DCMU

You don't need to be Editor-In-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this page. Next enter or edit the information that you would like to appear here. Once you are done editing, scroll down and click the Save page button at the bottom of the page.

Jump to: navigation, search
Dcmu
Image:Diuron.png
General
Name DCMU
Chemical name Diuron, 3-(3,4-dichlorophenyl)-1,1-dimethylurea
Empirical formula C9H10Cl2N2O
CAS registry number 330-54-1
Properties
Molecular mass 233.10 g/mol
Density 1.48 g/cm³
Melting point 158 °C
Boiling point 180 °C
Vapor pressure 1.1 mPa (25 °C)
Solubility water soluble (42 mg/L)
Safety
Hazard symbol
Harmful Dangerous for the environment
Threshold Limit Value 5 mg/m³
Except where noted otherwise, data are given for
materials in their standard state (at 25 °C, 100 kPa)
Infobox disclaimer and references

DCMU (3-(3,4-dichlorophenyl)-1,1-dimethylurea) is a herbicide that inhibits photosynthesis. It was released by Bayer in 1954 under the name of Diuron.

Mechanism of action

DCMU is a very specific and sensitive inhibitor of photosynthesis. It blocks the plastoquinone binding site of photosystem II, disallowing the electron flow from where it is generated, in photosystem II, to plastoquinone. This interrupts the photosynthetic electron transport chain in photosynthesis and thus blocks the ability of the plant to turn light energy into chemical energy (ATP and reductant potential).

DCMU only blocks electron flow from photosystem II, it has no effect on photosystem I or other reactions in photosynthesis, such as light absorption or carbon fixation in the Calvin cycle.

Because it absorbs electrons oxidized from water in PS II, the electron "hole" of PS I cannot be satisfied, effectively shutting down photosynthesis by blocking the reduction of NADP+ to NADPH, and the cyclic photosynthetic pathway since electron shuttling is associated with proton pumping across the membrane into the lumen.

Applications

Besides its use a herbicide, DCMU is often used to research energy flow in photosynthesis.de:DCMUfr:Diuron nl:Diuron


Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

Personal tools
In other languages