Dibutyl phthalate

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Dibutyl phthalate
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
Identifiers
CAS number [84-74-2]
PubChem 3026
EINECS number 201-557-4
RTECS number TI0875000
Properties
Molecular formula C16H22O4
Molar mass 278.35 g/mol
Appearance Colorless oily liquid
Density 1.05 g/cm3 at 20 °C
Melting point

-35 °C

Boiling point

340 °C

Solubility in water 0.013 g/l
log P 4.72
Hazards
Main hazards Dangerous for the environment (N), Harmful (Xi)
NFPA 704
1
1
0
 
R-phrases R50, R61, R62
S-phrases S45, S53, S61
Flash point 157 °C c.c.
Autoignition
temperature
402 °C
Explosive limits 0.5 - 3.5%
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox disclaimer and references

Template:US centric

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

Contents

[edit] Production

Production of DBP by direct esterification of n-butanol and phthalic anhydride

[edit] Obesity

A study on CDC data published in Environmental Health Perspectives (EHP), revealed that American men with abdominal obesity or insulin resistance (a precursor to diabetes) were more likely to have high levels of DEHP and DBP metabolites in their urine than men without those problems.[1]


[edit] See also

[edit] External links