Clofibric acid
Structural formula | |||||||||||||||||||
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General | |||||||||||||||||||
Surname | Clofibric acid | ||||||||||||||||||
other names |
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Molecular formula | C 10 H 11 ClO 3 | ||||||||||||||||||
Brief description |
white solid |
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External identifiers / databases | |||||||||||||||||||
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properties | |||||||||||||||||||
Molar mass | 214.65 g mol −1 | ||||||||||||||||||
Physical state |
firmly |
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density |
1.23 g cm −3 |
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Melting point |
119-120 ° C |
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solubility |
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safety instructions | |||||||||||||||||||
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Toxicological data | |||||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Clofibric acid is a chemical compound from the group of aryloxyalkanecarboxylic acids .
Extraction and presentation
Clofibric acid can be obtained by reacting p-chlorophenol with acetone and chloroform in the presence of sodium hydroxide .
properties
Clofibric acid is a white solid that is sparingly soluble in water.
use
Clofibric acid and its derivatives are used as a drug to lower blood cholesterol . The related compound mecoprop is used as a plant growth regulator.
safety instructions
Some derivatives of clofibric acid known as fibrates (for example clofibrate or bezafibrate ) are metabolized to form this in the body. This accumulates in the groundwater due to its high microbial persistence and low sorption capacity .
Individual evidence
- ↑ a b c d e f g Data sheet 2- (4-Chlorophenoxy) isobutyric acid, 98% from AlfaAesar, accessed on March 4, 2018 ( PDF )(JavaScript required) .
- ^ Carl L. Yaws: Thermophysical Properties of Chemicals and Hydrocarbons . William Andrew, 2014, ISBN 978-0-323-29060-9 , pp. 308 ( limited preview in Google Book search).
- ^ A b Olivier Thomas, Christopher Burgess: UV-Visible Spectrophotometry of Water and Wastewater . Elsevier, 2017, ISBN 978-0-444-63900-4 , pp. 447 ( limited preview in Google Book search).
- ↑ PPDB: clofibric acid , accessed March 4, 2018
- ↑ Data sheet 2- (p-Chlorophenoxy) -2-methylpropionic acid, 97% from Sigma-Aldrich , accessed on March 4, 2018 ( PDF ).
- ^ Clemens Lamberth, Jürgen Dinges: Bioactive Carboxylic Compound Classes Pharmaceuticals and Agrochemicals . John Wiley & Sons, 2016, ISBN 978-3-527-69396-2 , pp. 47 ( limited preview in Google Book search).
- ↑ E. Oberdisse, E. Hackenthal: Pharmacology and Toxicology . Springer-Verlag, 2013, ISBN 978-3-642-56314-0 , pp. 555 ( limited preview in Google Book search).
- ↑ clofibric acid data sheet , accessed March 4, 2018.
- ↑ Traugott Scheytt, Susanne Grams, Holger Fell: Occurrence and behavior of a drug (clofibric acid) in groundwater . In: groundwater . tape 3 , no. 2 , June 1, 1998, pp. 67-77 , doi : 10.1007 / s767-1998-8568-1 ( PDF ).
- ↑ Traugott Scheytt, Susanne Grams, Holger Fell: Occurrence and behavior of a drug (clofibric acid) in groundwater. In: groundwater. 3, 1998, p. 67, doi : 10.1007 / s767-1998-8568-1 .