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Butylparaben

Butylparaben
Butylparaben.svg
Names
IUPAC name
Butyl 4-hydroxybenzoate
Other names
Butyl paraben;
Butyl parahydroxybenzoate;
Butyl p-hydroxybenzoate
Identifiers
94-26-8 YesY
3D model (Jmol) Interactive image
ChEMBL ChEMBL459008 YesY
ChemSpider 6916 YesY
ECHA InfoCard 100.002.108
KEGG D01420 YesY
PubChem 7184
UNII 3QPI1U3FV8 YesY
Properties
C11H14O3
Molar mass 194.23 g·mol−1
Appearance Colorless, odorless, crystalline powder
Melting point 68 to 69 °C (154 to 156 °F; 341 to 342 K)
Slightly soluble
Solubility in acetone, ethanol, chloroform, glycerin, propylene glycol Soluble
Hazards
NFPA 704
Flammability code 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g., canola oil Health code 1: Exposure would cause irritation but only minor residual injury. E.g., turpentine Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Related compounds
Related compounds
Paraben
Ethylparaben
Methylparaben
Propylparaben
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY  (what is YesYN ?)
Infobox references

Butylparaben, or butyl p-hydroxybenzoate, is an organic compound with the formula C
4
H
9
O
2
CC
6
H
4
OH
. It is a white solid that is soluble in organic solvents. It has proven to be a highly successful antimicrobial preservative in cosmetics. It is also used in medication suspensions, and as a flavoring additive in food.

Members of the paraben family are found in fruit and vegetable products, such as barley, flax seed, and grapes. Butylparaben can also be found in low concentrations in liquid and solid medication suspensions, such as tylenol (acetaminophen) and ibuprofen. Butylparaben can also be found in the sewage. A 2001 study found that concentrations of parabens in Danish sewage facilities was to 100 to 1000 times below the acute or chronic effect concentrations.

Butylparaben is prepared by the esterification of 4-hydroxybenzoic acid with 1-butanol in the presence of an acid catalyst such as sulfuric acid. It is produced industrially.

Butylparaben is one of the most common bactericidal/fungicidal additives in cosmetics. It has been used in cosmetic products since the 1940s and in pharmaceutical products since 1924. The popularity of butylparaben in these products is due to its low toxicity in humans and its effective antimicrobial properties, in particular those against mold and yeast. It is now found in more than 20,000 cosmetic products including eye shadow, facial moisturizer/treatment, anti-aging cream, foundation, and sunscreen. It is also used as low-ionic strength solutions as a preservative in some foods and drugs. In most cosmetics paraben is used at low levels, ranging from 0.01 to 0.3%.


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