32427

Orthosulfamuron

PESTANAL^®, analytical standard

• Szinonimák: 1-(4,6-Dimethoxy-2-pyrimidinyl)-3-[2-(dimethylcarbamoyl)phenylsulfamoyl]urea
• Tapasztalati képlet (Hill-képlet): C₁₆H₂₀N₆O₆S
• CAS-szám: 213464-77-8
• Molekulatömeg: 424.43
• Beilstein: 11343666
• MDL-szám: MFCD09027340
• UNSPSC kód: 41116107
• PubChem Substance ID: 329754205
• NACRES: NA.24

Tulajdonságok

• grade: analytical standard
• Minőségi szint: 100
• termékcsalád: PESTANAL^®
• eltarthatósági idő: limited shelf life, expiry date on the label
• technika/technikák: HPLC: suitable; gas chromatography (GC): suitable
• alkalmazás(ok): agriculture; environmental
• format: neat
• SMILES string: COc1cc(OC)nc(NC(=O)NS(=O)(=O)Nc2ccccc2C(=O)N(C)C)n1
• InChI: 1S/C16H20N6O6S/c1-22(2)14(23)10-7-5-6-8-11(10)20-29(25,26)21-16(24)19-15-17-12(27-3)9-13(18-15)28-4/h5-9,20H,1-4H3,(H2,17,18,19,21,24)
• Nemzetközi kémiai azonosító kulcs: UCDPMNSCCRBWIC-UHFFFAOYSA-N

Leírás

Általános leírás

Orthosulfamuron is a systemic post-emergence herbicide belonging to the sulfamoylurea class of herbicides. Sulfamoylurea herbicides act through inhibition of branch-chain amino acid biosynthesis in plants. Orthosulfamuron′s specific mode of action is through the inhibition of the plant enzyme, acetolactate synthase, also known as acetohydroxy acid synthase (ALS/AHAS). Inhibition of ALS/AHAS blocks the branched-chain amino acid biosynthesis of valine, leucine, and isoleucine, which are involved in the plant growth process. Orthosulfamuron can be synthesized by reaction of N,N-dimethyl 2-sulfamoylchloride benzcarbamate with 2-amino-4,6-dimethoxypyrimidine in the presence of a base.

Alkalmazás

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Javasolt termékek

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Jogi információk

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Biztonsági adatok

• Tárolási osztály kódja: 11 - Combustible Solids
• WGK: WGK 3
• Lobbanási pont (F): Not applicable
• Lobbanási pont (C): Not applicable