90662

Trifluralin

certified reference material, TraceCERT^®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

• Synonym(s): 2,6-Dinitro-N,N-dipropyl-4-trifluoromethylaniline
• Empirical Formula (Hill Notation): C₁₃H₁₆F₃N₃O₄
• CAS Number: 1582-09-8
• Molecular Weight: 335.28
• Beilstein/REAXYS Number: 1893555
• MDL number: MFCD00055241
• UNSPSC Code: 41116107
• NACRES: NA.24

Properties

• grade: certified reference material; TraceCERT^®
• Quality Level: 100
• product line: TraceCERT^®
• shelf life: limited shelf life, expiry date on the label
• manufacturer/tradename: Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
• SMILES string: CCCN(CCC)c1c(cc(cc1[N+]([O-])=O)C(F)(F)F)[N+]([O-])=O
• InChI: 1S/C13H16F3N3O4/c1-3-5-17(6-4-2)12-10(18(20)21)7-9(13(14,15)16)8-11(12)19(22)23/h7-8H,3-6H2,1-2H3
• InChI key: ZSDSQXJSNMTJDA-UHFFFAOYSA-N

Description

General description

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.

Trifluralin is a pre-emergence herbicide belonging to the dinitroaniline class. It is used in various crops to control many annual types of grass and broad-leaved weeds. It is a commercially available herbicide that has been used extensively on soybeans, cotton crops, and some ornamental plants.


As per Regulation (EC) No 1107/2009, repealing the directive 91/414/EEC, trifluralin is not approved for use in the European Union. A maximum residue limit (MRL) of 0.01 mg/kg is applicable for the presence of trifluralin in fresh/frozen fruits, and tree nuts, in accordance with Regulation (EU) 2015/552.

Application

The certified reference material (CRM) is intended to be used as a calibrant for chromatography and other analytical techniques.
The trifluralin CRM may also find the following uses:

• Photocatalytic degradation of trifluralin by tin(IV) oxide-doped cuprous oxide crystals as photo-catalyst using UV-vis spectroscopy
• Sensitive electrochemical determination of trifluralin at a disposable pencil graphite electrode using differential pulse (DP) voltammetric method
• To develop and validate a QuEChERS method for trifluralin analysis in wind-eroded sediments coupled with a gas chromatography-electron capture detector(GC-ED)
• Electrochemical detection of trifluralin in untreated human plasma samples using reduced graphene oxide modified by polyethyleneimine and silver nanoparticles
• Degradation of bromoxynil and trifluralin in ultrapure and natural water solutions by direct photolysis under ultraviolet (UV) light and an advanced oxidation process combining UV and hydrogen peroxide (H₂O₂)

Recommended products

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.

Legal Information

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

Safety Information

• pictograms: GHS08,GHS07,GHS09
• signalword: Warning
• hcodes: H302,H317,H351,H410
• pcodes: P202 - P273 - P280 - P301 + P312 - P302 + P352 - P308 + P313
• Hazard Classifications: Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Skin Sens. 1
• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 2
• flash_point_f: 212.0 °F - closed cup
• flash_point_c: 100.00 °C - closed cup