Dibutyl phthalate

Dibutyl phthalate

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Dibutyl phthalate
Names

IUPAC name

Dibutyl phthalate

Other names

Di-n-butyl phthalate, Butyl phthalate, n-Butyl phthalate, 1,2-Benzenedicarboxylic acid dibutyl ester, o-Benzenedicarboxylic acid dibutyl ester, DBP, Palatinol C, Elaol, Dibutyl-1,2-benzene-dicarboxylate

Identifiers
CAS Registry Number
ATC code
ChEBI
ChEMBL
ChemSpider
EC number
InChI[show]
IUPHAR/BPS
Jmol-3D images
KEGG
PubChem
RTECS number
SMILES[show]
UNII
Properties
Chemical formula
Molar mass
Appearance
Odor
Density
Melting point
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Solubility in water
log P
Vapor pressure
Hazards
Main hazards
R-phrases
S-phrases
NFPA 704
Flash point
Autoignition
temperature
Explosive limits
Lethal dose or concentration (LDLC):
LD50 (Median dose)
LC50 (Median concentration)
US health exposure limits (NIOSH):
PEL (Permissible)
REL (Recommended)
IDLH (Immediate danger
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

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 alcoholether and benzene. DBP is also used as an ectoparasiticide.

Contents

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Legislative control[edit]

European Union[edit]

The use of this substance in cosmetics, including nail polishes, is banned in the European Union under Directive 76/768/EEC 1976.[3]

The use of DBP has been restricted in the European Union for use in children's toys since 1999.[4]

United States[edit]

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[edit]

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.[5]

Exposure[edit]

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.[6]

Biodegradation[edit]

The white rot fungus Polyporus brumalis degrades DBP. [7]

See also[edit]

References[edit]

  1. Jump up to:a b c d "NIOSH Pocket Guide to Chemical Hazards #0187"National Institute for Occupational Safety and Health (NIOSH).

  2. Jump up to:a b "Dibutyl Phthalate". Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health (NIOSH).

  3. Jump up^ EU Council Directive 76/768/EEC of 27 July 1976 on the approximation of the laws of the Member States relating to cosmetic products

  4. Jump up^ Ban of phthalates in childcare articles and toys, press release IP/99/829, 10 November 1999

  5. Jump up^ "Eastman Announces Discontinuation of Manufacture of DEP and DBP Plasticizers". Eastman. March 16, 2011.

  6. Jump up^ "Phthalates in school supplies". GreenFacts Website. Retrieved 2009-06-10.

  7. Jump up^ Ishtiaq Ali, Muhammad (2011). Microbial degradation of polyvinyl chloride plastics (PDF) (Ph.D.). Quaid-i-Azam University. p. 48.

External links[edit]

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Health issues of plastics and Polyhalogenated compounds (PHCs)

PlasticizersPhthalates
Miscellaneous plasticizers
Monomers
Miscellaneous additives incl. PHCs
Health issues
Miscellanea

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