Isoproturon-diflufenican mixt. | CAS#100920-69-2 | herbicide

MedKoo Cat#: 596186 | Name: Isoproturon-diflufenican mixt.

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Isoproturon-diflufenican mixt. is a herbicide.

Chemical Structure

Isoproturon-diflufenican mixt.

CAS#100920-69-2

Theoretical Analysis

MedKoo Cat#: 596186

Name: Isoproturon-diflufenican mixt.

CAS#: 100920-69-2

Chemical Formula: C31H29F5N4O3

Exact Mass: 0.0000

Molecular Weight: 600.59

Elemental Analysis: C, 62.00; H, 4.87; F, 15.82; N, 9.33; O, 7.99

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.

Bulk Inquiry

Related CAS #

No Data

Synonym

Isoproturon-diflufenican mixt.; Blutron; Blutron plus; FR 1288; FR-1288; FR1288; Javelin;

IUPAC/Chemical Name

N-(2,4-difluorophenyl)-2-(3-(trifluoromethyl)phenoxy)nicotinamide compound with 3-(4-isopropylphenyl)-1,1-dimethylurea (1:1)

InChi Key

RZSCFTDHFNHMOR-UHFFFAOYSA-N

InChi Code

InChI=1S/C19H11F5N2O2.C12H18N2O/c20-12-6-7-16(15(21)10-12)26-17(27)14-5-2-8-25-18(14)28-13-4-1-3-11(9-13)19(22,23)24;1-9(2)10-5-7-11(8-6-10)13-12(15)14(3)4/h1-10H,(H,26,27);5-9H,1-4H3,(H,13,15)

SMILES Code

O=C(NC1=CC=C(C(C)C)C=C1)N(C)C.O=C(C2=CC=CN=C2OC3=CC=CC(C(F)(F)F)=C3)NC4=CC=C(F)C=C4F

Appearance

Solid powder

Purity

>98% (or refer to the Certificate of Analysis)

Shipping Condition

Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition

Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility

Soluble in DMSO

Shelf Life

>2 years if stored properly

Drug Formulation

This drug may be formulated in DMSO

Stock Solution Storage

0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code

2934.99.9001

More Info

Instruction

View handling instruction

Preparing Stock Solutions

The following data is based on the product molecular weight 600.59 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Concentration / Solvent Volume / Mass	1 mg	5 mg	10 mg
1 mM	1.15 mL	5.76 mL	11.51 mL
5 mM	0.23 mL	1.15 mL	2.3 mL
10 mM	0.12 mL	0.58 mL	1.15 mL
50 mM	0.02 mL	0.12 mL	0.23 mL

1: Ahrens L, Daneshvar A, Lau AE, Kreuger J. Concentrations, fluxes and field calibration of passive water samplers for pesticides and hazard-based risk assessment. Sci Total Environ. 2018 May 11;637-638:835-843. doi: 10.1016/j.scitotenv.2018.05.039. [Epub ahead of print] PubMed PMID: 29758438. 2: Karas PA, Baguelin C, Pertile G, Papadopoulou ES, Nikolaki S, Storck V, Ferrari F, Trevisan M, Ferrarini A, Fornasier F, Vasileiadis S, Tsiamis G, Martin-Laurent F, Karpouzas DG. Assessment of the impact of three pesticides on microbial dynamics and functions in a lab-to-field experimental approach. Sci Total Environ. 2018 May 11;637-638:636-646. doi: 10.1016/j.scitotenv.2018.05.073. [Epub ahead of print] PubMed PMID: 29758420. 3: Yan X, Huang JW, Xu XH, Chen D, Xie XT, Tao Q, He J, Jiang JD. Enhanced and complete removal of phenylurea herbicides by combinational transgenic plant-microbial remediation. Appl Environ Microbiol. 2018 May 11. pii: AEM.00273-18. doi: 10.1128/AEM.00273-18. [Epub ahead of print] PubMed PMID: 29752264. 4: Vanraes P, Wardenier N, Surmont P, Lynen F, Nikiforov A, Van Hulle SWH, Leys C, Bogaerts A. Removal of alachlor, diuron and isoproturon in water in a falling film dielectric barrier discharge (DBD) reactor combined with adsorption on activated carbon textile: Reaction mechanisms and oxidation by-products. J Hazard Mater. 2018 May 3;354:180-190. doi: 10.1016/j.jhazmat.2018.05.007. [Epub ahead of print] PubMed PMID: 29751174. 5: Su M, Jia L, Wu X, Sun H. Residue investigation of some phenylureas and tebuthiuron herbicides in vegetables by ultra-performance liquid chromatography coupled with integrated selective accelerated solvent extraction-clean up in situ. J Sci Food Agric. 2018 Mar 24. doi: 10.1002/jsfa.9014. [Epub ahead of print] PubMed PMID: 29574757. 6: Liang X, Wang J, Wu Q, Wang C, Wang Z. Use of a hypercrosslinked triphenylamine polymer as an efficient adsorbent for the enrichment of phenylurea herbicides. J Chromatogr A. 2018 Feb 23;1538:1-7. doi: 10.1016/j.chroma.2018.01.033. PubMed PMID: 29397984. 7: Copin PJ, Chèvre N. Modelling the effects of PSII inhibitor pulse exposure on two algae in co-culture. Ecotoxicology. 2018 Mar;27(2):154-168. doi: 10.1007/s10646-017-1881-5. Epub 2017 Dec 12. PubMed PMID: 29234925. 8: Zhu X, Schroll R, Dörfler U, Chen B. Inoculation of soil with an Isoproturon degrading microbial community reduced the pool of "real non-extractable" Isoproturon residues. Ecotoxicol Environ Saf. 2018 Mar;149:182-189. doi: 10.1016/j.ecoenv.2017.11.037. Epub 2017 Nov 23. PubMed PMID: 29175344. 9: Gandar A, Laffaille P, Canlet C, Tremblay-Franco M, Gautier R, Perrault A, Gress L, Mormède P, Tapie N, Budzinski H, Jean S. Adaptive response under multiple stress exposure in fish: From the molecular to individual level. Chemosphere. 2017 Dec;188:60-72. doi: 10.1016/j.chemosphere.2017.08.089. Epub 2017 Aug 19. PubMed PMID: 28869847. 10: Wang Y, Li H, Feng G, Du L, Zeng D. Biodegradation of diuron by an endophytic fungus Neurospora intermedia DP8-1 isolated from sugarcane and its potential for remediating diuron-contaminated soils. PLoS One. 2017 Aug 15;12(8):e0182556. doi: 10.1371/journal.pone.0182556. eCollection 2017. PubMed PMID: 28809955; PubMed Central PMCID: PMC5557362. 11: Le TDH, Scharmüller A, Kattwinkel M, Kühne R, Schüürmann G, Schäfer RB. Contribution of waste water treatment plants to pesticide toxicity in agriculture catchments. Ecotoxicol Environ Saf. 2017 Nov;145:135-141. doi: 10.1016/j.ecoenv.2017.07.027. Epub 2017 Jul 18. PubMed PMID: 28732296. 12: Esteves SM, Keck F, Almeida SFP, Figueira E, Bouchez A, Rimet F. Can we predict diatoms herbicide sensitivities with phylogeny? Influence of intraspecific and interspecific variability. Ecotoxicology. 2017 Oct;26(8):1065-1077. doi: 10.1007/s10646-017-1834-z. Epub 2017 Jul 6. PubMed PMID: 28685416. 13: Gaullier C, Dousset S, Billet D, Baran N. Is pesticide sorption by constructed wetland sediments governed by water level and water dynamics? Environ Sci Pollut Res Int. 2017 May 15. doi: 10.1007/s11356-017-9123-1. [Epub ahead of print] PubMed PMID: 28508331. 14: Gorito AM, Ribeiro AR, Almeida CMR, Silva AMT. A review on the application of constructed wetlands for the removal of priority substances and contaminants of emerging concern listed in recently launched EU legislation. Environ Pollut. 2017 Aug;227:428-443. doi: 10.1016/j.envpol.2017.04.060. Epub 2017 May 6. Review. PubMed PMID: 28486186. 15: Boucheloukh H, Remache W, Parrino F, Sehili T, Mechakra H. The effect of natural iron oxide and oxalic acid on the photocatalytic degradation of isoproturon: a kinetics and analytical study. Photochem Photobiol Sci. 2017 May 17;16(5):759-765. doi: 10.1039/c6pp00441e. PubMed PMID: 28345701. 16: Dollinger J, Dagès C, Voltz M. Using fluorescent dyes as proxies to study herbicide removal by sorption in buffer zones. Environ Sci Pollut Res Int. 2017 Apr;24(12):11752-11763. doi: 10.1007/s11356-017-8703-4. Epub 2017 Mar 23. PubMed PMID: 28337625. 17: Vanraes P, Ghodbane H, Davister D, Wardenier N, Nikiforov A, Verheust YP, Van Hulle SWH, Hamdaoui O, Vandamme J, Van Durme J, Surmont P, Lynen F, Leys C. Removal of several pesticides in a falling water film DBD reactor with activated carbon textile: Energy efficiency. Water Res. 2017 Jun 1;116:1-12. doi: 10.1016/j.watres.2017.03.004. Epub 2017 Mar 6. PubMed PMID: 28292675. 18: Eissa S, Zourob M. Selection and Characterization of DNA Aptamers for Electrochemical Biosensing of Carbendazim. Anal Chem. 2017 Mar 7;89(5):3138-3145. doi: 10.1021/acs.analchem.6b04914. Epub 2017 Feb 10. PubMed PMID: 28264568. 19: Yotsova EK, Stefanov MA, Dobrikova AG, Apostolova EL. Different sensitivities of photosystem II in green algae and cyanobacteria to phenylurea and phenol-type herbicides: effect on electron donor side. Z Naturforsch C. 2017 Jul 14;72(7-8):315-324. doi: 10.1515/znc-2016-0089. PubMed PMID: 28258977. 20: Jeong Y, Schäffer A, Smith K. Equilibrium partitioning of organic compounds to OASIS HLB(®) as a function of compound concentration, pH, temperature and salinity. Chemosphere. 2017 May;174:297-305. doi: 10.1016/j.chemosphere.2017.01.116. Epub 2017 Jan 26. PubMed PMID: 28183055.