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Dibutyl phthalate

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Formula
  
C16H22O4

Molar mass
  
278.34 g/mol

IUPAC ID
  
Dibutyl phthalate

Soluble in
  
Water, Ether, Alcohol

Boiling point
  
340 °C

Density
  
1.05 g/cm³

Melting point
  
-35 °C

Dibutyl phthalate Dibutyl phthalate Wikipedia

Appearance
  
Colorless to faint yellow oily liquid

Dibutyl phthalate


Dibutyl phthalate (DBP) is a commonly used plasticizer. It is also used as an additive to adhesives or printing inks. It is soluble in various organic solvents, e.g. in alcohol, ether and benzene. DBP is also used as an ectoparasiticide. DBP is also a putative endocrine disruptor

Contents

Dibutyl phthalate Dibutyl Phthalate

European Union

Dibutyl phthalate NF Monographs Dibutyl Phthalate

The use of this substance in cosmetics, including nail polishes, is banned in the European Union under Directive 76/768/EEC 1976.

The use of DBP has been restricted in the European Union for use in children's toys since 1999.

Dibutyl phthalate wwwsigmaaldrichcomcontentdamsigmaaldrichstr

An EU Risk Assessment has been conducted on DBP and the final outcome has now been published in the EU Official Journal. To eliminate a potential risk to plants in the vicinity of processing sites and workers through inhalation, measures are to be taken within the framework of the IPPC Directive (96/61/EC) and the Occupational Exposure Directive (98/24/EC) Also includes the 2004 addendum.

United States

Dibutyl phthalate Dibutyl phthalate C16H22O4 ChemSpider

DBP was added to the California Proposition 65 (1986) list of suspected teratogens in November 2006. It is a suspected endocrine disruptor. It was used in some nail polishes; all major producers began eliminating this chemical from nail polishes in the Fall of 2006.

DBP was permanently banned in children's toys, in concentrations of 1000 ppm or greater, under section 108 of the Consumer Product Safety Improvement Act of 2008 (CPSIA).

Production

DBP is produced by the reaction of n-butanol with phthalic anhydride. It is or was produced in the United States by Eastman Chemical Company, but the company announced in March 2011 that it would end production and exit the DBP and DEP (diethyl phthalate) market in December 2011.

Exposure

Based on urine samples from people of different ages, the European Commission Scientific Committee on Health and Environmental Risks (SCHER) concluded that total exposures to individual phthalates in the general population are below tolerable daily intakes (TDI), except in the case of DBP for which efforts to further reduce exposures are needed.

Biodegradation

The white rot fungus Polyporus brumalis degrades DBP.

References

Dibutyl phthalate Wikipedia