with a range of plastic materials, superior properties at low temperatures, and good oil resistivity. Its other names include Morflex, Kodaflex, polycizer, Proviplast 1944 and PX 404. Dibutyl sebacate is also used as a desensitizer in Otto fuel II, a torpedo monopropellant.

References

  1. ^ Lide, David R. (1998). Handbook of Chemistry and Physics (87 ed.). Boca Raton, Florida: CRC Press. pp. 3–162, 15–18. ISBN 0-8493-0594-2.
  2. ^ chemicalland21.com Dibutyl Sebacate Archived 2010-01-30 at the Wayback Machine
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