Dibutoxy ethyl phthalate

Dibutoxy ethyl phthalate
Names
Preferred IUPAC name
Bis(2-butoxyethyl) benzene-1,2-dicarboxylate
Other names
Bis(2-butoxyethyl) phthalate; Kesscoflex; Kronisol; Palatinol K
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.003.831
EC Number
  • 204-213-1
KEGG
UNII
  • InChI=1S/C20H30O6/c1-3-5-11-23-13-15-25-19(21)17-9-7-8-10-18(17)20(22)26-16-14-24-12-6-4-2/h7-10H,3-6,11-16H2,1-2H3
    Key: CMCJNODIWQEOAI-UHFFFAOYSA-N
  • CCCCOCCOC(=O)C1=CC=CC=C1C(=O)OCCOCCCC
Properties
C20H30O6
Molar mass 366.454 g·mol−1
Density 0.93[1]
Hazards
GHS labelling:
GHS09: Environmental hazard
Warning
H413
P273, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
1
0
Lethal dose or concentration (LD, LC):
8380 mg/kg (oral rat)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Dibutoxy ethyl phthalate is an organic compound and phthalate ester, baring 2-butoxyethanol groups. It is used as a plasticizer in polyvinyl chloride, polyvinyl acetate and cellulose acetate. Like most phthalates it is non-volatile, and remains liquid over a wide range of temperatures. Although its water solubility is low, it remains one of the most water soluble of the common phthalates.

References

  1. ^ Paint Testing Manual. ASTM International. 1972. p. 176.
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