41342

Isoprocarb

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

• Synonym(s): 2-Isopropylphenyl N-methylcarbamate
• Empirical Formula (Hill Notation): C₁₁H₁₅NO₂
• CAS Number: 2631-40-5
• Molecular Weight: 193.24
• Beilstein: 1875020
• MDL number: MFCD00053078
• UNSPSC Code: 41116107
• NACRES: NA.24

Properties

• grade: certified reference material; TraceCERT^®
• Quality Level: 300
• product line: TraceCERT^®
• shelf life: limited shelf life, expiry date on the label
• manufacturer/tradename: Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
• format: neat
• shipped in: wet ice
• storage temp.: 2-8°C
• SMILES string: CNC(=O)Oc1ccccc1C(C)C
• InChI: 1S/C11H15NO2/c1-8(2)9-6-4-5-7-10(9)14-11(13)12-3/h4-8H,1-3H3,(H,12,13)
• InChI key: QBSJMKIUCUGGNG-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

Isoprocarb is one of the most important carbamate insecticides that is used against a variety of sucking and chewing insects for plants in tropical and subtropical regions, notably rice and cotton leafhopper. It functions as an acetylcholinesterase (AChE) inhibitor and acts by contact and stomach poisoning.

Isoprocarb is not approved for use in European Union (EU) according to Regulation (EC) No 1107/2009 (repealing Directive 91/414/EEC). However, a default MRL of 0.01 mg/kg is set according to Art 18(1)(b) Reg 396 / 2005.

Application

It is intended to be used as a certified reference material (CRM) for calibration in chromatography and other analytical techniques. Isoprocarb CRM may also find its use as described below:

• To examine the toxicity of isoprocarb on Eisenia fetida, at lethal and sublethal concentrations, and elucidate its toxic modes of action as well as biochemical and detoxification mechanisms
• Study the binding interaction of isoprocarb and sodium 2-isopropylphenate with bovine serum albumin (BSA) by spectrofluorimetry under simulated physiological conditions
• To develop an analytical method for the detection and quantitation of 3-hydroxycarbofuran, 3-ketocarbofuran, carbofuran, carbosulfan, and isoprocarb using micellar electrokinetic chromatography coupled with a UV-Vis detector
• To develop an electrochemical multianalyte screening method for the detection of carbaryl, carbofuran, isoprocarb, and fenobucarb applied to grains samples (durum wheat, soft wheat, and maize)
• To investigate the effect of salt additives on cloud point extraction (CPE) of isoprocarb and promecarb followed by their residue analysis in fruit juices, vegetable juices, and local wines using HPLC

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: GHS07,GHS09
• Signal Word: Warning
• Hazard Statements: H302,H410
• Precautionary Statements: P264 - P270 - P273 - P301 + P312 - P391 - P501
• Hazard Classifications: Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 3
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable