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Diuron

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    Diuron
  • Diuron
Cat No: 24040
Biochemicals - Pesticides
Cayman

Diuron is a phenylurea herbicide that inhibits photosynthesis by preventing the formation of ATP and NADH.{42074} It decreases total respiration in roots of wheat by 50% and ground respiration by 100% when used at a concentration of 25 nM/ml.{42073} D...

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This product can only be bought through Cayman Chemical. Please contact us.

Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • N'-(3,4-dichlorophenyl)-N,N-dimethyl-urea
Correlated keywords:
  • 56449-18-4 102962-29-8 127641-75-2 150825-44-8 201749-62-4 2097333-87-2 Biocut-DC-100 DC100 Cardi DCMU-9 99 DCMU9 DCMU99 DMU DP-Hardener-95 Dairon Direx Dironet Dironzol Diurex Diuron-Nortox Duran Dyhard-200 UR-200 UR200 HRT-Dinron HW920 Herbatox Karmax Karmex DW Lucenit Marmer NSC8950 Preventol-A-6 A6 SM400 Telvar Weed Killer UR200 MCF7 Be-Wo anti-fouling UR 200 SM 400 HW 920
Product Overview:
Diuron is a phenylurea herbicide that inhibits photosynthesis by preventing the formation of ATP and NADH.{42074} It decreases total respiration in roots of wheat by 50% and ground respiration by 100% when used at a concentration of 25 nM/ml.{42073} Diuron (2,500 ppm, dietary) increases the incidence of urinary bladder urothelial carcinomas in male and female mice by 73 and 27%, respectively.{42074} It increases the production of reactive oxygen species (ROS) in MCF-7 human breast adenocarcinoma and BeWo human placental choriocarcinoma cells when used at a concentration of 200 µM and reduces viability of BeWo, but not MCF-7, cells when used at concentrations of 50 and 200 µM.{42075} Formulations containing diuron have been used to control broadleaf and grass weeds and as a biocidal antifouling agent.
Size 50 mg
Shipping dry ice
CAS Number 330-54-1
Molecular Formula C9H10Cl2N2O
SMILES ClC1=C(Cl)C=CC(NC(N(C)C)=O)=C1
Molecular Weight 233,1
Formulation A solid
Purity ≥98%
Custom Code 2903.99
UNSPSC code 12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.

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