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Chlorfenapyr

Manufactured by Fujifilm
Sourced in Japan

Chlorfenapyr is a chemical compound used in laboratory equipment for various analytical and research purposes. It serves as a core component in specific laboratory applications, providing a functional role in the equipment's operation. The detailed description of its intended use and applications is not available in this response, as per the provided instructions to maintain an unbiased and factual approach without extrapolation.

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2 protocols using chlorfenapyr

1

Multi-Analyte Quantification in Agrochemicals

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Analytical grade cyenopyrafen (99.8% purity) was purchased from Fujifilm Wako (Osaka, Japan), and chlorfenapyr (99.2%), indoxacarb (96.1%), spirotetramat (98.7%), and its four metabolites (BYI08330-cis-keto-hydroxy, BYI08330-mono-hydroxy, BYI08330-enol-glucoside, and BYI08330-cis-enol) (>97.9%) were obtained from Sigma-Aldrich (Burlington, MA, USA). HPLC-grade methanol, water, and acetonitrile (Burdick & Jackson, Muskegon, MI, USA) were used. The LC mobile phase was also prepared with HPLC-grade formic acid (>98%) and ammonium formate (>98%), both of which were procured from Sigma-Aldrich (Burlington, MA, USA). QuEChERS extraction packets and d-SPE tubes were received from Phenomenex (Torrance, CA, USA). A Z383K (HERMLE Labortechnik GmbH, Wehingen, Germany) refrigerated centrifuge and a CK2000 (Thmorgan, Beijing, China) shaker were used.
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2

Synthesis and Characterization of Pesticide Haptens

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Azoxystrobin, boscalid, imazalil, chlorfenapyr, isoxathion, and nitenpyram, as shown in Fig. 2 and which were of analytical grade for pesticide residue analysis, were purchased from Fujifilm Wako Pure Chemical Co. (Osaka, Japan). These pesticides were dissolved with methanol (1.0 mg/mL) and kept at 4°C until use for SPR immunosensor or with acetonitrile (1.0 mg/mL) for high performance LC (HPLC) and LC with tandem MS detectors (LC-MS/MS). These pesticides were modified with carboxylic acid as shown in Fig. 2, called haptens in this study, and synthesized as described previously. 10, 12, [19] [20] [21] [22] All of the chemicals were collected for safe disposal discard after use. Anti-Azoxystrobin monoclonal antibody (MoAb), anti-chlorfenapyr MoAb, anti-imazalil MoAb, anti-isoxathion MoAb, and anti-nitenpyram MoAb were provided from Horiba Ltd. (Kyoto, Japan). Anti-boscalid MoAb, which had been prepared in the previous study, was used. 12 Bovine serum albumin (BSA: Prod. No. A7888) was purchased from Sigma-Aldrich Co. (St. Louis, MO). Each of the haptens was conjugated to BSA as described previously. 12 All other chemicals and reagents used were of analytical grade, and purchased from Fujifilm Wako Pure Chemical Co. or Nacalai Tesque, Inc. (Kyoto, Japan).
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